ZipRecruiter

Log In

1

Clinical Research Consulting Jobs (NOW HIRING)

next page

Showing results 1-20

All JobsClinical Research Consulting Jobs

Clinical Research Consulting information

See salary details

$49K

$107.3K

$189K

How much do clinical research consulting jobs pay per year?

As of Aug 21, 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 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 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 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.

How to get into clinical research consulting?

To enter clinical research consulting, candidates typically need a background in life sciences, healthcare, or related fields, along with experience in clinical trials or regulatory processes. Gaining certifications such as Certified Clinical Research Professional (CCRP) or Regulatory Affairs Certification (RAC) can enhance prospects. Strong analytical skills, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems are also valuable.

What does a clinical research consulting do?

A clinical research consultant provides expertise to design, manage, and oversee clinical trials to ensure they meet regulatory standards and scientific objectives. They often assist with protocol development, regulatory submissions, and data analysis, using tools like electronic data capture systems. Strong knowledge of Good Clinical Practice (GCP) and relevant regulations is essential for this role.
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 100% Full Time. Highlights an 86% In-person, and 14% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Unblinded Clinical Research Coordinator

DM Clinical Research

Philadelphia, PA • On-site

$24.50 - $32.50/hr

Full-time

Re-posted yesterday

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