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Senior Clinical Research Associate Jobs in Rochester, MI

ICON

Clinical Research Associate

Detroit, MI · On-site +1

Clinical Research Associate - Oncology - Detroit, MI ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Icon plc

Clinical Research Associate

Detroit, MI

Clinical Research Associate - Oncology - Detroit, MI ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Spectrum Health

Clinical Research Coordinator II

Royal Oak, MI · On-site

$22.75 - $30.25/hr

CRT-Clinical Research Professional, Certified (CCRP) - SOCRA Society of Clinical Research Associates Upon Hire preferred Or * CRT-Clinical Research Coordinator, Certified (CCRC) - ACRP Association of ...

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Senior Clinical Research Associate information

See Rochester, MI salary details

$33.1K

$86.8K

$132.1K

How much do senior clinical research associate jobs pay per year?

As of Jul 17, 2026, the average yearly pay for senior clinical research associate in Rochester, MI is $86,812.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,500.00 and $117,800.00 per year, depending on experience, location, and employer.

How much does a CRA II make at Icon?

A CRA II (Clinical Research Associate II) at Icon typically earns between $70,000 and $90,000 annually, depending on experience, location, and certifications. Compensation may also include bonuses and benefits related to clinical trial monitoring and site management.

What is the role of a senior clinical research associate?

A senior clinical research associate (CRA) oversees the conduct of clinical trials to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. They monitor trial sites, review data quality, and coordinate with investigators, often using electronic data capture systems, and typically require relevant certifications and experience in clinical research. Their role is essential for maintaining trial integrity and ensuring timely study completion.

What are the key skills and qualifications needed to thrive as a Senior Clinical Research Associate, and why are they important?

To thrive as a Senior Clinical Research Associate, you need a solid background in clinical research, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong organizational skills, attention to detail, and the ability to communicate effectively with diverse stakeholders make someone stand out in this position. These skills and qualities are vital for ensuring studies are conducted ethically, accurately, and in compliance with regulatory standards.

What is the highest paying job in clinical research?

In clinical research, senior roles such as Director of Clinical Operations or Clinical Program Manager typically have the highest salaries, often exceeding $150,000 annually. These positions require extensive experience, leadership skills, and often advanced certifications or degrees in related fields.

What Does a Senior Clinical Research Associate Do?

A senior clinical research associate (CRA) monitors clinical trials and manages team members. Your duties include leading project team meetings, running experiments, making observations, tracking results, and analyzing data. You also ensure experiments meet all clinical practice and safety standards. Qualifications for this career are a bachelor of science in a biomedical field or a bachelor of science in nursing (BSN), along with professional experience in a medical or research setting. You must have strong communication, interpersonal, leadership, and technical writing skills.

How much does a senior CRA make at Iqvia?

A Senior Clinical Research Associate (CRA) at IQVIA typically earns between $80,000 and $110,000 annually, depending on experience, location, and certifications. The role often requires monitoring clinical trials, ensuring compliance, and working with clinical data management tools.

What are some typical challenges faced by Senior Clinical Research Associates when overseeing multiple clinical trials?

Senior Clinical Research Associates (SCRAs) often manage several studies at once, which requires balancing competing deadlines, ensuring protocol compliance, and maintaining strong communication with site staff. A common challenge is ensuring consistent data quality and regulatory adherence across diverse sites, especially when trials are geographically dispersed. Effective time management, attention to detail, and proactive problem-solving are crucial for success in this role. Collaboration with project managers, investigators, and regulatory teams is also essential to ensure trials progress smoothly and meet all regulatory requirements.

What is a Senior Clinical Research Associate?

A Senior Clinical Research Associate (Senior CRA) is an experienced professional responsible for overseeing and monitoring clinical trials to ensure compliance with regulatory requirements, protocols, and good clinical practice. They often serve as a liaison between the sponsor and clinical sites, ensuring data integrity and patient safety. Senior CRAs may also mentor junior staff, manage multiple studies, and resolve complex issues that arise during trials. Their work is critical in bringing new medical treatments and devices to market safely and efficiently.
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What job categories do people searching Senior Clinical Research Associate jobs in Rochester, MI look for? The top searched job categories for Senior Clinical Research Associate jobs in Rochester, MI are:
What cities near Rochester, MI are hiring for Senior Clinical Research Associate jobs? Cities near Rochester, MI with the most Senior Clinical Research Associate job openings:
Senior Clinical Research Associate jobs near you
Senior Clinical Research Coordinator

Senior Clinical Research Coordinator

DM Clinical Research

Detroit, MI • On-site

$24 - $32/hr

Full-time

Re-posted 26 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