Data Coordinator

Job Description

Job Description

Join the world's largest early phase oncology clinical research network! The START Center for Cancer Research is revolutionizing cancer treatment through groundbreaking clinical trials that bring hope directly to patients. With an impressive global footprint spanning the United States, Spain, Portugal, and Ireland, we've completed over 1,300 studies that have led to 43 FDA/EMA approved therapies—including being the first to treat a patient with Keytruda, the most effective cancer drug in medical history. Unlike traditional Academic Medical Centers that reach only 20% of cancer patients, START brings cutting-edge trials directly to community hospitals where most patients receive care. By joining our team, you'll be part of an organization that's truly changing lives and shaping the future of cancer treatment worldwide. Learn more at STARTresearch.com.

We are hiring a motivated Data Coordinator for our Grand Rapids, Michigan location who will collect, enter/transcribe, and transmit/submit clinical data for assigned investigational drug studies. This position operates during standard business hours of 8:30 AM - 5:00 PM .

Essential Responsibilities

• Manage clinical data through collection, entry, and submission in electronic/paper case report forms (CRFs)
• Process and resolve data queries while ensuring accuracy and completeness
• Obtain necessary patient records from study teams to complete documentation requirements
• Coordinate monitor visits and participate in exit meetings to review data
• Identify and communicate lab facility information to Regulatory Affairs staff
• Maintain current data entry across all assigned studies
• Attend key study meetings including initiations, monitor exits, and audit preparations
• Support on-site audit activities as required
• Liaise with accounts receivable regarding submitted data

Education & Experience

• Bachelor's degree or equivalent experience in lieu of degree.
• Knowledge and training in general office administration skills, including computer applications, filing systems, etc.

Preferred Education and Experience

• Ability to accurately perform data review and CRF completion in its entirety with minimal direction.
• Familiarity with medical terminology.
• Additional demonstration of clinical research knowledge as evidenced by the use of either CCRP or CCRC credentials is highly desirable.

Physical and Travel Requirements

• Travel required up to 10% of the time.
• Sitting for extended periods of time.
• Typing and computer use for extended periods of time.

Best-in-Class Benefits and Perks

We value our employees' time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

• Comprehensive health coverage: Medical, dental, and vision insurance provided
• Robust retirement planning: 401(k) plan available with employer matching
• Financial security: Life and disability insurance for added protection
• Flexible financial options: Health savings and flexible spending accounts offered
• Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
• Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.