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 ...
Clinical Project manager
Marlborough, MA · On-site
$65/hr
Qualifications 4-5 years exp in a PM/Clinical environment. development of drugs in a PM Works with ... Often reports to product development, project management or marketing executives. Additional ...
Clinical Project manager
Marlborough, MA · On-site
$65/hr
Qualifications 4-5 years exp in a PM/Clinical environment. development of drugs in a PM Works with ... Often reports to product development, project management or marketing executives. Additional ...
Clinical Project Manager
Lexington, MA · On-site
This is a Clinical Integration Project Manager Manage Integration project team and project deliverables. Provide continuous support of integration activities. Manage and document integration team ...
Clinical Project Manager
Lexington, MA · On-site
This is a Clinical Integration Project Manager Manage Integration project team and project deliverables. Provide continuous support of integration activities. Manage and document integration team ...
Clinical Project Manager
Cambridge, MA · On-site
As Clinical Project Manager, you will be accountable for managing clinical studies that will lead the biopharma industry in speed and quality of clinical study design and execution. You will be an ...
Clinical Project Manager
Cambridge, MA · On-site
As Clinical Project Manager, you will be accountable for managing clinical studies that will lead the biopharma industry in speed and quality of clinical study design and execution. You will be an ...
Clinical Project Manager
Cambridge, MA · On-site
As Clinical Project Manager, you will be accountable for managing clinical studies that will lead the biopharma industry in speed and quality of clinical study design and execution. You will be an ...
Clinical Project Manager
Cambridge, MA · On-site
As Clinical Project Manager, you will be accountable for managing clinical studies that will lead the biopharma industry in speed and quality of clinical study design and execution. You will be an ...
Lexington, MA Position- Senior Clinical Project manager Job Summary: The candidate will be responsible for supporting the operational, planning, and decision-making processes within Client s Early ...
Lexington, MA Position- Senior Clinical Project manager Job Summary: The candidate will be responsible for supporting the operational, planning, and decision-making processes within Client s Early ...
Clinical Project Manager III Location: Lexington, MA, United States Duration: 06+ Months Job Details: Responsible for the planning, implementation, execution and management of one or more complex ...
Clinical Project Manager III Location: Lexington, MA, United States Duration: 06+ Months Job Details: Responsible for the planning, implementation, execution and management of one or more complex ...
Clinical Research Associate
Lexington, MA · On-site
The in-house Clinical Research Associate (CRA) is responsible for providing support for day to day clinical study activities under general supervision of the the Clinical Project Manager(s). The CRA ...
Clinical Research Associate
Lexington, MA · On-site
The in-house Clinical Research Associate (CRA) is responsible for providing support for day to day clinical study activities under general supervision of the the Clinical Project Manager(s). The CRA ...
Clinical Research Associate
Lexington, MA · On-site
Manages escalation of study related issues and communicates as appropriate with Clinical Project Manager. * Responsible for the operational oversight of the Clinical CRO with regards to data feed ...
Clinical Research Associate
Lexington, MA · On-site
Manages escalation of study related issues and communicates as appropriate with Clinical Project Manager. * Responsible for the operational oversight of the Clinical CRO with regards to data feed ...
Clinical Project Associate
Cambridge, MA · On-site
$61K - $87K/yr
Partner with Clinical Project Managers to support the day-to-day operations of clinical trial execution, with a focus on site start-up, study participant enrollment, clinical monitoring, GCP and ...
Clinical Project Associate
Cambridge, MA · On-site
$61K - $87K/yr
Partner with Clinical Project Managers to support the day-to-day operations of clinical trial execution, with a focus on site start-up, study participant enrollment, clinical monitoring, GCP and ...
The Clinical Domain Project Manager plans, coordinates, and delivers pharmacy clinical initiatives within a Medicaid, pharmacy benefit management (PBM), and healthcare payer environment. This role ...
The Clinical Domain Project Manager plans, coordinates, and delivers pharmacy clinical initiatives within a Medicaid, pharmacy benefit management (PBM), and healthcare payer environment. This role ...
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... Data Management, TMF Operations, etc.) * Oversee regional startup and feasibility activities ...
Quick apply
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... Data Management, TMF Operations, etc.) * Oversee regional startup and feasibility activities ...
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... Data Management, TMF Operations, etc.) * Oversee regional startup and feasibility activities ...
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... Data Management, TMF Operations, etc.) * Oversee regional startup and feasibility activities ...
Project Manager I (Clinical) Job Location: Northborough, MA Duration - 12 +Months Client- Sanofi (5831400) Duties: Manages the Demand for Packaging & Distribution of Investigational Products for ...
Project Manager I (Clinical) Job Location: Northborough, MA Duration - 12 +Months Client- Sanofi (5831400) Duties: Manages the Demand for Packaging & Distribution of Investigational Products for ...
The position collaborates with Principal Investigators, the Center Manager, and the Registry Project Manager to support the successful implementation of the Center's clinical research program. Core ...
The position collaborates with Principal Investigators, the Center Manager, and the Registry Project Manager to support the successful implementation of the Center's clinical research program. Core ...
The position collaborates with Principal Investigators, the Center Manager, and the Registry Project Manager to support the successful implementation of the Center's clinical research program. Core ...
The position collaborates with Principal Investigators, the Center Manager, and the Registry Project Manager to support the successful implementation of the Center's clinical research program. Core ...
Clinical Research Project Manager - Breast Oncology
Boston, MA · On-site +1
$76K - $85K/yr
The Clinical Research Project Manager is responsible for the day-to-day coordination and management of Breast Oncology clinical trial activities, primarily focusing on multi-center, PI-initiated ...
Clinical Research Project Manager - Breast Oncology
Boston, MA · On-site +1
$76K - $85K/yr
The Clinical Research Project Manager is responsible for the day-to-day coordination and management of Breast Oncology clinical trial activities, primarily focusing on multi-center, PI-initiated ...
As the Project Manager, Clinical Research - New Site Build at Iterative Health for the Cardiology service line, you will lead the end-to-end execution of opening new Cardiology research sites from ...
As the Project Manager, Clinical Research - New Site Build at Iterative Health for the Cardiology service line, you will lead the end-to-end execution of opening new Cardiology research sites from ...
The Role Associate Director, Clinical Supplies Project Management is responsible for oversight and leadership of clinical supply activities for a program and/or a clinical study. The scope includes ...
The Role Associate Director, Clinical Supplies Project Management is responsible for oversight and leadership of clinical supply activities for a program and/or a clinical study. The scope includes ...
Clinical Supply Associate
Lexington, MA · On-site
Manages clinical supplies inventory for projects assigned by interfacing with contractor to ensure that inventory systems are kept up to date and that final product reconciliation is completed. MUST ...
Clinical Supply Associate
Lexington, MA · On-site
Manages clinical supplies inventory for projects assigned by interfacing with contractor to ensure that inventory systems are kept up to date and that final product reconciliation is completed. MUST ...
Internship Clinical Project Manager information
See Boston, MA salary details
$31.60 - $39.43
16% of jobs
$45.49 is the 25th percentile. Wages below this are outliers.
$39.43 - $47.27
12% of jobs
$47.27 - $55.10
14% of jobs
The median wage is $60.33 / hr.
$55.10 - $62.94
13% of jobs
$62.94 - $70.77
15% of jobs
$74.36 is the 75th percentile. Wages above this are outliers.
$70.77 - $78.61
13% of jobs
$78.61 - $86.44
4% of jobs
$86.44 - $94.28
5% of jobs
$94.28 - $102.11
5% of jobs
$102.11 - $109.95
1% of jobs
$109.95 - $117.78
2% of jobs
$31
$65
$117
How much do internship clinical project manager jobs pay per hour?
As of Sep 2, 2026, the average hourly pay for internship clinical project manager in Boston, MA is $65.95, according to ZipRecruiter salary data. Most workers in this role earn between $45.96 and $77.31 per hour, depending on experience, location, and employer.
What does an internship clinical project manager do?
An Internship Clinical Project Manager assists with the planning, coordination, and execution of clinical trials under the supervision of senior project managers. They may help with study documentation, scheduling meetings, communicating with stakeholders, and ensuring compliance with regulatory standards. Interns in this role gain hands-on experience with the daily operations of clinical research and learn about the processes required to bring new medical treatments to market.
What kinds of projects and responsibilities can I expect as an internship clinical project manager?
As an Internship Clinical Project Manager, you will typically assist with the planning, coordination, and execution of clinical trials under the guidance of senior project managers. Your daily tasks may include tracking project timelines, supporting documentation and regulatory submissions, scheduling meetings, and communicating with cross-functional teams such as data management, regulatory affairs, and clinical operations. This role provides valuable exposure to the full clinical study lifecycle and offers mentorship opportunities, giving you hands-on experience that can support your future career growth in clinical project management.
What are the key skills and qualifications needed to thrive as an internship clinical project manager, and why are they important?
To thrive as an Internship Clinical Project Manager, you need foundational knowledge of clinical research, project management principles, and a relevant degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Microsoft Office Suite, and regulatory guidelines such as GCP is typically required. Strong organizational skills, effective communication, and the ability to collaborate in cross-functional teams are valuable soft skills. These competencies ensure efficient project execution, regulatory compliance, and seamless teamwork in managing clinical studies.
What is the difference between Internship Clinical Project Manager vs Clinical Research Coordinator?
| Aspect | Internship Clinical Project Manager | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Typically pursuing or holding a degree in life sciences, with some certifications like CCRP or PMP | Often holds a bachelor's degree in health sciences or related field; certifications like CCRP are common |
| Work Environment | Manages clinical trials, oversees project timelines, and collaborates with teams in research settings | Coordinates daily clinical trial activities, interacts directly with patients and site staff |
| Employer & Industry Usage | Used in pharmaceutical companies, CROs, and research institutions during internship programs | Commonly employed in hospitals, research centers, and clinical trial sites |
The Internship Clinical Project Manager role focuses on overseeing clinical trial projects during an internship, involving planning and coordination. In contrast, the Clinical Research Coordinator handles the day-to-day operations at trial sites, ensuring protocol adherence and patient management. Both roles require knowledge of clinical research processes but differ in scope and responsibilities.
What are the most commonly searched types of Clinical Project Manager jobs in Boston, MA?
The most popular types of Clinical Project Manager jobs in Boston, MA are:
Job description
Company Description
At Mindlance, we strive to deliver value through the combination of right people, processes, technologies and program management solutions. Our methods include- applying domain expertise in specific industry segments, utilizing a highly-skilled workforce, leveraging a proven global delivery model, implementing structured and scalable quality processes and methodologies and yet, staying cost-effective
All in all, our expertise lies in providing trained and committed minds to help meet your business objectives, irrespective of the stage your business is in.
Job Description
Job Position: 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 to moderate complexity or defined activities in more complex, multicenter studies (e.g., managing niche vendors). The Clinical Project Manager will be able to ensure study timelines and milestones are met and studies completed according to the protocol.  Â
Manages clinical project team members to appropriate and timely completion of projects; oversees project timeline development and maintenance.  Â
Internally interfaces with data management and biostatistics, regulatory affairs, clinical compliance, field clinical monitors, medical directors, liaison with investigators and clinical site staff.
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 to moderate complexity or defined activities in more complex, multicenter studies (e.g., managing niche vendors). The Clinical Project Manager will be able to ensure study timelines and milestones are met and studies completed according to the protocol.  Â
Manages clinical project team members to appropriate and timely completion of projects; oversees project timeline development and maintenance.  Â
Internally interfaces with data management and biostatistics, regulatory affairs, clinical compliance, field clinical monitors, medical directors, liaison with investigators and clinical site staff.
Qualifications
Requirement:
Essentially they need to be able to run a clinical study Owning the time, budget, running the team meetings, making sure that the other functional groups are reporting updates, handling study sites, handling vendor oversight (these are the main components)
 At least three years of Study Management (actually running the study) is needed.
 Pharma experience OR working on the vendor side for clinical research organization (and have a pharma client) that is OK.
Bachelors required
Essentially they need to be able to run a clinical study Owning the time, budget, running the team meetings, making sure that the other functional groups are reporting updates, handling study sites, handling vendor oversight (these are the main components)
 At least three years of Study Management (actually running the study) is needed.
 Pharma experience OR working on the vendor side for clinical research organization (and have a pharma client) that is OK.
Bachelors required
Additional Information
Regards
___________________________________________________________________________________________________
Pooja Mishra | Team Recruitment | Mindlance, Inc. | Office: 732-243-0715
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996