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Clinical Project Manager Jobs (NOW HIRING)

Collabera

Clinical Project Manager

Santa Clara, CA

Skills 1) Project Management 2) Business Analysis 3) Business Process Modeling 4) Clinical Technology Strategy 5) User Adoption 6) System Training 7) Vendor Management Systems Experience 1) RAVE EDC ...

Bioclinica

Clinical Project Manager

Franklin, TN · On-site

We serve more than 400 pharmaceutical, biotechnology, and device organizations The Clinical Project Manager will focus on study start up through close out activities and perform project analysis ...

Bioclinica

Clinical Project Manager

Princeton, NJ · On-site

We serve more than 400 pharmaceutical, biotechnology, and device organizations The Clinical Project Manager will focus on study start up through close out activities and perform project analysis ...

Collabera

Clinical Project Manager

North Chicago, IL

... Clinical Teams, and Public Affairs). Applies knowledge across multiple therapeutic areas to support ... Appropriately advises management of project risks and presents recommendations for resolution.

SAON LLC

Clinical Project Manager

Pleasant Grove, UT · On-site

We are seeking a Clinical Project Manager to lead the operational execution of clinical studies from study start-up through closeout while ensuring the highest standards of quality, compliance, and ...

Ipsen

Clinical Project Manager

Cambridge, MA

Clinical Project Manager Company: Ipsen Biopharmaceuticals Inc. About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas:

Syneoshealth

CLINICAL PROJECT MANAGER II - ONCOLOGY

OR · Remote

CLINICAL PROJECT MANAGER II - ONCOLOGY Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical ...

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How much do clinical project manager jobs pay per hour?

As of Jun 25, 2026, the average hourly pay for clinical project manager in the United States is $60.70, according to ZipRecruiter salary data. Most workers in this role earn between $42.31 and $71.15 per hour, depending on experience, location, and employer.

What is the movie clinical about?

There is no widely known movie titled 'Clinical.' If referring to a film with a similar name, it may involve themes related to medical or psychological settings. As a Clinical Project Manager, understanding media related to healthcare can help in patient engagement and communication strategies, but the role primarily focuses on managing clinical trials and ensuring regulatory compliance.

What is the difference between Clinical Project Manager vs Clinical Research Associate?

AspectClinical Project ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, with many holding advanced degrees or certifications like PMPUsually holds a Bachelor's degree in life sciences or related field; certifications like CRA certification are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates with sponsors and sitesMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageFound in pharmaceutical, biotech, and CRO companies overseeing entire projectsPrimarily employed by CROs and sponsors to monitor trial sites

The Clinical Project Manager and Clinical Research Associate roles are closely related but differ mainly in scope. The Clinical Project Manager oversees entire clinical trials, manages teams, and coordinates with stakeholders, while the Clinical Research Associate focuses on monitoring clinical sites and ensuring protocol adherence. Both roles require similar educational backgrounds and certifications, but their responsibilities and work environments differ significantly.

What Does a Clinical Project Manager Do?

A clinical project manager, or CPM, manages clinical trial studies for new drugs and medical devices. In this clinical management position, responsibilities and duties include working with all team members and all aspects of a clinical project, including subject selection and enrollment, record keeping, process auditing, and documentation. They also work with the budget and communicate with third parties, such as laboratories or investigators.

What are the key skills and qualifications needed to thrive as a Clinical Project Manager, and why are they important?

To thrive as a Clinical Project Manager, you need expertise in clinical trial management, regulatory compliance, and a relevant life sciences degree, often supported by experience in clinical research. Familiarity with project management tools, electronic data capture (EDC) systems, and certifications like PMP or ACRP are highly valued. Strong leadership, problem-solving, and communication skills help you effectively coordinate teams and stakeholders. These competencies ensure successful trial execution, regulatory adherence, and timely project delivery in a highly regulated environment.

What does it mean for someone to be clinical?

In the context of a Clinical Project Manager, being clinical relates to working within the healthcare or medical research field, often overseeing clinical trials or studies involving patient data and medical interventions. It requires understanding clinical protocols, regulatory requirements, and collaborating with healthcare professionals. Strong organizational skills and knowledge of Good Clinical Practice (GCP) are essential for success in this role.

What is a clinical job?

A clinical job involves working directly with patients or in healthcare settings to support diagnosis, treatment, or research. Roles such as Clinical Project Managers oversee clinical trials, coordinate teams, ensure compliance with regulations, and manage project timelines using tools like electronic data capture systems. These positions often require relevant certifications and a strong understanding of medical protocols.

What does a Clinical Project Manager do?

A Clinical Project Manager oversees the planning, execution, and completion of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They coordinate teams, manage budgets, timelines, and ensure that studies comply with regulatory standards and company protocols. Clinical Project Managers act as the main point of contact between sponsors, vendors, and clinical research sites, working to ensure that trials progress smoothly and data integrity is maintained. Their role is critical in bringing new therapies and treatments to market safely and efficiently.

What are some common challenges Clinical Project Managers face when coordinating multi-site clinical trials?

Clinical Project Managers often encounter challenges such as maintaining consistent communication across different sites, ensuring adherence to regulatory guidelines, and managing timelines amidst unexpected delays. Coordinating multi-site trials requires balancing the needs of diverse teams, addressing site-specific issues, and ensuring data quality across all locations. Effective project management tools, regular status meetings, and proactive risk assessment are essential for overcoming these obstacles and keeping the study on track.

What do we mean by clinical?

In the context of a Clinical Project Manager, 'clinical' refers to activities related to the development, testing, and approval of medical treatments, drugs, or devices. It involves overseeing clinical trials, ensuring compliance with regulatory standards, and managing study teams to gather safety and efficacy data.
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Clinical Project Manager jobs near you
Associate Clinical Project Manager

Associate Clinical Project Manager

Becton, Dickinson and Company

Tempe, AZ • On-site

Full-time

Posted 8 days ago

BD rating

7.2

Company rating: 7.2 out of 10

Based on 136 frontline employees who took The Breakroom Quiz

269th of 419 rated machine equipment manufacturers

Job description

We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
Job Responsibilities: (Primary Duties, Roles, and/or Authorities)
Under direct manager supervision, the Associate Clinical Project Manager will:
  • Manage the quality and compliance of assigned clinical project(s) ensuring that they meet the highest standards for scientific quality, integrity and ethics and are conducted in accordance with BD global clinical procedures, study protocols, GCP and all applicable regulations.

  • Plan and strategize with other business unit cross functional team members (R&D, Marketing, Quality, and other business partners) to define, implement and execute clinical strategies in support of business objectives.

  • Demonstrate a comprehensive understanding of the therapeutic areas and competitive landscapes for assigned clinical project(s).

  • Oversee the planning and execution of assigned clinical projects to ensure that deliverables are completed on time and within budget. Develop and manage metric reporting tools as needed to track project timelines and deliverables. Provide regular and ad hoc reporting of metrics to Clinical Affairs leadership.

  • Manage activities related to clinical strategy and study design, global applications, submissions, and product launches for assigned clinical project(s) as the clinical subject matter expert.

  • Develop Clinical Investigation Plans (CIPs), Informed Consent Forms (ICFs), Investigator's Brochure's (IBs), Clinical Study Management Plans, Study Process Risk Assessments, Regulatory Management Plans, Case Report Forms (CRFs), Clinical Product Management Plans, Clinical Investigation Reports (CIRs) and other essential clinical study documents.

  • Review and provide input on the development of other essential clinical study documents related to clinical data management, clinical statistics, site management & monitoring, clinical safety management, clinical product management and clinical supplier management.

  • Develop and manage clinical study budgets and monthly financial reviews, including invoice review/approval and accruals for assigned clinical project(s).

  • Manage compliance for required reporting, including but not limited to IDE annual reports, clinicaltrials.gov, and overseas notified bodies/competent authorities.

  • Perform study and/or site-level audits of the Trial Master File (TMF) to ensure that study files are current, accurate, complete and audit-ready.

  • Oversee study and site-level management of the Clinical Trial Management System (CTMS) to ensure that study and site details are current, accurate and complete.

  • Interact with and/or oversee interactions with investigational sites, vendors, key opinion leaders (KOLs) and consultants.

  • Manage external contractors/suppliers for assigned clinical project(s) to ensure that deliverables are completed on-time, within budget, and are consistent with the scope of work.

  • Coach and ensure successful and effective relationships between study teams and investigational site personnel.

  • Provide critical thinking and leadership support for issue escalation related to clinical study activities. Interact with investigational sites, vendors, and other functional areas for issues, as needed. Proactively identify issues and create mitigation strategies in collaboration with Clinical Affairs leadership.

  • Provide support for internal or external audits/inspections and ensure resolution of audit/inspection findings related to assigned clinical projects.

  • Conduct Site Management & Monitoring, Clinical Product Management and Clinical Field support activities/visits, as needed.

  • Conduct, attend, or support training and observational activities, as needed, for study team members.

Education and Experience:
  • Bachelor's Degree (BS/BA) in life sciences (MA/MS preferred)

  • 3+ years of experience in clinical research (medical device, pharmaceutical and/or biotechnology)

Knowledge and Skills:
Required Qualifications:
  • Knowledge of domestic and international clinical research regulations and guidelines, Good Clinical Practice (GCP) and current industry practices related to the conduct of clinical studies

  • Proficiency with Microsoft Suite tools (Outlook, Word, Excel, PowerPoint, OneNote, To-Do, SharePoint, etc.)

  • Strong knowledge of clinical study processes and systems (eTMF, CTMS and CDMS)

  • Strong interpersonal and communication (oral and written) skills

  • Strong organizational skills, attention to detail, critical thinking and analytical skills

  • Able to manage and delegate multiple tasks and prioritize importance of tasks/projects

  • Ability to understand and interpret technical, scientific, and clinical information as it applies to product approval activities

  • Ability to lead teams to translate issues into actions, make decisions and influence outcomes

  • Ability to travel up to 40% (or more during peak times)

Preferred Qualifications:
  • Prior experience with clinical studies related to peripheral vascular diseases, end-stage kidney disease and/or oncology

  • Prior experience managing clinical projects (strongly preferred)

  • Experience with medical device studies (strongly preferred)

  • Prior experience with site management & monitoring

  • Prior experience with Veeva Vault Clinical Suite (CTMS, CDMS and eTMF)

  • Professional certification through one or more relevant associations (e.g., ACRP, SOCRA, etc.)

Physical Demands: (if applicable)
While performing the duties of this job, the employee is regularly required to stand, walk, sit, use sight, and use hands to manipulate, handle or feel objects, tools, controls, and office equipment. The employee frequently is required to verbally communicate with other associates. The employee is occasionally required to reach with hands and arms and stoop, kneel or crouch.
Work Environment: (if applicable)
While performing the duties of this job, the employee may be in an open cubicle environment. Candidate must be able to work in a team-oriented, fast-paced environment. BD is an affirmative action, equal opportunity employer that values and actively seeks diversity in the workforce.
Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visit https://bd.com/careers.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Required Skills
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Primary Work Location
USA AZ - Tempe Headquarters
Additional Locations
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About BD

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BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

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Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

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