Clinical Project Manager
Gaithersburg, MD ยท On-site
Mentors junior level Clinical Research Associates. Qualifications: Life sciences or medical ... level) years of project management experience Experience in Phase 1 Oncology trials. Strong ...
Gaithersburg, MD ยท On-site
Mentors junior level Clinical Research Associates. Qualifications: Life sciences or medical ... level) years of project management experience Experience in Phase 1 Oncology trials. Strong ...
Gaithersburg, MD ยท On-site
Mentors junior level Clinical Research Associates. Qualifications: Life sciences or medical ... level) years of project management experience Experience in Phase 1 Oncology trials. Strong ...
Blue Bell, PA ยท On-site
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 ...
Blue Bell, PA ยท On-site
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 ...
San Rafael, CA ยท On-site
Project Manager (Clinical/Biomedical) Location: San Rafael CA - Hybrid (2 days/week onsite) Duration: 6-12 months Mandatory: Recent/Prior Bio/Clinical Domain exp Keywords: * Drug development
San Rafael, CA ยท On-site
Project Manager (Clinical/Biomedical) Location: San Rafael CA - Hybrid (2 days/week onsite) Duration: 6-12 months Mandatory: Recent/Prior Bio/Clinical Domain exp Keywords: * Drug development
Blue Bell, PA ยท 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 ...
Blue Bell, PA ยท 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 ...
Clinical Project Manager Location: Lexington, MA Duration: 6 Months+ (Temp to Perm) Summary: The Clinical Project Manager is responsible for independently managing a small number of studies of basic ...
Clinical Project Manager Location: Lexington, MA Duration: 6 Months+ (Temp to Perm) Summary: The Clinical Project Manager is responsible for independently managing a small number of studies of basic ...
Skaneateles, NY ยท On-site
Clinical Project Manager Location: Skaneateles, NY Duration: 4 Months Summary: Responsible for managing the organization and conduct of clinical studies in compliance with Clinical Operations ...
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Skaneateles, NY ยท On-site
Clinical Project Manager Location: Skaneateles, NY Duration: 4 Months Summary: Responsible for managing the organization and conduct of clinical studies in compliance with Clinical Operations ...
Franklin Lakes, NJ ยท On-site
Clinical Project Manager Location: Franklin Lakes, NJ Duration: 9+ Months Contract Total Hours/week: 40.00 1st Shift Client: Medical Device Company Employment Type: Contract on W2 (Need US Citizens ...
Franklin Lakes, NJ ยท On-site
Clinical Project Manager Location: Franklin Lakes, NJ Duration: 9+ Months Contract Total Hours/week: 40.00 1st Shift Client: Medical Device Company Employment Type: Contract on W2 (Need US Citizens ...
Waltham, MA ยท On-site
$130K - $150K/yr
Help mentor and train junior members of the clinical team in the area of clinical operations as ... Demonstrates strong project management skills * Understanding of ICH and regulatory environment as ...
Waltham, MA ยท On-site
$130K - $150K/yr
Help mentor and train junior members of the clinical team in the area of clinical operations as ... Demonstrates strong project management skills * Understanding of ICH and regulatory environment as ...
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 ...
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 ...
$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 ...
$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 ...
Toledo, OH ยท 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 ...
New
Toledo, OH ยท 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 ...
New
Los Angeles, CA ยท On-site
The Department of Psychiatry and Behavioral Sciences at the University of Southern California is seeking a Clinical Project Manager to support NIH- and foundation-funded clinical research programs ...
Los Angeles, CA ยท On-site
The Department of Psychiatry and Behavioral Sciences at the University of Southern California is seeking a Clinical Project Manager to support NIH- and foundation-funded clinical research programs ...
Los Angeles, CA ยท Hybrid
The Department of Psychiatry and Behavioral Sciences at the University of Southern California is seeking a Clinical Project Manager to support NIH- and foundation-funded clinical research programs ...
Los Angeles, CA ยท Hybrid
The Department of Psychiatry and Behavioral Sciences at the University of Southern California is seeking a Clinical Project Manager to support NIH- and foundation-funded clinical research programs ...
Toledo, OH ยท 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 ...
New
Toledo, OH ยท 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 ...
New
$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 ...
$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 ...
Los Angeles, CA ยท Hybrid
The Department of Psychiatry and Behavioral Sciences at the University of Southern California is seeking a Clinical Project Manager to support NIH- and foundation-funded clinical research programs ...
Los Angeles, CA ยท Hybrid
The Department of Psychiatry and Behavioral Sciences at the University of Southern California is seeking a Clinical Project Manager to support NIH- and foundation-funded clinical research programs ...
Qualifications Bachelor's degree, preferably in the life science or related field, advanced degree preferred. 5+ years or relevant project management of clinical trials experience managing all ...
Qualifications Bachelor's degree, preferably in the life science or related field, advanced degree preferred. 5+ years or relevant project management of clinical trials experience managing all ...
Support Clinical Project Manager / Director in completing clinical project management activities; support activities throughout all phases of a clinical project, including any SOP-required ...
Support Clinical Project Manager / Director in completing clinical project management activities; support activities throughout all phases of a clinical project, including any SOP-required ...
Qualifications Bachelor's degree, preferably in the life science or related field, advanced degree preferred. 5+ years or relevant project management of clinical trials experience managing all ...
Qualifications Bachelor's degree, preferably in the life science or related field, advanced degree preferred. 5+ years or relevant project management of clinical trials experience managing all ...
As Clinical Project Manager, you will own the planning, execution, and oversight of assigned clinical studies, working cross-functionally with clinical operations, regulatory, data science, and ...
As Clinical Project Manager, you will own the planning, execution, and oversight of assigned clinical studies, working cross-functionally with clinical operations, regulatory, data science, and ...
$22.5K - $31.7K
1% of jobs
$31.7K - $41K
4% of jobs
$41K - $50.2K
11% of jobs
$54.5K is the 25th percentile. Wages below this are outliers.
$50.2K - $59.4K
18% of jobs
The median wage is $66.3K / yr.
$59.4K - $68.6K
21% of jobs
$68.6K - $77.9K
16% of jobs
$81.2K is the 75th percentile. Wages above this are outliers.
$77.9K - $87.1K
11% of jobs
$87.1K - $96.3K
6% of jobs
$96.3K - $105.5K
5% of jobs
$105.5K - $114.8K
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$114.8K - $124K
3% of jobs
$22.5K
$72.5K
$124K
| Aspect | Junior Clinical Project Manager | Clinical Trial Coordinator |
|---|---|---|
| Credentials | Bachelor's degree in life sciences; some roles prefer project management certification | Bachelor's degree in life sciences or related field |
| Work Environment | Manages multiple projects, collaborates with teams, oversees timelines | Supports trial activities, manages documentation, coordinates with sites |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Research sites, hospitals, CROs |
| Common Search & Comparison | Often compared for entry-level project management roles in clinical trials | Often 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.

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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Recruiting and staffing services
11 - 50 Employees
Manchester, NH, US
2008