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Sr Clinical Data Manager Jobs in Rochester, MI (NOW HIRING)

TH Medical

Senior Clinical Auditor

Detroit, MI · On-site

$80K - $98K/yr

Identifies new services and technology in the clinical setting and facilitates establishment of new ... management. [BRASSRING IMPORT 11/11/16] Minimum Qualifications 1.Bachelor's Degree in Nursing. 2.

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Alcanza

Data Entry Coordinator

Farmington, MI

Managing data entry into computer systems for clinical trials, including entering patient data into eDC and other software * Reviewing patient charts and other medical records to ensure data is ...

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All JobsSr Clinical Data JobsSr Clinical Data Manager JobsSr Clinical Data Manager Jobs in Rochester, MI

Sr Clinical Data Manager information

See Rochester, MI salary details

$72.7K

$113.3K

$169.8K

How much do sr clinical data manager jobs pay per year?

As of Aug 15, 2026, the average yearly pay for sr clinical data manager in Rochester, MI is $113,266.00, according to ZipRecruiter salary data. Most workers in this role earn between $96,200.00 and $126,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Sr Clinical Data Manager?

To thrive as a Sr Clinical Data Manager, you need expertise in clinical data management, knowledge of regulatory requirements (such as GCP and FDA), and typically a degree in life sciences or related fields. Proficiency with data management systems like Medidata Rave, Oracle Clinical, and experience with CDISC standards or relevant certifications are commonly required. Strong project management, leadership, and communication skills help you effectively oversee teams and ensure data quality. These skills and qualifications are crucial for ensuring accurate, compliant, and timely clinical trial data that supports successful regulatory submissions.

What does a Sr Clinical Data Manager do?

A Sr Clinical Data Manager oversees the collection, management, and quality control of clinical trial data. Their responsibilities include designing data collection systems, ensuring data accuracy and integrity, managing databases, and coordinating with clinical research teams. They play a critical role in ensuring that clinical data meets regulatory standards and is ready for analysis and submission. Typically, Sr Clinical Data Managers also mentor junior staff and help develop data management protocols and best practices.

What are some typical challenges a Sr Clinical Data Manager might face when overseeing multiple clinical trials simultaneously?

A Sr Clinical Data Manager often manages several trials at once, which can lead to challenges such as coordinating data collection across diverse study sites, ensuring consistent data quality, and meeting tight regulatory deadlines. Balancing these demands requires strong organizational skills, proactive communication with cross-functional teams, and effective delegation of tasks to junior data managers. Staying updated on evolving data standards and regulatory requirements is also crucial to avoid delays or compliance issues.

What job categories do people searching Sr Clinical Data Manager jobs in Rochester, MI look for?

The top searched job categories for Sr Clinical Data Manager jobs in Rochester, MI are:

What cities near Rochester, MI are hiring for Sr Clinical Data Manager jobs?

Cities near Rochester, MI with the most Sr Clinical Data Manager job openings:

Sr Clinical Data Manager jobs near you
Infographic showing various Sr Clinical Data Manager job openings in Rochester, MI as of August 2026, with employment types broken down into 85% Full Time, 10% Part Time, and 5% Contract. Highlights an 78% In-person, and 22% Remote job distribution, with an average salary of $113,266 per year, or $54.5 per hour.

Senior Clinical Research Coordinator

DM Clinical Research

Detroit, MI

$24 - $32/hr

Full-time

Re-posted 25 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