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Clinical Research Study Startup Jobs (NOW HIRING)

Medasource

Clinical Trial Budget Analyst

Sacramento, CA · On-site +1

$62/hr

The team works with investigators, study teams, sponsors, CROs, Contracts, Research Finance ... Supporting study startup and activation activities. * Ensuring alignment between clinical trial ...

WHOOP

Director, Clinical Research Operations

Boston, MA · On-site

Director, Clinical Research Operations As the Director, Clinical Research Operations, you will lead ... Lead study startup, planning, execution, monitoring, and closeout activities, ensuring timelines ...

Albany Medical College

$94K - $147K/yr

The Clinical Research Manager serves as the primary liaison between investigators, sponsors ... Oversee study startup activities including feasibility assessments, budget development, contract ...

Insight

Clinical Research Coordinator I (CRC-1)

Chicago, IL · On-site

$50K - $65K/yr

Coordinate site preparation, study startup, participant screening, enrollment, and follow-up visits ... Clinical research certification (CCRC, CCRP) eligible; certification expected within 18 months of ...

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Clinical Research Study Startup information

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$49K

$107.3K

$189K

How much do clinical research study startup jobs pay per year?

As of Sep 13, 2026, the average yearly pay for clinical research study startup 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 the difference between Clinical Research Study Startup vs Clinical Research Coordinator?

AspectClinical Research Study StartupClinical Research Coordinator
Primary RoleInitiates and prepares clinical trial sites for study activation, including regulatory submissions and site readiness.Manages daily trial activities at the site, including patient recruitment, data collection, and compliance.
Required CredentialsOften requires a bachelor's degree in health or life sciences; certifications like CCRP are common.Typically requires a bachelor's degree; certifications like CCRP or CRC are beneficial.
Work EnvironmentWorks closely with sponsors, CROs, and regulatory bodies during study startup phases.Works directly with patients, investigators, and site staff during the trial conduct.

While both roles are essential in clinical research, Study Startup focuses on preparing and initiating trials, whereas a Clinical Research Coordinator manages ongoing trial activities at the site.

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Clinical Research Study Startup jobs near you

Clinical Research Regulatory Coordinator - CNI

Camden, NJ

Cooper University Hospital
Health Care and Social Assistance • 5 - 10K employees
Learn more about Cooper University Hospitalexternal

$31 - $53/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 18 days ago

Cooper University Health Care rating

7.5

Company rating: 7.5 out of 10

Based on 133 frontline employees who took The Breakroom Quiz

Job description

At Cooper University Health Care, our commitment to providing extraordinary health care begins with our team. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. We have a commitment to our employees to provide competitive rates and compensation programs.  Cooper offers full and part-time employees a comprehensive benefits program, including health, dental, vision, life, disability, and retirement. We also provide attractive working conditions and opportunities for career growth through professional development.

Discover why Cooper University Health Care is the employer of choice in South Jersey.


  • The Clinical Research Regulatory Coordinator ensures regulatory compliance and accurate documentation for all clinical research studies conducted at Cooper University Health Care.
  • This role supports study startup, maintenance, and closeout by managing submissions to regulatory agencies, maintaining Investigator and staff documentation, and facilitating communication among Investigators, sponsors, and institutional offices. 

3-5 years required. 


Bachelor’s Degree required. Masters preferred. 


USD $31.00
USD $53.00

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