38,408 Lead Programmer jobs in the United States

Company Overview:
Req ID:
NTT DATA strives to hire exceptional, innovative and passionate individuals who want to grow with us. If you want to be part of an inclusive, adaptable, and forward-thinking organization, apply now.
We are currently seeking a Lead Systems Programmer to join our team in Alpharetta, Georgia (US-GA), United States (US).
Job Description:
Responsibilities
Design, implement, and maintain Windows Server environments with a focus on performance, reliability, and scalability.
Develop and maintain PowerShell scripts for automation of administrative tasks and system monitoring.
Manage and optimize SQL and DB2 database environments, including stored procedures and performance tuning.
Collaborate with cross-functional teams including architects, developers, and business stakeholders to ensure infrastructure solutions align with business needs.
Participate in system design reviews, testing workshops, and technical planning sessions.
Lead efforts in identifying and resolving infrastructure defects and performance issues.
Drive continuous improvement initiatives focused on operational excellence and process optimization.
Mentor junior engineers and contribute to knowledge sharing across the team.
Mandatory Skills
6+ Years of proficiency in PowerShell scripting and automation.
5+ Years of strong experience with SQL and DB2 database environments.
4+Years of Deep understanding of Windows Server architecture and administration.
3+ Years of exposure to .NET technologies (preferred but not required).
Ideal Mindset:
Lifelong Learner: You are always seeking to improve your technical and nontechnical skills.
Team Player: You are someone who wants to see everyone on the team succeed and is willing to go the extra mile to help a teammate in need.
Communicator: You know how to communicate your design ideas to both technical and nontechnical stakeholders, prioritizing critical information and leaving out extraneous details.
Must reside in the US
Where required by law, NTT DATA provides a reasonable range of compensation for specific roles. The starting pay range for this remote role is ***-*** This range reflects the minimum and maximum target compensation for the position across all US locations. Actual compensation will depend on a number of factors, including the candidate s actual work location, relevant experience, technical skills, and other qualifications.
This position is eligible for company benefits including medical, dental, and vision insurance with an employer contribution, flexible spending or health savings account, life and AD&D insurance, short and long term disability coverage, paid time off, employee assistance, participation in a 401k program with company match, and additional voluntary or legally-required benefits.
*This position is not open to employer sponsorship**
#Launchjobs #LaunchEngineering
About NTT DATA:
NTT DATA is a $30 billion trusted global innovator of business and technology services. We serve 75% of the Fortune Global 100 and are committed to helping clients innovate, optimize and transform for long term success. As a Global Top Employer, we have diverse experts in more than 50 countries and a robust partner ecosystem of established and start-up companies. Our services include business and technology consulting, data and artificial intelligence, industry solutions, as well as the development, implementation and management of applications, infrastructure and connectivity. We are one of the leading providers of digital and AI infrastructure in the world. NTT DATA is a part of NTT Group, which invests over $3.6 billion each year in R&D to help organizations and society move confidently and sustainably into the digital future. Visit us at us.nttdata.com
NTT DATA endeavors to make accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact us at This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. NTT DATA is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. For our EEO Policy Statement, please click here. If you d like more information on your EEO rights under the law, please click here. For Pay Transparency information, please click here.

**Job Description Summary**
Are you passionate about innovation? Are you excited at the opportunity to electrify and decarbonize the world?
We operate with a founder's mindset. We deliver innovation with passion, speed, and courage. We continuously challenge our thinking and are empowered to dream big and take smart risks.
As a member of the CAD/CAM team, you will be an active contributor to the factory volume ramp and standardization efforts.
**Job Description**
**What you'll do**
+ Generate and maintain CNC programs utilizing NX-CAM or other software. This could include multi-axis milling, turning, grinding and/or EDM.
+ Verify new CNC programs prior to release on the shop floor utilizing Vericut.
+ Provide CNC related support to M.E. (Manufacturing Engineer) and provide operator training during new / rebuilt machine startup and / or process improvements.
+ Provide daily operator support in the form of CNC programming and troubleshooting support to the shop floor.
+ Support and implement tooling & fixturing requirements associated with CNC machine tools.
+ Generate and support workstation instructions (methods) for CNC related issues.
+ Initiate and lead process improvement projects to improve safety, quality, cost and delivery.
+ Provide effective communication to appropriate team members when needed.
+ Work effectively as an individual and in a team-based environment in a matrixed organization.
+ Work effectively in a fast-paced environment while embracing and driving positive change inside and outside the organization when appropriate.
**What you'll bring (Basic Qualifications)**
+ Bachelor's Degree, Associate's Degree, or Machinist Apprentice (or similar) graduate with 3 years of experience with graphical based CAM System CNC Programming (OR) High School Degree w/6 years of experience with graphical based CAM System CNC Programming.
+ 3+ years experience NX CAM Programming
**What will make you stand out**
+ Experience creating 5-axis CNC programs using a CAM (preferably NX) system.
+ Minimum of 1 year of experience with high-level machine tool controls including sub-routine(macro), Renishaw probing routine, and variable based programming, as well as CLM (closed loop machining)
+ Bachelor degree in Engineering or Machine Tool Technology.
+ Strong problem solving and organization skills, with above average shop math skills in geometry and trigonometry.
+ Knowledge of post-processor development and debugging, preferably NX Post Configurator.
+ Experience using Vericut (preferred) or other CNC verification/machine simulation software.
+ Strong familiarity with multiple machine controls including Fanuc, Haas, Okuma, Siemens, and G&L
+ Demonstrated proficiency interpreting drawing requirements.
+ Experience with large precision grinding applications
+ Ability to multi-task and productively manage multiple projects concurrently.
+ Experience machining high temperature superalloys found in HDGT or Aerospace components.
The salary range for this position is $81,700.00 - 109,200.00 USD annually. The specific pay offered may be influenced by a variety of factors, including the candidate's experience, education, and skill set. This position is also eligible for bonuses, such as a performance bonus/variable incentive compensation/equity.
Healthcare benefits include medical, dental, vision, and prescription drug coverage; access to a Health Coach, a 24/7 nurse-based resource; and access to the Employee Assistance Program, providing 24/7 confidential assessment, counseling, and referral services. Retirement benefits include the GE Retirement Savings Plan, a tax-advantaged 401 (k) savings opportunity with company matching contributions and company retirement contributions, as well as access to Fidelity resources and planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability insurance, life insurance, and paid time-off for vacation or illness.
General Electric Company, Ropcor, Inc., and in some cases their affiliates, each sponsor certain employee benefit plans or programs (i.e., is a "Sponsor"). Each Sponsor reserves the right to terminate, amend, suspend, replace, or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a Sponsor's welfare benefit plan or program. This document does not create a contract of employment with any individual.
_This role requires access to U.S. export-controlled information. If applicable, final offers will be contingent on ability to obtain authorization for access to U.S. export-controlled information from the U.S. Government._
**Additional Information**
GE Vernova offers a great work environment, professional development, challenging careers, and competitive compensation. GE Vernova is an Equal Opportunity Employer ( . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE Vernova will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
**Relocation Assistance Provided:** Yes
GE Vernova is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

**Job Description Summary**
The Lead CMM Programmer will play a key role in programming and optimizing Coordinate Measuring Machines (CMMs) to support the manufacturing of Combustion & Structural Components. The Lead CMM programmer will utilize PC-DMIS software and Hexagon CMMs, with additional work involving other software tools. This role encompasses writing, editing, troubleshooting, validating, and improving CMM programs to ensure precise measurement of aerospace components. The Lead CMM Programmer will collaborate closely with Operations, Quality Engineering, and Machining Process Engineering to meet compliance standards and production requirements. They will also communicate inspection methodologies and oversee process monitoring in alignment with production schedules. Proficiency in reading and interpreting drawings and prints using Geometric Dimensioning and Tolerancing (GD&T) principles is essential.
**Job Description**
**Roles and Responsibilities**
+ Develop and optimize CMM programs using PC-DMIS and other software, leveraging both CAD models and prints.
+ Lead and manage the implementation of inspection processes for new products and design changes, from fixture procurement to production-ready program rollout.
+ Interpret and apply advanced GD&T principles to ensure dimensional accuracy and compliance.
+ Create planning documents, processes, and work instructions while providing proactive support to meet manufacturing needs around the flow of CMM inspection.
+ Troubleshoot and validate CMM/PC-DMIS programs, conduct GR&R studies, and verify results using multiple techniques.
+ Adhere to system standards for development, implementation, and change management of metrology processes.
+ Work independently and collaboratively to identify needs and develop validation plans.
+ Coordinate with cross-functional teams to ensure programming milestones align with project timelines.
+ Provide technical mentorship and guidance to other engineers and operators within the department.
**Required Qualifications**
+ Bachelor's Degree from an accredited college or university (or a high school diploma/GED with a minimum of 4 years manufacturing experience) + minimum of 3 years CMM Programming experience
**Desired Characteristics**
+ Strong oral and written communication skills. Demonstrated ability to analyze and resolve problems. Ability to document, plan, market, and execute programs. Established project management skills.
+ Developed knowledge/experience programming CMM's using PCDMIS software with an emphasis on precision, repeatability and reproducibility.
+ Advanced knowledge of GD&T and its application in inspection routines to meet print specifications.
+ Strong mathematical, analytical, writing, and communication skills.
+ Knowledge and experience with CAD-based inspection using PC-DMIS.
+ Strong collaboration and presentation skills to effectively communicate program/process implementation.
+ Knowledge and experience with manual gages to troubleshoot and validate CMM data.
+ Previous high-volume manufacturing shop experience in Metrology / Inspection discipline
GE Aerospace offers comprehensive benefits and programs to support your health and, along with programs like HealthAhead, your physical, emotional, financial and social wellbeing. Healthcare benefits include medical, dental, vision, and prescription drug coverage; access to a Health Coach from GE Aerospace; and the Employee Assistance Program, which provides 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Aerospace Retirement Savings Plan, a 401(k) savings plan with company matching contributions and company retirement contributions, as well as access to Fidelity resources and planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability insurance, life insurance, and paid time-off for vacation or illness.
GE Aerospace (General Electric Company or the Company) and its affiliates each sponsor certain employee benefit plans or programs (i.e., is a "Sponsor"). Each Sponsor reserves the right to terminate, amend, suspend, replace or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a Sponsor's welfare benefit plan or program. This document does not create a contract of employment with any individual.
_This role requires access to U.S. export-controlled information. Therefore, employment will be contingent upon the ability to prove that you meet the status of a U.S. Person as one of the following: U.S. lawful permanent resident, U.S. Citizen, have been granted asylee or refugee status (i.e., a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3))._
**Additional Information**
GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer ( . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
**Relocation Assistance Provided:** Yes
GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

**Job Description Summary**
The Lead CMM programmer will demonstrate leadership in supporting the plant CMM measurement needs including Program revision control. In the Lead CMM programmer role, you will utilize your experience and expertise to solve CMM problems, develop and execute program objectives, and manage CMM program schedules.
**Job Description**
**Roles and Responsibilities**
+ Develop and validate Coordinate Measuring Machines (CMM) programs and calibrations used to support the manufacturing efforts for GE Aviation Wilmington
+ Plan and specify CMM purchases necessary to inspect drawing and specification requirements
+ Plan and coordinate the activities of the entire CMM staff by managing CMM calibration responsibilities as assigned including: CMM programming / calibration; Measurement Audit Support; CMM Program revision control
+ Plan and coordinate the CMM area activities around Program Schedules, Calibration, Audit Support and Program Software Quality Assurance controls
+ Responsible for the measurement accuracy of all CMM measurement systems
+ Conduct training CMM inspection and programming as needed
+ Act as plant expert and interface regarding CMM measurements
+ Ensure a means of collecting and distributing compiled information in order to improve quality
+ Responsible for the administration of the plant CMM's, including implementation and maintenance to regulatory requirements and standards such as applicable ISO standards
+ Read and interpret drawings and other quality control requirements using Geometric Dimensioning and Tolerancing (GD&T) and sound metrology principals
+ Ensure safe practices are used in compliance with all governmental regulations
+ Work with Quality team to drive inspection process improvements
+ Drive Lean effort within manufacturing focusing on Quality
**Required Qualifications**
+ Bachelor's degree from an accredited university or college (Or a high school diploma / GED with a minimum of 4 years of experience in engineering or quality) + 3 years CMM programming experience including MODUS and PCDMIS and PolyWorks (including experience with editing and controlling CMM program revisions) for aviation hardware
**Desired Characteristics**
+ PolyWorks, PCDMIS, and/or Modus programming language experience.
+ Strong organizational, analytic, and problem- solving skills
+ Ability to work in cross- functional teams in a matrix environment with all levels of personnel
+ Strong working knowledge of Manufacturing and Quality operations
+ Ability to plan, prioritize, and manage multiple priorities under tight deadlines
+ Ability to coach, manage, change and facilitate team performance
+ Ability to analyze problems, identify root causes and provide efficient solutions
+ Ability to drive change
+ Demonstrated oral and written communication skills
+ Strong interpersonal and leadership skills
+ Six Sigma training
+ Humble: respectful, receptive, agile, eager to learn
+ Transparent: shares critical information, speaks with candor, contributes constructively
+ Focused: quick learner, strategically prioritizes work, committed
+ Leadership ability: strong communicator, decision-maker, collaborative
+ Problem solver: analytical-minded, challenges existing processes, critical thinker
GE Aerospace offers comprehensive benefits and programs to support your health and, along with programs like HealthAhead, your physical, emotional, financial and social wellbeing. Healthcare benefits include medical, dental, vision, and prescription drug coverage; access to a Health Coach from GE Aerospace; and the Employee Assistance Program, which provides 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Aerospace Retirement Savings Plan, a 401(k) savings plan with company matching contributions and company retirement contributions, as well as access to Fidelity resources and planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability insurance, life insurance, and paid time-off for vacation or illness.
GE Aerospace (General Electric Company or the Company) and its affiliates each sponsor certain employee benefit plans or programs (i.e., is a "Sponsor"). Each Sponsor reserves the right to terminate, amend, suspend, replace or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a Sponsor's welfare benefit plan or program. This document does not create a contract of employment with any individual.
_This role requires access to U.S. export-controlled information. Therefore, for applicants who are not U.S. lawful permanent residents, U.S. Citizens, or have been granted asylee or refugee status (i.e., not a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3), otherwise known as a U.S. Person), employment will be contingent on the ability to obtain authorization for access to U.S. export-controlled information from the U.S. Government._
**Additional Information**
GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer ( . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
**Relocation Assistance Provided:** Yes
GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Our client is searching for a passionate and experienced Lead Film Programmer to curate and manage their film programming initiatives in Jacksonville, Florida, US . This pivotal role involves developing a diverse and engaging film lineup for various venues and events, identifying emerging trends, and fostering relationships within the film community. You will be instrumental in shaping the cinematic experience for audiences, from blockbuster premieres to independent art-house features.

Responsibilities include:

• Developing and implementing a comprehensive film programming strategy aligned with organizational goals and audience interests.
• Researching, identifying, and securing rights for a wide range of films, including features, documentaries, shorts, and international cinema.
• Curating film series, festivals, and special events, ensuring thematic coherence and audience appeal.
• Building and maintaining strong relationships with distributors, filmmakers, and industry professionals.
• Collaborating with marketing and communications teams to promote film programming effectively.
• Overseeing the technical aspects of film projection and presentation, ensuring high-quality screenings.
• Managing the programming budget and negotiating licensing agreements.
• Providing insightful commentary and context for selected films through written materials or live introductions.
• Staying abreast of current trends and innovations in the film industry and exhibition landscape.
• Supervising and mentoring assistant programmers and volunteers.
• Analyzing audience feedback and attendance data to refine programming choices.

The successful candidate will have a Bachelor's degree in Film Studies, Cinema, or a related field, with at least 5 years of experience in film programming, curation, or exhibition. A deep knowledge of film history, genres, and contemporary cinema is essential. Exceptional organizational, negotiation, and interpersonal skills are required. The ability to work independently and as part of a collaborative team, coupled with a keen eye for compelling cinematic content, will make you an ideal fit for this exciting opportunity.

Our client, a renowned cultural institution in Philadelphia, Pennsylvania , is seeking an experienced and visionary Lead Film Programmer to curate and manage its diverse film exhibition program. This is an exceptional opportunity for a passionate film aficionado to shape the cinematic experience for a vibrant audience. The Lead Film Programmer will be responsible for developing and implementing a comprehensive film screening schedule across various genres, including independent, documentary, international, and classic cinema. This includes identifying and securing film rights, negotiating exhibition terms with distributors, and building strong relationships within the global film community.

You will oversee all aspects of film programming, from conceptualization to execution, ensuring a high-quality and engaging offering that aligns with the institution's mission and artistic vision. This involves staying abreast of current trends in filmmaking, emerging directors, and significant cinematic anniversaries. The role requires developing innovative thematic programs, film series, and festival collaborations. You will also play a key role in marketing and audience development, working closely with the communications team to promote film events and drive attendance. Responsibilities include managing the film program budget, tracking expenditures, and reporting on program success metrics. Directing and mentoring junior programming staff and volunteers will also be a significant part of your role. The ideal candidate will have a proven track record of successful film curation and a deep understanding of film history and theory.

The Lead Film Programmer will need a Bachelor's degree in Film Studies, Cinema, or a related humanities field; a Master's degree is preferred. A minimum of 7 years of progressive experience in film programming, curating, or festival management is required. Demonstrated experience in film acquisition, rights negotiation, and distribution landscape is essential. Exceptional knowledge of film history, genres, and international cinema is paramount. Excellent organizational, communication, and interpersonal skills are necessary to effectively collaborate with internal teams, external partners, and the public in Philadelphia, Pennsylvania . A passion for engaging diverse audiences with impactful cinematic storytelling is a must.

**PXL is seeking a clinical operations lead with expertise in clinical sample logistics and proficiency in computational programming to support the generation and delivery of quality biomarker samples and data.**
Responsibilities will include one or more of the following: development of tools and dashboards for sample/data tracking, review of clinical sample collection, resolving sample/data queries, and support of database lock (DBL) activities. Proficiency in Python, R, MATLAB, and/or SQL programming is required.
The candidate will develop, drive, and handle clinical study related tasks for the team in collaboration with Precision Medicine Companion Diagnostics Operations, Laboratory Managers and Clinical Laboratory Study Management. Expertise in one or more of the following areas is required: samples, kits, data, and logistics operations for clinical trials. Understanding of one or more of the following is preferred: central labs, specialty testing labs, data operations, database development, LIMS, kit inventory management and sample tracking processes.
Job Responsibilities:
- Establish and streamline processes to increase efficiency and implement analytical tools to advance departmental goals.
- Oversee operations, including samples, kits, and data processes, ensuring integrity and completeness for database locks.
- Use technical tools/systems and programming languages to systematically clean data, including processing confidential data according to guidelines.
- Programmatically aggregate and extract key information from operational reports
- Possess knowledge of structured data, such as entities, classes, hierarchies, relationships, and metadata, with the ability to perform data mapping
- Support processing of informed consent forms (ICFs) and ensure compliance with ICFs for internal sample handling, tracking, usage, and destruction.
- Manage sample-related issues with central and specialty labs, acting as the primary point of contact for resolution.
- Maintain and review metrics related to clinical study samples, data, kits, and logistics.
- Lead cross-functional study teams, manage vendor relationships, and oversee clinical trial biosamples and data monitoring.
- Oversee and manage clinical trial biosamples and data monitoring and completeness from collection through to disposal, per requirements of the study
- Anticipate challenges, manage dependencies, and mitigate risks across projects.
- Enhance communication with senior stakeholders and align functions with group objectives.
- Participate in vendor oversight activities, including issue escalation, metrics reviews, and performance monitoring
**Job Requirements:**
- Proficiency in one or more programming languages (R, Python, Perl, SQL, MATLAB)
- Familiarity with APIs, database development, dashboard development, and Linux/Unix environments
- Ability to critically analyze and plan for sample interdependencies, risks, and issues with an awareness of the impacts to clinical studies/program.
- Strong problem-solving, project management, and organizational skills, with ability to effectively multi-task and prioritize.
- Extensive process development and project management experience including vendor management
- Excellent oral and written communication and presentation skills
- Advanced excel knowledge required
- 7+ years of experience in clinical operations preferred.
**Education:**
- Bachelor's or master's degree.
**Experience:**
- 6+ years of clinical research experience in academic, CRO, or pharmaceutical/biotech settings, with knowledge of clinical trials and clinical databases.
#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

**PXL is seeking a clinical operations lead with expertise in clinical sample logistics and proficiency in computational programming to support the generation and delivery of quality biomarker samples and data.**
Responsibilities will include one or more of the following: development of tools and dashboards for sample/data tracking, review of clinical sample collection, resolving sample/data queries, and support of database lock (DBL) activities. Proficiency in Python, R, MATLAB, and/or SQL programming is required.
The candidate will develop, drive, and handle clinical study related tasks for the team in collaboration with Precision Medicine Companion Diagnostics Operations, Laboratory Managers and Clinical Laboratory Study Management. Expertise in one or more of the following areas is required: samples, kits, data, and logistics operations for clinical trials. Understanding of one or more of the following is preferred: central labs, specialty testing labs, data operations, database development, LIMS, kit inventory management and sample tracking processes.
Job Responsibilities:
- Establish and streamline processes to increase efficiency and implement analytical tools to advance departmental goals.
- Oversee operations, including samples, kits, and data processes, ensuring integrity and completeness for database locks.
- Use technical tools/systems and programming languages to systematically clean data, including processing confidential data according to guidelines.
- Programmatically aggregate and extract key information from operational reports
- Possess knowledge of structured data, such as entities, classes, hierarchies, relationships, and metadata, with the ability to perform data mapping
- Support processing of informed consent forms (ICFs) and ensure compliance with ICFs for internal sample handling, tracking, usage, and destruction.
- Manage sample-related issues with central and specialty labs, acting as the primary point of contact for resolution.
- Maintain and review metrics related to clinical study samples, data, kits, and logistics.
- Lead cross-functional study teams, manage vendor relationships, and oversee clinical trial biosamples and data monitoring.
- Oversee and manage clinical trial biosamples and data monitoring and completeness from collection through to disposal, per requirements of the study
- Anticipate challenges, manage dependencies, and mitigate risks across projects.
- Enhance communication with senior stakeholders and align functions with group objectives.
- Participate in vendor oversight activities, including issue escalation, metrics reviews, and performance monitoring
**Job Requirements:**
- Proficiency in one or more programming languages (R, Python, Perl, SQL, MATLAB)
- Familiarity with APIs, database development, dashboard development, and Linux/Unix environments
- Ability to critically analyze and plan for sample interdependencies, risks, and issues with an awareness of the impacts to clinical studies/program.
- Strong problem-solving, project management, and organizational skills, with ability to effectively multi-task and prioritize.
- Extensive process development and project management experience including vendor management
- Excellent oral and written communication and presentation skills
- Advanced excel knowledge required
- 7+ years of experience in clinical operations preferred.
**Education:**
- Bachelor's or master's degree.
**Experience:**
- 6+ years of clinical research experience in academic, CRO, or pharmaceutical/biotech settings, with knowledge of clinical trials and clinical databases.
#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

**PXL is seeking a clinical operations lead with expertise in clinical sample logistics and proficiency in computational programming to support the generation and delivery of quality biomarker samples and data.**
Responsibilities will include one or more of the following: development of tools and dashboards for sample/data tracking, review of clinical sample collection, resolving sample/data queries, and support of database lock (DBL) activities. Proficiency in Python, R, MATLAB, and/or SQL programming is required.
The candidate will develop, drive, and handle clinical study related tasks for the team in collaboration with Precision Medicine Companion Diagnostics Operations, Laboratory Managers and Clinical Laboratory Study Management. Expertise in one or more of the following areas is required: samples, kits, data, and logistics operations for clinical trials. Understanding of one or more of the following is preferred: central labs, specialty testing labs, data operations, database development, LIMS, kit inventory management and sample tracking processes.
Job Responsibilities:
- Establish and streamline processes to increase efficiency and implement analytical tools to advance departmental goals.
- Oversee operations, including samples, kits, and data processes, ensuring integrity and completeness for database locks.
- Use technical tools/systems and programming languages to systematically clean data, including processing confidential data according to guidelines.
- Programmatically aggregate and extract key information from operational reports
- Possess knowledge of structured data, such as entities, classes, hierarchies, relationships, and metadata, with the ability to perform data mapping
- Support processing of informed consent forms (ICFs) and ensure compliance with ICFs for internal sample handling, tracking, usage, and destruction.
- Manage sample-related issues with central and specialty labs, acting as the primary point of contact for resolution.
- Maintain and review metrics related to clinical study samples, data, kits, and logistics.
- Lead cross-functional study teams, manage vendor relationships, and oversee clinical trial biosamples and data monitoring.
- Oversee and manage clinical trial biosamples and data monitoring and completeness from collection through to disposal, per requirements of the study
- Anticipate challenges, manage dependencies, and mitigate risks across projects.
- Enhance communication with senior stakeholders and align functions with group objectives.
- Participate in vendor oversight activities, including issue escalation, metrics reviews, and performance monitoring
**Job Requirements:**
- Proficiency in one or more programming languages (R, Python, Perl, SQL, MATLAB)
- Familiarity with APIs, database development, dashboard development, and Linux/Unix environments
- Ability to critically analyze and plan for sample interdependencies, risks, and issues with an awareness of the impacts to clinical studies/program.
- Strong problem-solving, project management, and organizational skills, with ability to effectively multi-task and prioritize.
- Extensive process development and project management experience including vendor management
- Excellent oral and written communication and presentation skills
- Advanced excel knowledge required
- 7+ years of experience in clinical operations preferred.
**Education:**
- Bachelor's or master's degree.
**Experience:**
- 6+ years of clinical research experience in academic, CRO, or pharmaceutical/biotech settings, with knowledge of clinical trials and clinical databases.
#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.