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Clinical Project Manager

Blue Bell, PA · Remote

Clinical Project Manager, Immunology - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Telix Pharmaceuticals (AMER)

OR

See Yourself at Telix The Clinical Project Manager (CPM) is responsible to support and oversee the day-to-day responsibilities of multiple early phase regional clinical trials from protocol ...

Calyxo, Inc.

Clinical Project Manager

Pleasanton, CA

$140K - $150K/yr

The Clinical Project Manager plays a critical role in leading the execution of clinical trials from start to finish. This position ensures trials are conducted efficiently, on time, and in full ...

Unison Health

Clinical Project Manager

Toledo, OH

The Clinical Project Manager - OhioRISE Program is a management position responsible for planning, coordinating, implementing, and monitoring clinical and operational initiatives within the ...

Unison Health

Clinical Project Manager

Toledo, OH · On-site

The Clinical Project Manager - OhioRISE Program is a management position responsible for planning, coordinating, implementing, and monitoring clinical and operational initiatives within the ...

Crinetics Pharmaceuticals

Clinical Project Manager

$119K - $149K/yr

The Clinical Project Manager (CPM) is responsible for timeline and budget management for assigned clinical studies within Clinical Operations. The CPM serves as a key contributor to study and program ...

IQVIA

Clinical Project Manager

Durham, NC · On-site

Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own ...

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How much do junior clinical project manager jobs pay per year?

As of Jun 13, 2026, the average yearly pay for junior clinical project manager in the United States is $72,482.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,000.00 and $84,000.00 per year, depending on experience, location, and employer.

What are some typical challenges a Junior Clinical Project Manager might face when coordinating multiple clinical trial sites?

As a Junior Clinical Project Manager, one common challenge is ensuring consistent communication and protocol adherence across multiple trial sites, which may be in different locations or time zones. Balancing timelines, managing site-specific issues, and handling varying levels of staff experience require strong organizational and interpersonal skills. Additionally, junior managers often need to quickly learn regulatory requirements and adapt to rapidly changing project priorities, all while supporting senior project managers and cross-functional teams. Proactively seeking feedback and maintaining clear documentation can help overcome these challenges.

What does a Junior Clinical Project Manager do?

A Junior Clinical Project Manager assists in planning, coordinating, and overseeing clinical trials to ensure they are conducted according to regulatory standards and timelines. They support senior project managers by monitoring trial progress, managing documentation, coordinating with research teams, and helping resolve issues that arise during the study. This role often involves communication with sponsors, investigators, and other stakeholders, as well as administrative tasks such as scheduling meetings and tracking project milestones. Junior Clinical Project Managers play a crucial role in ensuring the smooth and efficient execution of clinical research projects.

What is the difference between Junior Clinical Project Manager vs Clinical Trial Coordinator?

AspectJunior Clinical Project ManagerClinical Trial Coordinator
CredentialsBachelor's degree in life sciences; some roles prefer project management certificationBachelor's degree in life sciences or related field
Work EnvironmentManages multiple projects, collaborates with teams, oversees timelinesSupports trial activities, manages documentation, coordinates with sites
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, hospitals, CROs
Common Search & ComparisonOften compared for entry-level project management roles in clinical trialsOften compared as a support role in clinical research

The Junior Clinical Project Manager typically has more responsibilities in managing clinical trial projects and overseeing teams, while the Clinical Trial Coordinator focuses on supporting trial activities and site coordination. Both roles require similar educational backgrounds but differ in scope and level of responsibility within clinical research teams.

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

To thrive as a Junior Clinical Project Manager, you need a background in life sciences or a related field, strong organizational skills, and familiarity with clinical trial processes. Proficiency with clinical trial management systems (CTMS), Microsoft Office, and understanding of GCP guidelines are commonly required, and certifications like PMI or ACRP are advantageous. Attention to detail, effective communication, and the ability to collaborate with cross-functional teams are important soft skills in this role. These skills ensure efficient trial execution, regulatory compliance, and successful coordination among stakeholders in complex clinical environments.
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Junior Clinical Project Manager jobs near you
Infographic showing various Junior Clinical Project Manager job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 66% Full Time, 22% Part Time, and 11% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $72,482 per year, or $34.8 per hour.
Clinical Project Manager

Clinical Project Manager

PharmaOut

Gaithersburg, MD

Other

Posted 25 days ago

Job description

Job Description This role will be key in developing internal Clinical Operations systems and procedures to improve all aspects of Clinical Study related business processes and will work very closely with the Associate Director of Clinical Operations along with the US Site Head. Location: Gaithersburg, Maryland Responsibilities: Participates in the planning, implementation and management of pre-IND through Phase I-II clinical trials, in collaboration with Contract Research Organization (CRO) partners, if applicable. Manage day to day activities of all aspects of clinical studies including study plans, timelines, problem identification and resolution, status reports and budget to ensure timely delivery of completed study reports to the project teams.

Contributes to development of RFPs and participates in selection of CROs/vendors. Manages CRO and vendor activities to ensure adherence to deliverables and timelines. Provides updates on project status and deliverables to Clinical Project Management leads (deliverables may include project status reports, vendor reports, trackers, meeting minutes/action items).

Contributes to development of study budget(s). Maintains primary responsibility for the content of and execution on all study-related operational plans, such as study operations manuals, vendor manuals, safety plans, project management plans, communication plans, and quality plans, whether developed internally or externally. Oversees investigator recruitment/selection and the conduct of trials at investigative sites.

Participate as necessary in monitoring visits (co-monitoring), reviews monitoring visit reports and ensures CRO quality within trials, if applicable. Plans, executes, and leads Investigators Meetings, if applicable. Contributes to development of internal Clinical Operations systems to improve business processes.

Develops relationships with Key Opinion Leaders as applicable for key I-Mab development programs. Prepare and present study or project specific updates. Represent Project Management & Clinical Operations in partnered development programs.

Mentors junior level Clinical Research Associates. Qualifications: Life sciences or medical background is required. 6+ years of industry experience (biotech/pharma) with at least 2-5 (will determine level) years of project management experience Experience in Phase 1 Oncology trials.

Strong understanding of ICH, GCP and relevant regulatory requirements The ability to work with cross-functional teams in a matrix environment is a must Strong organizational and time management skills; detailed oriented; excellent interpersonal and communication skills Proficiency with Microsoft Outlook, Excel, Word, PowerPoint and Project.

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