Clinical Program Research Coordinator

  • Grand Rapids, MI
  • Permanent
  • Full-time
  • 23 days ago
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START’s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population – leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many – by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – the most effective cancer drug in medical history.We are hiring a motivated Clinical Program Research Coordinator supports oncology research through the XenoSTART Patient Xenograft Program by assisting with consent collection, biological sample handling, and coordination of research activities under the supervision of senior staff. This entry-level role is ideal for individuals with strong attention to detail, an interest in clinical research, and the ability to work independently while following established protocols.Essential Responsibilities
  • Patient Consent & Appointment Preparation
  • Travel to partner hospitals to obtain patient consents and deliver or collect samples using a company-approved vehicle.
  • Review the “patients of interest” list and coordinate with clinical teams to confirm scheduled appointments.
  • Sample Handling & Shipment
  • Collect and process fluid and tissue samples according to established biosafety procedures.
  • Label, package, and prepare biological samples for shipment following protocol.
  • Maintain accurate documentation for sample collections and shipments.
  • General Program Support
  • Ensure confidentiality and compliance with HIPAA and research regulations when handling patient information.
  • Collaborate with internal staff and external hospital personnel to ensure smooth handoff of consents and specimens.
Education & Experience
  • High school diploma required; associate’s degree preferred.
  • One (1) year of related experience in a research, clinical, or laboratory setting.
  • Strong attention to detail and commitment to accuracy.
  • Familiarity with basic specimen handling procedures and medical terminology a plus.
  • Good communication and interpersonal skills.
  • Proficiency in Microsoft Office applications preferred.
  • Ability to work both independently and collaboratively.
  • Valid driver’s license, clean driving record, and active auto insurance required.
Physical and Travel Requirements:
  • Travel: Required to travel up to 25% of the time
  • Sitting: Must be able to sit for extended periods of time.
  • Standing: Must be able to stand for extended periods of time.
  • Bending: Must be able to reach overhead, at shoulder level, or bend to perform tasks.
  • Lifting: Must be able to lift approx. 40 pounds.
  • Exposure: Works closely with physicians and ancillary personnel in caring for and treating oncology/hematology patients.
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.
More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at .Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

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