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Clinical Research Consulting Jobs (NOW HIRING)

TriHealth

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

Functioning as an educator, consultant/liaison, and evaluator, the Clinical Research Coordinator strives to coordinate clinical research trials with safety, integrity and efficiency while applying ...

Vitalief

Clinical Research Coordinator

Newark, NJ · On-site

$65K - $78K/yr

ABOUT VITALIEF Vitalief is a consulting firm built exclusively for the research and clinical trial industry, providing innovative Consulting and Functional Service Provider (FSP) solutions to ...

Vitalief

Clinical Research Coordinator

Newark, NJ · On-site

$65K - $78K/yr

ABOUT VITALIEF Vitalief is a consulting firm built exclusively for the research and clinical trial industry, providing innovative Consulting and Functional Service Provider (FSP) solutions to ...

Actalent

Clinical Research Coordinator

Phoenix, AZ

$58K - $68K/yr

Job Title: Clinical Research Coordinator This role offers an opportunity for an experienced ... With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and ...

Eisenhower

Clinical Research Coordinator

Rancho Mirage, CA · On-site

$24.75 - $32.75/hr

Research-Cardiology Job Objective: Coordinates and implements clinical research activities ... consultation/expert advice to leadership.12. Develops or contributes to the development of SOPs ...

Vitalief

Clinical Research Nurse

New Brunswick, NJ · On-site

ABOUT VITALIEF Vitalief is a consulting and professional services firm that partners with clinical research sites, sponsors, and CROs to enhance trial activation, operational performance, and ...

Vitalief

Clinical Research Nurse

New Brunswick, NJ · On-site

ABOUT VITALIEF Vitalief is a consulting and professional services firm that partners with clinical research sites, sponsors, and CROs to enhance trial activation, operational performance, and ...

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Clinical Research Consulting information

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$49K

$107.3K

$189K

How much do clinical research consulting jobs pay per year?

As of Aug 10, 2026, the average yearly pay for clinical research consulting 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 professionals in clinical research consulting, and how can they be addressed?

Clinical Research Consultants often encounter challenges such as navigating complex regulatory requirements, balancing the needs of multiple stakeholders, and adapting to changing study protocols. Staying current with regulatory updates, maintaining clear communication with clients and research teams, and developing strong organizational skills are key strategies for overcoming these challenges. Additionally, consultants benefit from building a robust professional network to share insights and best practices, which helps ensure study compliance and successful project delivery.

What is clinical research consulting?

Clinical research consulting involves providing expert guidance and support to organizations or investigators conducting clinical trials and research studies. Consultants help with protocol development, regulatory compliance, study design, data management, and ensuring that research follows ethical and legal standards. They play a key role in optimizing study processes, navigating complex regulations, and improving the quality and efficiency of clinical research projects.

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 clinical research methodologies, regulatory compliance, and a relevant life sciences degree—often complemented by experience in clinical trials. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) certification, and data analysis tools is typically required. Exceptional communication, problem-solving, and organizational skills help consultants build client trust and navigate complex regulatory environments. These competencies are crucial for ensuring ethical, efficient, and successful research outcomes that meet both client expectations and industry standards.

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

AspectClinical Research ConsultingClinical Research Associate
CredentialsTypically requires a degree in life sciences, clinical research certifications (e.g., CCRP, CCRA)Requires a degree in life sciences; certifications like CCRA or RAC are common
Work EnvironmentConsultants often work independently or with consulting firms, providing expert advice to multiple clientsWorks directly on clinical trial sites or with sponsors, monitoring trials
Employer & Industry UsageUsed by consulting firms, CROs, or as independent contractors in the clinical research industryEmployed by pharmaceutical companies, CROs, or clinical trial sites

While both roles require similar educational backgrounds and certifications, Clinical Research Consulting involves providing expert advice and strategic guidance across multiple projects, often independently. In contrast, a Clinical Research Associate focuses on monitoring and managing specific clinical trial sites to ensure compliance and data integrity.

More about Clinical Research Consulting jobs
What cities are hiring for Clinical Research Consulting jobs? Cities with the most Clinical Research Consulting job openings:
What states have the most Clinical Research Consulting jobs? States with the most job openings for Clinical Research Consulting jobs include:
What job categories do people searching Clinical Research Consulting jobs look for? The top searched job categories for Clinical Research Consulting jobs are:
Clinical Research Consulting jobs near you
Infographic showing various Clinical Research Consulting job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Unblinded Clinical Research Coordinator II (4076)

DM CLINICAL RESEARCH GROUP

Brooklyn, NY • On-site

$25.75 - $34.25/hr

Full-time

Posted 2 days ago

New

Job description

DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator II to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.
Duties & Responsibilities:

  • Compound and dispense prescribed IP as needed by Sponsor approved protocol
  • Study IP management
  • Provide training and guidance for new team members
  • Assist in all aspects of company start up activities as required
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans
  • Perform regular audits on the clinical data to assess percent completeness and accuracy
  • Assist in onboarding training for new members
  • Ensure external sites’ regulatory documents and required site certifications are up to date
  • 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, including temperature reporting
  • Develop operating procedures, guides and best practices for data entry portals and project workflows
  • Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure all aspects of protocols and study requirements are understood.
  • Any other duties or tasks assigned by the manager
  •  

KNOWLEDGE & EXPERIENCE


Education:

  • Associates Degree required or 2 years of formal educational coursework
  • Bachelor's degree, preferred
  • Secondary or Foreign Medical Graduate, preferred

Experience:

  • 2+ years of Clinical Research experience, inclusive of in-clinic experience, required
  • 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required
  • 1+ year utilizing CRIO, preferred


Credentials:

  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant), preferred
  • Pharmacy Technician Certification, preferred
  • Completion of DMCR-required training, including GCP, OSHA and IATA


Knowledge and Skills:

  • Computer proficiency, especially Word, Excel, Outlook, and Google Suite products.
  • Excellent communication and customer service skills, both written and verbal
  • Excellent time-management skills
  • Ability to remain composed under pressure and high-stress situations
  • Outgoing personality
  • Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred

Apply