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Clinical Trials Research Manager Jobs (NOW HIRING)

Wisconsin

Clinical Trials Research Coordinator

Madison, WI · On-site

$24.50 - $32.50/hr

The Department of Medicine (DOM) Clinical Trials team, within the DOM Office of Research Services ... The primary duties of this job involve the management of clinical research trial activity for ...

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Clinical Trials Research Manager information

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How much do clinical trials research manager jobs pay per year?

As of Sep 14, 2026, the average yearly pay for clinical trials research manager in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

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Clinical Trials Research Assistant

Edina, MN • On-site

Retina Consultants of Minnesota
51 - 200 employees
Learn more about Retina Consultants of Minnesotaexternal

$22 - $28/hr

Full-time

Medical, Dental, Life, PTO

Re-posted 18 days ago

Key responsibilities

  • Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines.

  • Observe, assist, collect, and record all necessary data for follow-up study visits, including adverse events and concomitant medications.

  • Transcribe subject study information from source documents to the Electronic Case Report Forms.

Job description

Description
We are seeking multiple outgoing, patient focused individuals to work as Clinical Trials Research Assistant at our Retina Consultants of Minnesota Edina, MN clinic.
Responsibilities for an Clinical Trials Research Assistant include:
  • Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines.
  • Prepare visit-specific documentation and charts for Clinical Research Coordinator
  • Observe Coordinator in patient care and management
  • Assist Coordinator in monitoring subject flow and assist in subject care and management
  • Observe, assist, collect and record all necessary data for follow up (e.g. adverse events, concomitant medications, etc.) study visits (Phase 2 & 3; NO Gene Therapy)
  • Transcribe subject study information from source documents to the Electronic Case Report Forms
  • Administer all mandatory questionnaires to study subjects
  • Set up, prepare subject, and conduct electrocardiograms (ECG) on subjects as required per study protocol
  • Promptly request all necessary medical records for Serious Adverse Event Reporting
  • Process and ship laboratory biological samples for analysis
  • Perform intraocular pressure checks after injections
  • Perform trial frame refraction and ETDRS visual acuity testing (For ISTs only, at selected sites)
  • Inform subjects and obtain written re-consents in regard to ICF's

Required Skills, Abilities and Attributes:
  • Applicants MUST be personally motivated to provide excellent patient care!
  • 1+ years of clinical trials research assistant experience in a retina or general ophthalmology environment preferred
  • Knowledge of medical terminology
  • Be an excellent team player who works cooperatively and respectfully with all doctors, supervisors and co-workers
  • Displays a desire to perpetually "Learn and Grow"
  • Efficient and highly accurate user of applicable information technology and health care management systems
  • High School Degree or GED

We offer excellent compensation and benefits, to include:
  • Paid Holidays - 7 days per year
  • Personal Time Off (PTO) - 16 days per year
  • Health Insurance
  • Health Reimbursement Account
  • Health Savings Account
  • Dental Insurance (free single coverage)
  • Flexible Spending Accounts
  • Basic and Supplemental Term Life Insurance (free single coverage)
  • Long Term Disability (free single coverage)
  • Long Term Care (free single coverage)
  • Short-Term Disability
  • Vision
  • Annual $250 uniform (scrubs and shoes) reimbursement

About Retina Consultants of Minnesota (RCM):
RCM has 9 Minnesota locations - St. Louis Park, Edina, Edina Specialty, Woodbury, Blaine, Duluth, Maplewood, Anoka and Mankato.
Everything we do.... every decision we make...takes our Guiding Principles into consideration. Our guiding principles are:
  • We exist to serve our patients. We will provide the best available medical skills, technology, and service. We will be their advocates. We will care for our patients as if they were members of our family. We will treat our patients with respect, dignity, and kindness.
  • We are proud of our dedicated staff. We will strive to provide a rewarding career with opportunity for personal and professional growth. We will promote teamwork. We will provide a respectful and safe working environment.
  • We are humbled that other doctors entrust their patients to our care. We will be available when we are needed. We will promptly communicate the results of patient evaluation and treatment. We will respect the referring doctors' relationships with their patients.
  • We recognize that we have a responsibility to our community. We will strive to be desire to perpetually "Learn and Grow"
  • Efficient and highly accurate user of applicable information technology and health care management systems
  • A good corporate citizen. We will function ethically. We will be prudent in our stewardship of healthcare resources.
  • Medical advances are critical to our patients. We will remain at the forefront in the search for new knowledge and treatments of retinal disease. We will participate in clinical research. We will share our knowledge with our patients and referring doctors, and with our retinal colleagues around the world.

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