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Manager Clinical Research

Dallas, TX · On-site

  • Medical

  • Retirement

  • PTO

Directs financial oversight and management of clinical research unit; ensures invoicing is accurate and sponsor payments are received; ensures appropriateness of expenditures from various funding ...

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

As of Aug 14, 2026, the average yearly pay for manager clinical research organization 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 are some common challenges faced by a manager in a clinical research organization and how can they be addressed?

Managers in a Clinical Research Organization often encounter challenges such as balancing multiple concurrent clinical trials, ensuring regulatory compliance, and managing cross-functional teams. Effective communication and strong project management skills are essential to coordinate timelines, resources, and client expectations. Staying up-to-date with evolving industry regulations and fostering a collaborative team environment can help mitigate these challenges and ensure successful delivery of clinical studies.

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

To thrive as a Manager in a Clinical Research Organization, you need expertise in clinical trial management, regulatory compliance, and a relevant science or healthcare degree, often supplemented by experience in clinical operations. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and knowledge of GCP and ICH guidelines, as well as certifications like ACRP or SOCRA, are highly valued. Exceptional leadership, organizational, and communication skills help you coordinate multidisciplinary teams and manage complex projects effectively. These capabilities are crucial to ensuring the quality, timeliness, and regulatory adherence of clinical research studies.

What is a manager clinical research organization?

A Manager in a Clinical Research Organization (CRO) oversees the planning, execution, and management of clinical trials and research projects for pharmaceutical, biotechnology, or medical device clients. They coordinate teams of clinical research professionals, ensure compliance with regulatory standards, and manage budgets and timelines. Their role is critical in ensuring that clinical trials are conducted efficiently, ethically, and according to protocol, ultimately supporting the development and approval of new medical treatments.
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Manager Clinical Research Organization jobs near you
Infographic showing various Manager Clinical Research Organization job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Unblinded Clinical Research Coordinator

DM Clinical Research

Chicago, IL • On-site

$25 - $33.25/hr

Full-time

Re-posted 6 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

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