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Manager Of Clinical Research Jobs (NOW HIRING)

DaVinci Research

Clinical Research Coordinator

Roseville, CA · On-site

$25.50 - $33.75/hr

... of clinical trials, including obtaining informed consent, ensuring compliance with study protocols, and facilitating research staff communication. Responsibilities include managing study ...

Tekton Research Inc

Clinical Research Coordinator

Wichita, KS · On-site

$21.50 - $28.75/hr

Clinical Research Coordinator (CRC) About Tekton Research: Tekton Research is a growth-oriented ... Coordinate and manage all aspects of assigned clinical trials from study start-up through close-out.

Headlands Research

Clinical Research Manager

Escondido, CA · On-site

$100K - $105K/yr

As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and ... The Role The Clinical Research Manager combines the responsibilities of supporting the coordination ...

Washington University of St. Louis

$75K - $128K/yr

Responsible for the management of the Division of Clinical Research and the day-to-day functions of the division. * Responsible for recruiting, hiring, managing and review of clinical research staff ...

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How much do manager of clinical research jobs pay per year?

As of Aug 23, 2026, the average yearly pay for manager of clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What does a manager of clinical research do?

A Manager of Clinical Research oversees the planning, execution, and management of clinical trials within a healthcare or pharmaceutical organization. They ensure studies comply with regulatory requirements, manage research staff, and coordinate communication between sponsors, regulatory agencies, and investigators. Additionally, they are responsible for maintaining budgets, timelines, and quality standards throughout the research process. Their goal is to ensure clinical trials are conducted ethically and effectively to generate reliable data for developing new treatments or therapies.

What are the key skills and qualifications needed to thrive as a manager of clinical research?

To thrive as a Manager of Clinical Research, you need a solid background in clinical trial management, regulatory compliance, and data analysis, typically supported by a degree in life sciences and experience in clinical research. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRA or CCRP are highly valued. Leadership, problem-solving, and effective communication are crucial soft skills for coordinating teams and collaborating with stakeholders. These competencies ensure the successful execution of studies, regulatory adherence, and the integrity of clinical data.

What are some common challenges faced by a manager of clinical research, and how can they be addressed?

A Manager of Clinical Research often encounters challenges such as coordinating multi-site studies, ensuring regulatory compliance, and managing diverse teams of clinical staff. Balancing strict timelines with the need for meticulous data collection and participant safety is also a frequent hurdle. These challenges can be addressed by fostering clear communication among team members, implementing robust project management tools, and staying updated on ever-evolving regulatory requirements. Building strong relationships with investigators and stakeholders can further streamline study operations and help proactively resolve potential issues.

How much do managers of clinical research make in the US?

Managers of clinical research in the US typically earn a median annual salary of around $90,000 to $130,000, depending on experience, education, and location. They often hold advanced degrees and certifications, such as RAC or CCRP, and oversee clinical trials, ensuring compliance and data integrity.

What cities are hiring for Manager Of Clinical Research jobs?

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Manager Of Clinical Research jobs near you

Unblinded Clinical Research Coordinator II

DM Clinical Research

Jersey City, NJ

$25.25 - $33.75/hr

Full-time

Re-posted 12 days ago

Job description

Unblinded Clinical Research Coordinator
DM Clinical Research, the largest privately-owned clinical research organization in the Houston area and one of the top fifty in the country, is looking for an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties amp; Responsibilities:
  • Compound and dispense prescribed IP.
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans.
  • Provide consultative support regarding the preparation and dosing of drugs.
  • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction.
  • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials.
  • Understand and apply all applicable site procedures.
  • Ensure receipt and proper storage of IP and bioretention samples.
  • Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
  • Review protocols and provide input on clinical and pharmacy supply needs.
  • Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information.
  • Temperature reporting.
  • Any other duties/ tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Foreign Medical Graduate is a plus
  • Pharmacy Technician Certification a plus
Experience:
  • Clinical Experience
Credentials:
  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant)
Knowledge and Skills:
  • Computer proficiency, especially Word, Excel, Outlook, and Google Docs.
  • Excellent communication and customer service skills.
  • Outgoing personality Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred but not required
DM Clinical Research, the largest privately-owned clinical research organization in the Houston area and one of the top fifty in the country, is looking for an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties amp; Responsibilities:
  • Compound and dispense prescribed IP.
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans.
  • Provide consultative support regarding the preparation and dosing of drugs.
  • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction.
  • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials.
  • Understand and apply all applicable site procedures.
  • Ensure receipt and proper storage of IP and bioretention samples.
  • Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
  • Review protocols and provide input on clinical and pharmacy supply needs.
  • Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information.
  • Temperature reporting.
  • Any other duties/ tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Foreign Medical Graduate is a plus
  • Pharmacy Technician Certification a plus
Experience:
  • Clinical Experience
Credentials:
  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant)
Knowledge and Skills:
  • Computer proficiency, especially Word, Excel, Outlook, and Google Docs.
  • Excellent communication and customer service skills.
  • Outgoing personality Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred but not required

Apply