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Senior Clinical Research Jobs (NOW HIRING)

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Senior Clinical Research Associate

Blue Bell, PA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior CRA/ CRA II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior CRA/ CRA II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

WEP Clinical

Senior Clinical Research Associate

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior CRA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation ...

Actalent

Senior Clinical Research Coordinator

Philadelphia, PA

$24.50 - $32.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Senior Clinical Research Coordinator - Oncology (Patient-Facing) This role focuses on coordinating and executing a wide range of oncology clinical trials within a breast disease group, with a strong ...

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Senior Clinical Research Associate

Blue Bell, PA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior CRA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation ...

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Senior Clinical Research information

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$36K

$94.3K

$143.5K

How much do senior clinical research jobs pay per year?

As of Aug 14, 2026, the average yearly pay for senior clinical research in the United States is $94,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $128,000.00 per year, depending on experience, location, and employer.

What are the typical challenges faced by senior clinical research professionals when overseeing multiple clinical trials?

Senior Clinical Research professionals often juggle multiple studies simultaneously, which can present challenges such as managing tight timelines, ensuring compliance with regulatory requirements, and coordinating cross-functional teams. Balancing these responsibilities requires strong organizational and communication skills, as well as the ability to adapt quickly to shifting project priorities. Effective collaboration with investigators, sponsors, and regulatory bodies is key to overcoming obstacles and ensuring the success of each trial.

What are the key skills and qualifications needed to thrive as a senior clinical research professional?

To thrive as a Senior Clinical Research professional, you need a strong background in clinical trial design, regulatory compliance, data analysis, and typically a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as Good Clinical Practice (GCP) are often required. Excellent leadership, problem-solving, and communication skills help drive project success and effective cross-functional collaboration. These skills and qualities are essential for ensuring the integrity, efficiency, and regulatory adherence of clinical research projects.

What is a senior clinical research professional?

A Senior Clinical Research professional is an experienced individual who oversees and manages clinical trials and research projects, often within the healthcare or pharmaceutical industries. They are responsible for ensuring studies comply with regulatory guidelines, managing study teams, designing protocols, analyzing data, and ensuring the safety and integrity of clinical trials. Typically, they serve as a liaison between sponsors, regulatory authorities, and research teams, and may also be involved in mentoring junior staff. This role requires a strong background in clinical research, regulatory knowledge, and leadership skills.

What is the difference between Senior Clinical Research vs Clinical Research Coordinator?

AspectSenior Clinical ResearchClinical Research Coordinator
Required CredentialsBachelor's degree, often advanced degrees, and experienceBachelor's degree, certification preferred
Work EnvironmentLeads projects, manages teams, oversees study progressSupports study activities, coordinates participant recruitment and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsResearch sites, hospitals, clinics
Common Search & ComparisonHigher-level responsibilities, project managementEntry to mid-level, operational focus

In summary, Senior Clinical Research professionals typically oversee entire studies, manage teams, and handle complex project aspects, requiring more experience and credentials. Clinical Research Coordinators focus on day-to-day study operations, participant management, and data collection, often serving as the operational backbone of clinical trials.

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Senior Clinical Research jobs near you
Infographic showing various Senior Clinical Research job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $94,314 per year, or $45.3 per hour.

Senior Clinical Research Coordinator

DM Clinical Research

Detroit, MI • On-site

$24 - $32/hr

Full-time

Re-posted 24 days ago

Job description

Senior Clinical Research Coordinator

Department
Clinical Operations - Detroit, MI
Employment Type
Full-Time
Minimum Experience
Experienced
DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for a Senior Clinical Research Coordinator experienced in coordinating studies for one of our research sites in Detroit, MI. This position works closely with our Clinical Research staff to provide excellent care to patients participating in our clinical trials.
Responsibilities:
  • Completing DMCR-required training, including GCP and IATA.
  • Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols.
  • Adhering to their assigned protocols at their respective site(s).
  • Maintain working knowledge of current FDA GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols.
  • Collecting source and submitting source per Sponsor requirements via the Sponsor-specified CRF system.
  • Completing Sponsor-required training prior to study-start, to include, but not limited to:
a. Sponsor provided and IRB approved protocol
b. All amendments
c. Investigator Brochure
d. Sponsor-specified EDC and/or IVRS
  • Continued recruitment and screening for their assigned protocols at their respective site(s) at all times as applicable
  • Being prepared for and available at all required company meetings and monitoring visits for their assigned protocols at their respective site(s).
  • Utilizing the most recent version of the Protocol, Informed Consent, and Investigator Brochures at their respective site(s).
  • Compiling and organizing all regulatory and administrative binders for their assigned protocols at their respective site(s) upon initial receipt of and wherever applicable.
  • Creating source documents for their assigned protocols at their respective site(s).
  • Conducting patient visits, and all other protocol-required procedures and documenting these in a timely manner.
  • Reporting all Adverse and Serious Adverse Events to the appropriate authorities per Sponsor, IRB, and ICH Guidelines.
  • Completing data entry and query resolution in a timely manner.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings.
  • Ensuring data quality in all trials being conducted at their respective site(s).
  • Addressing and resolving all issues from that monitor letters for all assigned protocols at their respective site(s) in a timely manner.
  • Striving to meet Sponsor goals for their assigned protocols at their respective site(s).
  • Strive to ensure weekly, monthly, and quarterly assigned goals are met for their respective site(s).
  • Any other matters as assigned by management.

Requirements:
  • Have at least three (5) years of experience as a CRC, preferably with practice coordinating industry sponsored trials in a private setting.
  • Foreign Medical Graduate a plus.
  • Be an energetic, go-getter who is detail-oriented and can multi-task.
  • Be goals-driven while continuously maintaining quality.
  • Have ACRP certification, which is a plus.
  • Bilingual in Spanish is a plus.

Apply