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Senior Clinical Research Associate

Houston, TX · Hybrid

Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

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$36K

$94.3K

$143.5K

How much do senior clinical research jobs pay per year?

As of Jul 19, 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, and why are they important?

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.

More about Senior Clinical Research jobs
What cities are hiring for Senior Clinical Research jobs? Cities with the most Senior Clinical Research job openings:
What are the most commonly searched types of Clinical Research jobs? The most popular types of Clinical Research jobs are:
What states have the most Senior Clinical Research jobs? States with the most job openings for Senior Clinical Research jobs include:
What job categories do people searching Senior Clinical Research jobs look for? The top searched job categories for Senior Clinical Research jobs are:
Senior Clinical Research jobs near you
Senior Clinical Research Coordinator

Senior Clinical Research Coordinator

DM Clinical Research

Detroit, MI

$24 - $32/hr

Full-time

Re-posted 29 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.

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