5,059 Study Management jobs in the United States

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:

• Career development with an international company where you can grow the career you dream of
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year
• An excellent retirement savings plan with high employer contribution
• Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists

Are you a strategic leader with a passion for clinical research and operational excellence? Join our high-impact team as a Senior Director, Clinical Study Management overseeing a global portfolio of 100+ clinical studies across six business units in our Medical Devices division.

Why Join Us? Lead a mission-driven portfolio that impacts patient lives globally. Work in a collaborative, innovative, and growth-oriented environment. Gain executive visibility and influence across multiple business units.

What You'll Work On

• Lead the project management of global clinical trials with budgets exceeding $100MM.
• Influence study design allowing for seamless study execution.
• Drive strategic execution of clinical and regulatory goals across diverse therapeutic areas.
• Manage timelines, budgets, and resources across a complex, multi-BU portfolio.
• Collaborate with global teams to ensure regulatory compliance and operational excellence.
• Mentor and develop a high-performing team of project managers and clinical professionals.
• Operational Excellence Through Milestone Management: Oversee 400+ annual study milestones with a continuous improvement mindsetleveraging data and feedback loops to enhance efficiency, predictability, and execution quality.
• Upstream Clinical Protocol Influence: Engage early in protocol development to ensure operational feasibility, minimize downstream challenges, and optimize business outcomes.
• Strategic Business Partnership: Serve as a strategic partner to the business by aligning clinical operations with long-term regulatory and reimbursement goals. Influence study design to support future approvals and market access.
• Strong Understanding of the Global Regulatory Landscape: Bring deep knowledge of international regulatory requirements to guide operational decisions.

Qualifications

• Bachelor's degree in life sciences required
• Advanced degree preferred
• 7+ years of experience required leading large-scale, pre-market clinical trials in the medical device industry
• Proven success required managing global studies and large budgets
• Experience in vascular or cardiovascular devices is a plus
• Strong leadership, communication, and cross-functional collaboration skills

The base pay for this position is $16,700.00 433,300.00. In specific locations, the pay range may vary from the range posted.

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.

The Associate Director, Clinical Study Management, will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required. This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in our California office to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration. The successful candidate will work closely with cross-functional Clinical Research & Development teams to ensure successful completion of studies within timelines and budget, with a focus on exquisite quality to support operational excellence and world class inhouse clinical study management.

This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our California or New Jersey offices to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration.

You are collaborative, solutions oriented, flexible and have global clinical operational experience, with a passion for excellence in advancing patient care in oncology.

• Team leader and builder, who manages clinical trial deliverables, timelines, and budgets per the Clinical Development and Operational Plans
• Works with minimal oversight from the Clinical Operations Senior Director or Director, in collaboration with Clinical Study Management teams and Clinical Research and Development functional teams
• Demonstrate broad understanding of therapeutic and clinical drug development expertise to influence study design and program-level decisions
• Provide direction to cross-functional study teams to ensure successful study execution Ensure that clinical studies are conducted following approved protocols, FDA Regulations, ICH-GCP, EMA, PMDA, other relevant regulations, directives, and guidelines, and company procedures and quality documents
• Oversee risk identification, assessment, and mitigation strategies to ensure patient safety and data integrity
• Responsible for the implementation of processes and systems that will facilitate inspection readiness throughout the lifecycle of the trial.
• Oversee the preparation and maintenance of detailed clinical trial project timelines
• Manage ancillary (non CRO) vendor relationships and performance to ensure that clinical studies are completed following contract specifications of time, cost and quality.
• Work with finance, legal, and external vendors to ensure the assigned studies are meeting the target milestones
• Provide regular updates on study progress to stakeholders (e.g., Clinical Operations, Project & Portfolio Management, Clinical Research)
• Ensure that all study-related documents are accurate, complete, timely and filed appropriately in all clinical (Veeva TMF), regulatory, safety and finance systems.
• Responsible for hiring, performance management, career development, and providing mentorship to Clinical Study Management personnel.
• Contribute to initiatives and projects adding value to Eikon Therapeutics

• Minimum of 10 years of related experience with a Bachelor's degree or 8 years and a post-graduate degree.
• Experience leading large, global clinical trials, preferably in oncology
• In-depth knowledge of ICH-GCP, EMA guidelines and other relevant regulations and guidelines.
• Proven ability to manage clinical studies within timelines and budgets while maintaining high quality standards and patient safety.
• Strong leadership and communication skills, with a demonstrated ability to work collaboratively with cross-functional teams.
• Experience with management of the budget, resources, headcount, processes and controls, productivity, quality and project delivery.
• High sense of accountability and urgency to prioritize deliverables.
• Growth mindset and capable of working independently.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:

• 401k plan with company matching
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
• Mental health and wellness benefits
• Weeklong summer and winter holiday shutdowns
• Generous paid time off and holiday policies
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
• Enhanced parental leave benefit
• Daily subsidized lunch program when on-site

The expected salary range for this role is $183,000 to $199,500 depending on skills, competency, and the market demand for your expertise.

Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment. We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.

Description Clinical Project Manager II - Biomarker Study Management (Sponsor-Dedicated | Remote)Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHEREWhy Syneos HealthWe are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong. Job ResponsibilitiesClinical Project Manager II - Biomarker Study Management(Sponsor-Dedicated | Remote)We're hiring a Clinical Project Manager II with a strong background in biomarker study operations to join our sponsor-dedicated team. This fully remote role gives you the opportunity to drive the success of global clinical trials by leading biomarker and bioanalytical strategy from start to finish.You'll be a key player in bringing together cross-functional teams, vendors, and internal stakeholders to ensure biological samples are collected, managed, and analyzed to the highest standards. What You'll Do: Lead Biomarker Study OperationsOversee biomarker and bioanalytical activities across Sponsor and Collaborative programsServe as the operational point of contact for all biomarker-related processesWork closely with clinical study teams (Phases 1-4) to integrate biomarker strategies into broader clinical development plansPlan and manage the collection, tracking, and analysis of biological specimensAdvise study teams on best practices for sample management and logisticsDrive Clinical Project DeliveryLead cross-functional teams through the full clinical trial lifecycle, from start-up to closeoutEnsure studies stay on track with respect to timelines, budget, scope, and qualityAct as the main liaison between the sponsor and study partnersMonitor and manage project financials, ensuring fiscal responsibilityProactively identify and resolve operational issues and risksEnsure Operational ExcellenceMaintain high-quality documentation, including Trial Master File (TMF) accuracy and completenessKeep study systems and databases current and audit-readyPrepare project reports and updates for sponsors and internal stakeholdersPlan and facilitate internal and external meetingsSupport inspection readiness and regulatory compliance throughout the projectSkills and Experience You Bring:Significant experience managing biomarker studies and external vendors required!Strong understanding of biomarker and bioanalytical strategies in a clinical trial settingProven ability to coordinate complex sample collection and analysis workflowsExpertise in supporting study teams with sample logistics and operational planningBachelor's degree in Life Sciences, Medicine, Pharmacy, Nursing, or equivalent combination of education and experienceExperience in a clinical research organization (CRO) or sponsor environment preferredFamiliarity with GCP, ICH guidelines, and global regulatory standardsStrong project management, organizational, and communication skillsComfortable working independently and embracing new technologiesWillingness to travel up to 25% as neededWhy Join Us:Meaningful Work: Your contributions will directly support critical biomarker research that shapes the future of clinical development and precision medicine.Global Impact: You'll be working on high-profile studies that span multiple regions, making a real difference in patients' lives around the world.Dedicated Team: Join a collaborative, sponsor-dedicated environment where your expertise is trusted, and your voice matters.Flexibility: Enjoy the freedom of a fully remote role with the support of a structured, responsive team.Professional Growth: Be part of a company that invests in your career through continued learning, mentorship, and leadership opportunities.Stability and Vision: Work with a leading global organization known for operational excellence and long-term partnerships in clinical research.If you're passionate about clinical research and want to make a direct impact on advancing biomarker science, we'd love to hear from you.Apply now and be part of a team shaping the future of clinical development.At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time.Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.Salary Range:The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role. Get to know Syneos HealthOver the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. Additional InformationTasks, duties, and responsibilities as listed in this job description are not exhaustive.The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description.The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above.Further, nothing contained herein should be construed to create an employment contract.Occasionally, required skills/experiences for jobs are expressed in brief terms.Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.Summary Roles within Clinical Project Management job family at the M23 level are responsible for planning, directing, creating, and communicating clinical study timelines. These roles gather input from cross-functional teams to create plans that help the team produce deliverables on schedule. They ensure consistency of clinical study and processes across clinical trials, overseeing and resolving operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP), and specific country regulations. Responsibilities include site and vendor selection, preparing clinical trial budgets, and ensuring studies are conducted within clinical trial protocols. These roles also involve monitoring progress and following up with team members and line managers when issues develop. Additionally, they implement and prepare the clinical development strategy as outlined by the clinical teams and may develop trial recruitment strategies. Impact and Contribution Roles within Clinical Project Management job family at the M23 level significantly impact the success of clinical trials by ensuring that all aspects of the study are conducted efficiently and effectively. By gathering input from cross-functional teams and creating detailed plans, these roles help ensure that deliverables are produced on schedule, contributing to the overall success of the clinical trials. Their oversight of operational aspects of clinical trials ensures consistency and adherence to SOP, GCP, and country regulations, which is crucial for the integrity and reliability of the study results. Additionally, their involvement in site and vendor selection, budget preparation, and monitoring progress helps maintain the smooth operation of clinical trials, ultimately contributing to the advancement of clinical research and development. Core Focus •Planning, directing, creating, and communicating clinical study timelines •Overseeing operational aspects of clinical trials •Ensuring consistency across clinical studies •Adhering to SOP, GCP, and country regulations •Selecting sites and vendors •Preparing clinical trial budgets •Monitoring progress and following up with team members and line managers •Implementing and preparing the clinical development strategy •Developing trial recruitment strategies

Federal Work Study Student Job Announcement

Position: Federal Work Study – Student Support Center

Location: Athens Campus

Department: Financial Aid

Reports to: Shirley Moon Financial Aid Coordinator

Salary/Benefits: 10.00 per hour. Maximum 19.5 hour week. No State of Georgia benefits.

Deadline to Apply: August 1, 2025

Responsibilities

Assist marketing program. Operate various office machines including shredders, copiers, keep printers stocked. Filing and maintaining filing. Data entry. Prepare handouts for class.

General and moderately complex clerical and administrative work including basic computer work using Microsoft Office software and internet research. Other clerical duties as assigned, complete errands on campus as needed.

Minimum Qualifications: Current student at Athens Technical College. Must maintain registration of minimum 6 credit hours each semester.

Preferred Qualifications:

· Enrolled student in eligible program of study- registered for minimum 6 credit hours.

· · Complete financial aid file verified by Office of Financial Aid.

· Strong communication skills and work ethic.

·

Interested candidates should apply online at:

To apply, click "Apply to This Job" and submit your cover letter, resume/vita, three (3) professional references, and unofficial transcripts. Incomplete applications will not be considered.

NOTE: Official transcripts will be required upon an offer of employment. Official copies of transcripts may be sent directly to: Athens Technical College, Attn: Human Resources, 800 U.S. Highway 29 N, Athens, GA 30601 or send electronically to .

**Employment is contingent based upon successful completion of appropriate background checks.

Equal opportunity and decisions based on merit are fundamental values of the Technical College System of Georgia (TCSG). The TCSG State Board prohibits discrimination on the basis of an individual’s age, color, disability, genetic information, national origin, race, religion, sex, or veteran status (“protected status”). No individual shall be excluded from participation in, denied the benefits of, or otherwise subjected to unlawful discrimination, harassment, or retaliation under, any TCSG program or activity because of the individual’s protected status; nor shall any individual be given preferential treatment because of the individual’s protected status, except the preferential treatment may be given on the basis of veteran status when appropriate under federal or state law.

Athens Technical College is an equal opportunity employer. All employment processes and decisions, including but not limited to hiring, promotion, and tenure shall be free of ideological tests, affirmations, and oaths, including diversity statements. The basis and determining factor for such decisions should be that the individual possesses the requisite knowledge, skills, and abilities associated with the role, and is believed to have the ability to successfully perform the essential functions, responsibilities, and duties associated with the position for which the person is being considered. At the core of any such decision is ensuring the institution’s ability to achieve its mission and strategic priorities in support of student success.

The following individuals have been designated to coordinate the college's implementation of nondiscrimination policies: Susan Fyffe, Director of Student Support Services, Section 504 and the Americans with Disabilities Act (ADA) Coordinator, Office K-614A, 706/355- 5081, ; Courtney Mattox, Director of Human Resources; Title VI, Title VII, Title IX Coordinator (Employees), Office K-514, , 706/583-2818; and Lenzy Reid, Vice President of Student Affairs, Title IX (Students) Office H-774, 706/355-5029, , 800 U.S. Highway 29 North, Athens, GA 30601.

Join to apply for the Project Integrator (Data Management) role at Omnibus Technologies & Solutions .

Omnibus Technologies & Solutions, LLC is a consulting company that prioritizes stellar customer service. We aim to hire innovative, dedicated, and intelligent talent capable of assisting customers in achieving their organizational goals.

Description

We are hiring a Project Integrator focused on data management. This role supports establishing and improving data management services, including optimizing data compliance, protection, and sharing. The Project Integrator acts as a liaison between the Sponsors and partners teams to ensure accurate information flow. Experience working with NARA is highly desired.

Focus Will Include

• Overseeing the development of ADLS iServices for records management compliance.
• Coordinating core RM programs with dispersed, matrixed teams, including MRI, IMA, and communication efforts.

Required Qualifications:

• Bachelors Degree or 3 years of relevant experience in Management of Information Systems, Computer Science, Engineering, Business, or related field; or 4 years recent IT Project Management or RIM experience, with at least 1 year specific to the skill.
• Experience with federal records management, regulations, policies, and supporting senior leaders.
• Experience drafting records schedules and guidance documentation.
• Ability to work with technical teams on database updates.
• Knowledge of project management methodologies and strong critical thinking skills.
• Proficiency with Microsoft Project, SharePoint, and Office applications.
• Skills in analyzing business and technical data, and translating strategic initiatives into functional requirements.
• Experience coordinating project schedules, meetings, and documentation.

Benefits:

• Comprehensive healthcare coverage including medical, dental, and vision.
• Paid Time Off of 240 hours annually.
• Company-paid life insurance, disability insurance, and supplemental insurances.
• 401(k) retirement plan with 5% company contribution.
• Referral bonus of $5,000 for successful candidate referrals.

Additional Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Engineering and IT
• Industries: IT Services and Consulting

Referrals can double your chances of interview success. Notifications are available for new Project Integrator roles in Herndon, VA.

This job posting is active; no indication of expiration is present.