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Depression Research Coordinator Study Jobs (NOW HIRING)

IQVIA

Research Coordinator

Houston, TX

Research Coordinators attend study teleconferences with sponsors and clinical research organizations to assure continuity of information. Essential Duties and Responsibilities Essential and other ...

IQVIA

Research Coordinator

Irving, TX

Research Coordinators attend study teleconferences with sponsors and clinical research organizations to assure continuity of information. Essential Duties and Responsibilities Essential and other ...

IQVIA

Research Coordinator

Irving, TX

Research Coordinators attend study teleconferences with sponsors and clinical research organizations to assure continuity of information. Essential Duties and Responsibilities Essential and other ...

DaVinci Research

Clinical Research Coordinator

Roseville, CA · On-site

$25.50 - $33.75/hr

The Clinical Research Coordinator will be involved in the coordination and execution of clinical ... Responsibilities include managing study documentation, overseeing site-specific trial activities ...

Dartmouth College

Research Coordinator

Hanover, NH · On-site

The Research Coordinator will play a key role in Digital Biomarkers of Postoperative Pain study. This five-year, NIH-funded trial will use ecological momentary assessment (EMA), wearable biosensor ...

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Depression Research Coordinator Study information

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How much do depression research coordinator study jobs pay per year?

As of Sep 10, 2026, the average yearly pay for depression research coordinator study in the United States is $54,853.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $62,500.00 per year, depending on experience, location, and employer.

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Infographic showing various Depression Research Coordinator Study job openings in the United States as of June 2026, with employment types broken down into 93% Full Time, 6% Part Time, and 1% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $54,853 per year, or $26.4 per hour.

Senior Clinical Research Coordinator

Detroit, MI • On-site

DM Clinical Research
11 - 50 employees
Learn more about DM Clinical Researchexternal

$24 - $32/hr

Full-time

Re-posted 21 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