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 ...
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 ...
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 ...
Qualifications 4-5 years exp in a PM/Clinical environment. development of drugs in a PM Works with internal and external parties to initiate and run major projects. Coordinates schedules and ...
Qualifications 4-5 years exp in a PM/Clinical environment. development of drugs in a PM Works with internal and external parties to initiate and run major projects. Coordinates schedules and ...
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 ...
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH ...
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH ...
IQVIA Biotech is seeking an experienced Clinical Project Manager to lead and deliver innovative clinical trials in Internal Medicine . As a Project Manager, you'll drive operational excellence ...
IQVIA Biotech is seeking an experienced Clinical Project Manager to lead and deliver innovative clinical trials in Internal Medicine . As a Project Manager, you'll drive operational excellence ...
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 ...
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 ...
IQVIA Biotech is seeking an experienced Clinical Project Manager to lead and deliver innovative clinical trials in Internal Medicine . As a Project Manager, you'll drive operational excellence ...
IQVIA Biotech is seeking an experienced Clinical Project Manager to lead and deliver innovative clinical trials in Internal Medicine . As a Project Manager, you'll drive operational excellence ...
The in-house Clinical Research Associate (CRA) is responsible for providing support for day to day clinical study activities under general supervision of the Clinical Project Manager(s). The CRA also ...
The in-house Clinical Research Associate (CRA) is responsible for providing support for day to day clinical study activities under general supervision of the Clinical Project Manager(s). The CRA also ...
Proactively identify and resolve clinical project issues. * This role may require up to 25% travel Skills and experience you'll bring: * BS degree and 8+ years of experience in clinical operations in ...
Proactively identify and resolve clinical project issues. * This role may require up to 25% travel Skills and experience you'll bring: * BS degree and 8+ years of experience in clinical operations in ...
Associate Director, Clinical Operations
Watertown, MA · On-site
$175K - $195K/yr
Proactively identify and resolve clinical project issues. * This role may require up to 25% travel Skills and experience you'll bring: * BS degree and 8+ years of experience in clinical operations in ...
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Associate Director, Clinical Operations
Watertown, MA · On-site
$175K - $195K/yr
Proactively identify and resolve clinical project issues. * This role may require up to 25% travel Skills and experience you'll bring: * BS degree and 8+ years of experience in clinical operations in ...
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 ...
Interact with both internal and external customers and suppliers in order to accomplish project objectives. Develop IMP distribution and return drug plans and manage Clinical Supplies documentation ...
Interact with both internal and external customers and suppliers in order to accomplish project objectives. Develop IMP distribution and return drug plans and manage Clinical Supplies documentation ...
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 ...
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 ...
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 ...
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 Project information
What is a clinical project manager?
A Clinical Project Manager is a professional who oversees and coordinates all aspects of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They are responsible for planning, executing, and closing clinical research projects, ensuring that studies are completed on time, within budget, and in compliance with regulatory standards. Their role involves managing teams, collaborating with stakeholders, and handling documentation and reporting throughout the clinical trial process.
What are the key skills and qualifications needed to thrive as a clinical project manager?
To thrive as a Clinical Project Manager, you need a background in life sciences, experience in clinical research, and strong project management skills, often supported by a relevant degree and certification such as PMP or equivalent. Familiarity with clinical trial management systems (CTMS), regulatory compliance platforms, and data analysis tools is essential. Exceptional communication, leadership, and problem-solving skills set outstanding Clinical Project Managers apart. These skills and qualifications are crucial for ensuring clinical studies are conducted efficiently, compliantly, and within budget and timelines.
What are some common challenges faced by clinical project managers during multi-site clinical trials?
Clinical project managers often encounter challenges such as coordinating communication between diverse study sites, ensuring protocol compliance, and managing timelines across different geographic regions. Overseeing multiple teams requires strong organizational skills and adaptability, as unexpected issues like patient recruitment delays or regulatory changes can arise. Effective project managers proactively identify risks, foster collaboration among stakeholders, and regularly update sponsors to keep the trial on track.
What are the most commonly searched types of Clinical Project jobs in Massachusetts?
The most popular types of Clinical Project jobs in Massachusetts are:
What cities in Massachusetts are hiring for Clinical Project jobs?
Cities in Massachusetts with the most Clinical Project job openings:
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