2,082 Clinical Project Management jobs in the United States

**Position Overview:**
IQVIA is seeking an experienced Associate Clinical Project Management Director/Trial Delivery Manager (TDM) to lead and coordinate global and regional clinical trial management activities. This role ensures the successful planning, execution, and closure of clinical trials, whether internally managed or outsourced. The TDM will serve as a key member of the Study Management Team (SMT), supporting trial leaders and interfacing with internal and external stakeholders to ensure compliance, quality, and timely delivery of trial milestones.
**Key Responsibilities:**
**Trial Oversight & Management**
+ Lead the Study Management Team and provide regular updates on trial deliverables.
+ Ensure real-time tracking and documentation of trial progress.
+ Maintain inspection-readiness throughout the trial lifecycle.
+ Act as the primary contact for country and regional staff and internal teams.
+ Partner with Global Trial Leads to oversee central trial activities from start-up to close-out.
+ Escalate and resolve trial issues and contribute to CAPA processes.
**Site & Vendor Coordination**
+ Support site selection and feasibility assessments.
+ Monitor enrollment commitments and ensure recruitment plans are in place.
+ Oversee selected vendors and review related deliverables and invoices.
+ Coordinate with vendors such as IVRS, Central Labs, ePRO, Imaging, Translation, and Ancillary Supplies.
**Documentation & Compliance**
+ Create and maintain trial-specific documents (e.g., Monitoring Guidelines, ICFs, Blinding Plans).
+ Ensure timely filing, archiving, and retention of trial documents.
+ Provide central documents for regulatory submissions.
+ Support Health Authority inspections and internal audits.
**Training & Meetings**
+ Develop and deliver trial-specific training materials.
+ Coordinate and participate in Investigator Meetings.
**Budget & Financial Oversight**
+ Establish country budgets and monitor actuals vs. forecast.
+ Understand Out-of-Pocket (OOP) and FTE cost drivers.
**Qualifications:**
**Education:**
+ Bachelor's degree in Life Sciences (Biology, Chemistry, Biochemistry, Nursing, Pharmacy) or equivalent.
**Experience:**
+ **Level 2 (Advanced):** Minimum 8 years of experience, with proven leadership in complex trials at a large pharmaceutical company.
**Skills & Competencies:**
+ Strong knowledge of ICH-GCP and local regulatory requirements.
+ Proven ability to lead cross-functional teams and manage global trials.
+ Excellent communication, decision-making, and analytical skills.
+ Proficiency in Microsoft Office, CTMS, TMF, and other clinical systems.
+ Experience in virtual team coordination and stakeholder engagement.
+ Ability to manage ambiguity and drive solutions proactively.
**Preferred Attributes:**
+ Monitoring or data management experience.
+ Experience in budget planning and financial oversight.
+ Ability to mentor junior CTMs and lead special initiatives or task forces.
+ Therapeutic area expertise and ability to act as protocol expert.
**Metrics & KPIs:**
Performance will be measured according to the Quality Oversight Plan (QOP) and trial-specific deliverables.
*This is a remote home-based role that may require some travel
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. potential base pay range for this role, when annualized, is $93,100.00 - $285,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Position Overview:**
IQVIA is seeking an experienced Associate Clinical Project Management Director/Trial Delivery Manager (TDM) to lead and coordinate global and regional clinical trial management activities. This role ensures the successful planning, execution, and closure of clinical trials, whether internally managed or outsourced. The TDM will serve as a key member of the Study Management Team (SMT), supporting trial leaders and interfacing with internal and external stakeholders to ensure compliance, quality, and timely delivery of trial milestones.
**Key Responsibilities:**
**Trial Oversight & Management**
+ Lead the Study Management Team and provide regular updates on trial deliverables.
+ Ensure real-time tracking and documentation of trial progress.
+ Maintain inspection-readiness throughout the trial lifecycle.
+ Act as the primary contact for country and regional staff and internal teams.
+ Partner with Global Trial Leads to oversee central trial activities from start-up to close-out.
+ Escalate and resolve trial issues and contribute to CAPA processes.
**Site & Vendor Coordination**
+ Support site selection and feasibility assessments.
+ Monitor enrollment commitments and ensure recruitment plans are in place.
+ Oversee selected vendors and review related deliverables and invoices.
+ Coordinate with vendors such as IVRS, Central Labs, ePRO, Imaging, Translation, and Ancillary Supplies.
**Documentation & Compliance**
+ Create and maintain trial-specific documents (e.g., Monitoring Guidelines, ICFs, Blinding Plans).
+ Ensure timely filing, archiving, and retention of trial documents.
+ Provide central documents for regulatory submissions.
+ Support Health Authority inspections and internal audits.
**Training & Meetings**
+ Develop and deliver trial-specific training materials.
+ Coordinate and participate in Investigator Meetings.
**Budget & Financial Oversight**
+ Establish country budgets and monitor actuals vs. forecast.
+ Understand Out-of-Pocket (OOP) and FTE cost drivers.
**Qualifications:**
**Education:**
+ Bachelor's degree in Life Sciences (Biology, Chemistry, Biochemistry, Nursing, Pharmacy) or equivalent.
**Experience:**
+ **Level 2 (Advanced):** Minimum 8 years of experience, with proven leadership in complex trials at a large pharmaceutical company.
**Skills & Competencies:**
+ Strong knowledge of ICH-GCP and local regulatory requirements.
+ Proven ability to lead cross-functional teams and manage global trials.
+ Excellent communication, decision-making, and analytical skills.
+ Proficiency in Microsoft Office, CTMS, TMF, and other clinical systems.
+ Experience in virtual team coordination and stakeholder engagement.
+ Ability to manage ambiguity and drive solutions proactively.
**Preferred Attributes:**
+ Monitoring or data management experience.
+ Experience in budget planning and financial oversight.
+ Ability to mentor junior CTMs and lead special initiatives or task forces.
+ Therapeutic area expertise and ability to act as protocol expert.
**Metrics & KPIs:**
Performance will be measured according to the Quality Oversight Plan (QOP) and trial-specific deliverables.
*This is a remote home-based role that may require some travel
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. potential base pay range for this role, when annualized, is $93,100.00 - $285,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Position Overview:**
IQVIA is seeking an experienced Associate Clinical Project Management Director/Trial Delivery Manager (TDM) to lead and coordinate global and regional clinical trial management activities. This role ensures the successful planning, execution, and closure of clinical trials, whether internally managed or outsourced. The TDM will serve as a key member of the Study Management Team (SMT), supporting trial leaders and interfacing with internal and external stakeholders to ensure compliance, quality, and timely delivery of trial milestones.
**Key Responsibilities:**
**Trial Oversight & Management**
+ Lead the Study Management Team and provide regular updates on trial deliverables.
+ Ensure real-time tracking and documentation of trial progress.
+ Maintain inspection-readiness throughout the trial lifecycle.
+ Act as the primary contact for country and regional staff and internal teams.
+ Partner with Global Trial Leads to oversee central trial activities from start-up to close-out.
+ Escalate and resolve trial issues and contribute to CAPA processes.
**Site & Vendor Coordination**
+ Support site selection and feasibility assessments.
+ Monitor enrollment commitments and ensure recruitment plans are in place.
+ Oversee selected vendors and review related deliverables and invoices.
+ Coordinate with vendors such as IVRS, Central Labs, ePRO, Imaging, Translation, and Ancillary Supplies.
**Documentation & Compliance**
+ Create and maintain trial-specific documents (e.g., Monitoring Guidelines, ICFs, Blinding Plans).
+ Ensure timely filing, archiving, and retention of trial documents.
+ Provide central documents for regulatory submissions.
+ Support Health Authority inspections and internal audits.
**Training & Meetings**
+ Develop and deliver trial-specific training materials.
+ Coordinate and participate in Investigator Meetings.
**Budget & Financial Oversight**
+ Establish country budgets and monitor actuals vs. forecast.
+ Understand Out-of-Pocket (OOP) and FTE cost drivers.
**Qualifications:**
**Education:**
+ Bachelor's degree in Life Sciences (Biology, Chemistry, Biochemistry, Nursing, Pharmacy) or equivalent.
**Experience:**
+ **Level 2 (Advanced):** Minimum 8 years of experience, with proven leadership in complex trials at a large pharmaceutical company.
**Skills & Competencies:**
+ Strong knowledge of ICH-GCP and local regulatory requirements.
+ Proven ability to lead cross-functional teams and manage global trials.
+ Excellent communication, decision-making, and analytical skills.
+ Proficiency in Microsoft Office, CTMS, TMF, and other clinical systems.
+ Experience in virtual team coordination and stakeholder engagement.
+ Ability to manage ambiguity and drive solutions proactively.
**Preferred Attributes:**
+ Monitoring or data management experience.
+ Experience in budget planning and financial oversight.
+ Ability to mentor junior CTMs and lead special initiatives or task forces.
+ Therapeutic area expertise and ability to act as protocol expert.
**Metrics & KPIs:**
Performance will be measured according to the Quality Oversight Plan (QOP) and trial-specific deliverables.
*This is a remote home-based role that may require some travel
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. potential base pay range for this role, when annualized, is $93,100.00 - $285,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
R&D Operations
**Job Sub** **Function:**
Clinical Trial Project Management
**Job Category:**
Professional
**All Job Posting Locations:**
Spring House, Pennsylvania, United States of America
**Job Description:**
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at are searching for the best talent for a **Manager, Clinical Trial Project Management** to be responsible for the creation and management of a subset of studies within our Medical Affairs Deliver Unit Portfolio. You will collect, consolidate, and report budget, timeline and FTE actuals vs. plan and will identify potential issues for the trial through active management of the study schedule. The position may be located **Beerse, Belgium; Leiden, Netherlands; Madrid, Spain; High Wycombe, UK; Cork, Ireland; Warsaw, Poland; or Spring House, United States.** The position is Hybrid (3 days onsite weekly).
**You will be responsible for:**
+ Creating, managing, and maintaining study schedules in PLW + For company sponsored and collaborative studies; creating initial study costing and support initial OOPS management up till FPI.
+ Assuring Clinical timelines in PLW align to mCTMS and to latest assumptions. Ensuring proper resource demand is reflected
+ Developing scenarios in PLW for budget, timeline, and FTE forecasting, while generating situational operational scenarios.
+ Collecting, consolidating, and reporting financial, timeline and resource data for governance approvals and external funding partnerships. Managing scope control, FTE and OOP variances. + Providing necessary Portfolio Data Insights to the TA leads
+ Providing necessary Portfolio Data Insights to the TA leads
+ Providing support to Finance, Business Partners and Commercial Stakeholders
**Additional Responsibilities may Include:**
+ Mentoring and supporting onboarding of new team members, particularly those in Trial Management.
+ Fostering employee engagement, inclusion, and Credo Behaviors.
**Principal Relationships:**
Internal: Trial Delivery Leader, Trial Delivery Manager, Program Delivery Leaders, Clinical Trial Assistants, DAS Leaders, Trial Management Directors, representatives of Delivery Operations, representatives of other GD and non-GD Functions and Clinical and Project Management Teams
**Qualifications /Requirements:**
+ BS degree or equivalent, preferred areas of study include Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy).
+ Minimum of 6 years of experience in Pharmaceutical, Healthcare or related industries.
+ Experience in and knowledge of the pharmaceutical development process
+ Clinical research operational knowledge and experience across multiple phases of studies (Phase I-IV); must have the ability to manage all aspects of execution of a clinical trial.
+ Experience in Project Management, preferably within Research & Development.
+ Knowledge of Project Management Systems, Methodologies & Tools.
+ Must possess excellent leadership skills and proven ability to foster team productivity and cohesiveness. Experience of leading without authority and in muti-functional matrixed and global environments. Excellent decision-making, analytical and strong financial management skills are essential to this position. Operates and executes with limited supervision. Experience mentoring/coaching others.
+ Strong project planning/management, communication and presentation skills are required.
+ Travel up to 10% of the time, defined by business needs.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
+ Belgium, Ireland, Netherlands, Spain, Poland- Requisition Number: R-
+ United Kingdom - Requisition Number: R-
+ United States - Requisition Number: R-
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
**For United States applicants only:**
The anticipated base pay range for this position is $115,000 to $197,800 (USD).
The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/ performance year. Bonuses are awarded at the Company's discretion on an individual basis.
Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
Employees are eligible for the following time off benefits:
- Vacation - up to 120 hours per calendar year
+ Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year
- Holiday pay, including Floating Holidays - up to 13 days per calendar year
- Work, Personal and Family Time - up to 40 hours per calendar year
For additional general information on company benefits, please go to: compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
**#LI-Hybrid**
**The anticipated base pay range for this position is :**
115,000 - 197,800 USD
Additional Description for Pay Transparency:

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at

Job Function:

R&D Operations

Job Sub Function:

Clinical Trial Project Management

Job Category:

Professional

All Job Posting Locations:

Spring House, Pennsylvania, United States of America

Job Description:

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at are searching for the best talent for a Manager, Clinical Trial Project Management to be responsible for the creation and management of a subset of studies within our Medical Affairs Deliver Unit Portfolio. You will collect, consolidate, and report budget, timeline and FTE actuals vs. plan and will identify potential issues for the trial through active management of the study schedule. The position may be located Beerse, Belgium; Leiden, Netherlands; Madrid, Spain; High Wycombe, UK; Cork, Ireland; Warsaw, Poland; or Spring House, United States. The position is Hybrid (3 days onsite weekly).

You will be responsible for:

• Creating, managing, and maintaining study schedules in PLW + For company sponsored and collaborative studies; creating initial study costing and support initial OOPS management up till FPI.
• Assuring Clinical timelines in PLW align to mCTMS and to latest assumptions. Ensuring proper resource demand is reflected
• Developing scenarios in PLW for budget, timeline, and FTE forecasting, while generating situational operational scenarios.
• Collecting, consolidating, and reporting financial, timeline and resource data for governance approvals and external funding partnerships. Managing scope control, FTE and OOP variances. + Providing necessary Portfolio Data Insights to the TA leads
• Providing necessary Portfolio Data Insights to the TA leads
• Providing support to Finance, Business Partners and Commercial Stakeholders

Additional Responsibilities may Include:

• Mentoring and supporting onboarding of new team members, particularly those in Trial Management.
• Fostering employee engagement, inclusion, and Credo Behaviors.

Principal Relationships:

Internal: Trial Delivery Leader, Trial Delivery Manager, Program Delivery Leaders, Clinical Trial Assistants, DAS Leaders, Trial Management Directors, representatives of Delivery Operations, representatives of other GD and non-GD Functions and Clinical and Project Management Teams

Qualifications /Requirements:

• BS degree or equivalent, preferred areas of study include Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy).
• Minimum of 6 years of experience in Pharmaceutical, Healthcare or related industries.
• Experience in and knowledge of the pharmaceutical development process
• Clinical research operational knowledge and experience across multiple phases of studies (Phase I-IV); must have the ability to manage all aspects of execution of a clinical trial.
• Experience in Project Management, preferably within Research & Development.
• Knowledge of Project Management Systems, Methodologies & Tools.
• Must possess excellent leadership skills and proven ability to foster team productivity and cohesiveness. Experience of leading without authority and in muti-functional matrixed and global environments. Excellent decision-making, analytical and strong financial management skills are essential to this position. Operates and executes with limited supervision. Experience mentoring/coaching others.
• Strong project planning/management, communication and presentation skills are required.
• Travel up to 10% of the time, defined by business needs.

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

• Belgium, Ireland, Netherlands, Spain, Poland- Requisition Number: R-
• United Kingdom - Requisition Number: R-
• United States - Requisition Number: R-

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

For United States applicants only: 

The anticipated base pay range for this position is $115,000 to $197,800 (USD).  

The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/ performance year. Bonuses are awarded at the Company’s discretion on an individual basis.  

Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.  

Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).  

Employees are eligible for the following time off benefits: 

- Vacation - up to 120 hours per calendar year  

• Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year 

- Holiday pay, including Floating Holidays - up to 13 days per calendar year  

- Work, Personal and Family Time - up to 40 hours per calendar year  

For additional general information on company benefits, please go to: compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market. 

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.  

#LI-Hybrid

The anticipated base pay range for this position is :

115,000 - 197,800 USD

Additional Description for Pay Transparency:

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
Envision spending your summer working with energetic colleagues and inspirational leaders, all while gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie Interns.
The Clinical Supply Project Management intern will spend the summer with Clinical Drug Supply Management. This department is responsible for understanding the clinical development plans, translating that into clinical drug supply requirements, and planning the manufacturing, packaging, and distribution of clinical supplies to ensure smooth clinical study conduct and zero disruptions to clinical subjects participating in AbbVie clinical trials. It is a fast paced and highly dynamic business with a focus on agility and flawless execution to enable our RD pipeline.
Key Responsibilities Include:
+ Understanding the major factors that influence demand for clinical supplies and the different strategies utilized to ensure uninterrupted supply.
+ Using available data to look for trends and opportunities to improve processes and decision making.
+ Analyzing business processes to understand current requirements and workflows with the aim of helping colleagues identify opportunities for efficiency
Qualifications
Minimum Qualifications
+ Currently enrolled in university, pursuing a Bachelor's in Supply Chain, Project Management, Engineering or other related field.
+ Must be enrolled in university for at least one semester following the internship
+ Expected graduation date between December 2026 - June 2027
Preferred Qualifications
+ Exposure to data analytics, design of experiments, supply chain, manufacturing, planning, scheduling, forecasting, Lean Six-Sigma concepts
Additional Information
+ Competitive pay
+ Relocation support for eligible students
+ Select wellness benefits and paid holiday / sick time
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$20.3 - $36.5

Healthcare Project Team at Takeda summary:

The General Superintendent oversees the field operations and execution of a $500M+ healthcare facility construction project, ensuring safety, timely delivery, budget adherence, and quality standards. This role requires extensive experience in large-scale healthcare construction, knowledge of hospital systems and regulations, and strong leadership to manage subcontractors and field teams. The position demands over 15 years in healthcare construction, direct project team supervision, and relevant educational qualifications.

Insight Global is looking for a General Superintendent to join a large client of ours in the construction industry. The General Superintendent is responsible for the overall field operations and execution of a $500M+ healthcare facility construction project. This role ensures the project is delivered safely, on time, within budget, and to the highest quality standards. The ideal candidate will have extensive experience managing large-scale healthcare construction projects, deep knowledge of hospital systems and regulatory requirements, and strong leadership skills to coordinate multiple subcontractors and field teams.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy:
Required Skills & Experience
• 15+ years of experience in healthcare construction industry
• Experience managing large (500 million + healthcare construction projects)
• 8 years of direct supervision of project teams
• Bachelor's Degree in any related field
Osha 30
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

Keywords:

healthcare construction, project management, construction superintendent, large-scale projects, hospital systems, regulatory compliance, field operations, subcontractor coordination, safety management, budget control

Overview

The 50+ person growing studio is seeking a Healthcare Project Architect (licensure preferred) to join their growing collaborative firm! (The position could be located in either the LA or San Diego office. Fully remote work options are available, but candidates must be based in Southern California.)

Mid-size Los Angeles & San Diego Architecture + Interiors studio has received acclaim for its award-winning healthcare designs for clients including Kaiser Permanente, UCLA, UCI, and Children’s Hospital Los Angeles. Voted as one of the “Best Places to Work” for healthcare, designers and architects at this firm never leave! This is one of our first clients and candidates love it here. From landmark medical campuses to intimate imaging suites, the studio designs exceptional environments that promote healing while meeting the healthcare industry's planning, efficiency and technical demands. Their studio's architectural ingenuity, technical expertise, and attention to detail consistently place their projects at the forefront of cutting-edge design. (Note: Opportunity for fully remote available with occasional travel to job sites & critical meetings.)

Overall Responsibilities

• Support Management and running of architectural projects with the firm
• Ability, skills, and motivation to act as independent project architect

Job Responsibilities

• Assist team in business development efforts to win new projects as required
• Work closely with Project Manager to establish project plan, milestone schedule, and staffing
• Work closely with Project Manager to follow both construction and internal project budgets
• Work in all project phases from programming through project closeout
• Develop project cartoon set for assigned projects
• May conduct client design meetings
• May conduct team meetings
• Responsible for code compliancy as it relates to Title 24, ADA, Energy Codes and Life Safety in relation to planning and documentation. Mentor and train staff on code compliancy.
• Work closely with the Design Team to execute the vision and spirit of the design for assigned projects and ensuring that constructability methods and technologies are explored and implemented
• Monitor project schedules and tasks while enforcing office standards and budgeting hours per fee contracts
• Keep abreast of technological developments and understand design and technical criteria such as new codes, new design concepts, computer applications, drafting methods, etc.
• Lead project team through documentation, modeling, quality control, and consultant coordination
• Perform building systems selection, evaluation, and detailing
• Proficiency with development of building envelope details and interior building systems coordination
• Understand, lead and review the development of project manuals
• Schedule the work and oversee its production
• Ensure each project complies with the client’s needs, facility standards, and the company quality standards, delivering projects on-time and on-budget
• Perform ongoing document quality control reviews
• Motivate and mentor junior staff ensuring their professional and technical development and leading by example
• Understand construction sequencing and constructability
• Coordinate work and maintain professional relationships with clients, contractors, agencies, inspectors, and consultants.
• Perform in all aspects of the CA phase
• Responsible for quality control of documents
• Provide exceptional customer service to our clients and build strong relationships based on trust, value, and expertise
• Identify ways to innovate and improve the accuracy and efficiency of our processes

Qualifications

• Licensed Architect preferred
• 10+ Years of experience preferred
• Candidate must have acute healthcare experience
• Ability to manage and appraise own working practices
• Good organizational skills and ability to work under own initiative
• Exceptional Revit skills

Position: Healthcare Project Architect

Location: Los Angeles, CA

Hybrid Schedule: 1-2 days in office weekly (Flexible)

About Us: We are a nationally recognized architecture and design practice with a reputation for delivering innovative, human-centered solutions in healthcare and beyond. Our teams are trusted to design and deliver some of the most complex and high-profile facilities in the country, shaping environments that improve lives and transform communities. Recognized for excellence in both design and culture, we offer the resources of a top-tier firm with the agility and collaborative spirit of a close-knit studio.

The Position: We are seeking a highly skilled Healthcare Project Architect to join our Los Angeles team. This role focuses on leading the design and technical delivery of large-scale healthcare projects, ranging from advanced cancer centers to behavioral health facilities and major hospital expansions. This is a hybrid position, with only 1–2 in-office days per week, offering a flexible schedule rarely found in the industry.

What You’ll Do:

• Lead project design and technical systems from schematic design through construction administration.
• Manage and mentor project team members, fostering quality, accuracy, and collaboration.
• Serve as a discipline leader on complex, multi-million-dollar healthcare projects.
• Conduct code research, material/product studies, and maintain documentation throughout all project phases.
• Oversee project schedules, progress reports, and client coordination.
• Collaborate with cross-discipline leaders to ensure seamless integration of design solutions.
• Represent the firm at client, project, and construction meetings, including site visits.

What We’re Looking For:

• Bachelor’s degree in Architecture required; licensure strongly preferred.
• 10+ years of professional experience in healthcare architecture, including significant HCAi/OSHP expertise.
• Strong technical knowledge spanning schematic design through project close-out.
• Proven ability to coordinate across disciplines, lead teams, and mentor staff.
• LEED accreditation preferred.
• Excellent communication, organizational, and leadership skills.
• Proficiency with Revit and related design technologies.
• A detail-oriented, motivated, and flexible professional with a passion for healthcare design.

What’s Offered:

• Salary: $110,000 – $150,000 annually (DOE)
• Competitive performance Bonuses
• Full suite of benefits: Medical, Dental, Vision
• 401K with company match
• Generous PTO, vacation, sick days, and personal time
• 10+ paid holidays annually
• Hybrid Work Schedule: (1–2 days in-office/weekly - super flexible!)
• License and certification reimbursement, continuing education support
• Additional perks, incentives, and professional growth opportunities

Apply Today: Apply directly to this ad with your resume/work to be considered. Recommended: Email resume/work to for a prompt review and consideration.

Explore More Active Opportunities: We encourage you to continue exploring at BancroftSP.com/Careers/ and following Bancroft Staffing Partners via LinkedIn. We’re consistently updating our network with new and exciting opportunities, market insights, trends, and recruiter tips.

Equal Opportunity Statement: Bancroft Staffing Partners is an equal opportunity employer. We celebrate diversity & are committed to creating an inclusive environment for all employees & candidates, regardless of race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.