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

... clinical, and member data to surface actionable insights that reduce cost of care and improve ... senior stakeholders, including Chief Actuaries - Play a key role in the development of new ...

Data Architect

Auburn Hills, MI ยท On-site

$60.25 - $77.50/hr

This role will work under the direct leadership of the Senior Manager for Enterprise Data Architecture. Knowledge of industry-standard Business Intelligence software and Data Integration Management ...

Data Architect

Auburn Hills, MI ยท On-site +1

$60.25 - $77.50/hr

Position Description The Senior Enterprise Data Architect will be responsible for designing and implementing solutions within Business Intelligence and Data Management software and hardware to meet ...

Data Architect

Auburn Hills, MI ยท On-site +1

$60.25 - $77.50/hr

Position Description The Senior Enterprise Data Architect will be responsible for designing and implementing solutions within Business Intelligence and Data Management software and hardware to meet ...

Data Architect (Remote)

Auburn Hills, MI ยท Remote

$65.25 - $84/hr

Position Description The Senior Enterprise Data Architect will be responsible for designing and implementing solutions within Business Intelligence and Data Management software and hardware to meet ...

Showing results 21-40

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 Sep 7, 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 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 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 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:

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, 13% Part Time, 1% Contract, and 1% Nights. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $113,266 per year, or $54.5 per hour.

Unblinded Clinical Research Coordinator II (4021)

DM Clinical

Southfield, MI โ€ข On-site

$22.25 - $29.50/hr

Other

Re-posted 8 days ago


Job description

DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator II to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials. Pharmacy Technicians, LPN's and CMA's are encouraged to apply!
Duties & Responsibilities:
  • Compound and dispense prescribed IP as needed by Sponsor approved protocol
  • Study IP management
  • Provide training and guidance for new team members
  • Assist in all aspects of company start up activities as required
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans
  • Perform regular audits on the clinical data to assess percent completeness and accuracy
  • Assist in onboarding training for new members
  • Ensure external sites' regulatory documents and required site certifications are up to date
  • Provide consultative support regarding the preparation and dosing of drugs
  • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction
  • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials
  • Understand and apply all applicable site procedures
  • Ensure receipt and proper storage of IP and bioretention samples, including temperature reporting
  • Develop operating procedures, guides and best practices for data entry portals and project workflows
  • Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure all aspects of protocols and study requirements are understood.
  • Any other duties or tasks assigned by the manager

KNOWLEDGE & EXPERIENCE
Education:
  • Associates Degree required or 2 years of formal educational coursework
  • Bachelor's degree, preferred
  • Secondary or Foreign Medical Graduate, preferred

Experience:
  • 2+ years of Clinical Research experience, inclusive of in-clinic experience, required
  • 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required
  • 1+ year utilizing CRIO, preferred

Credentials:
  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant), preferred
  • Pharmacy Technician Certification, preferred
  • Completion of DMCR-required training, including GCP, OSHA and IATA

Knowledge and Skills:
  • Computer proficiency, especially Word, Excel, Outlook, and Google Suite products.
  • Excellent communication and customer service skills, both written and verbal
  • Excellent time-management skills
  • Ability to remain composed under pressure and high-stress situations
  • Outgoing personality
  • Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred