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Clinical Research Consultant Jobs (NOW HIRING)

ARC Group

Medical Research Consultant

Jacksonville, FL · Remote

MEDICAL RESEARCH CONSULTANT REMOTE ARC Group has an immediate opportunity for a Medical Research ... clinical decision-support and medical policy-making organization within the enterprise, which ...

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How much do clinical research consultant jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for clinical research consultant in the United States is $39.38, according to ZipRecruiter salary data. Most workers in this role earn between $31.01 and $48.08 per hour, depending on experience, location, and employer.

How does a clinical research consultant typically collaborate with sponsors and clinical trial sites?

A Clinical Research Consultant acts as a bridge between sponsors, such as pharmaceutical companies, and clinical trial sites by ensuring that studies are conducted according to protocols, regulatory requirements, and timelines. They regularly communicate with site staff to resolve issues, provide training, and monitor progress. Consultants also facilitate the sharing of data and feedback, helping both sponsors and sites address challenges quickly and efficiently. This collaborative approach is essential for maintaining study integrity and meeting project milestones.

What are the key skills and qualifications needed to thrive as a clinical research consultant, and why are they important?

To thrive as a Clinical Research Consultant, you need a strong background in life sciences or healthcare, experience with clinical trial processes, and often an advanced degree such as a PharmD, PhD, or MD. Familiarity with regulatory compliance, clinical data management systems (like EDC), and certifications such as ACRP or SOCRA are highly valued. Excellent problem-solving, communication, and project management skills help consultants build trust with stakeholders and navigate complex studies. These competencies are crucial for ensuring ethical, efficient, and successful execution of clinical research projects.

What is the difference between Clinical Research Consultant vs Clinical Research Associate?

AspectClinical Research ConsultantClinical Research Associate
CredentialsTypically requires a degree in life sciences, clinical research certifications (e.g., CCRP), and industry experienceOften holds a degree in health sciences or related field, with certifications like CCRP or RAC
Work EnvironmentConsults with multiple clients or projects, often independently or as part of a consulting firmWorks directly on clinical trial sites or for sponsors, monitoring and managing trial activities
Employer & Industry UsageUsed by consulting firms, CROs, or as independent contractorsEmployed by pharmaceutical companies, CROs, or clinical sites

While both roles require similar credentials and industry knowledge, Clinical Research Consultants typically provide expert advice across multiple projects or organizations, whereas Clinical Research Associates focus on monitoring and managing specific clinical trials at trial sites.

Is a clinical research consultant a good career?

A clinical research consultant is a professional who manages and oversees clinical trials, ensuring compliance with regulatory standards and protocol adherence. The role typically requires strong analytical skills, knowledge of Good Clinical Practice (GCP), and relevant certifications, offering opportunities in healthcare, pharmaceuticals, and biotech industries. It can be a rewarding career for those interested in medical research and regulatory processes.

What does a clinical research consultant do?

A clinical research consultant provides expertise to design, implement, and oversee clinical trials to ensure they meet regulatory standards and scientific objectives. They analyze data, develop protocols, and advise on compliance, often working with sponsors, investigators, and regulatory agencies. Strong knowledge of Good Clinical Practice (GCP) and relevant software tools is essential for this role.

What qualifications do you need to be a clinical research consultant?

A clinical research consultant typically needs a bachelor's degree in a health-related field such as life sciences, nursing, or pharmacy. Relevant experience in clinical trials, knowledge of Good Clinical Practice (GCP), and strong communication skills are also important; some roles may require certification like the Certified Clinical Research Professional (CCRP).
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Clinical Research Consultant jobs near you
Infographic showing various Clinical Research Consultant job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $81,905 per year, or $39.4 per hour.

Unblinded Clinical Research Coordinator

DM Clinical Research

Philadelphia, PA

$24.50 - $32.50/hr

Full-time

Re-posted 28 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

Apply