Job Description

Description

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.

Be Part of a Life-Changing Mission

We are seeking a passionate Clinical Research Coordinator for our Grand Rapids, MI location to join our team of dedicated professionals making a difference in cancer patients' lives. In this role, you'll be at the forefront of groundbreaking oncology research, directly contributing to treatments that offer hope to patients worldwide.

The Clinical Research Coordinator (CRC) supports the conduct of early-phase oncology clinical trials by managing daily study activities, ensuring protocol adherence, regulatory compliance, and patient safety. This role involves meaningful patient interaction, precise data collection, and coordination of multiple clinical trial protocols. The CRC works closely with our research team to implement and complete protocol-specific requirements, maintaining clear communication and accurate documentation throughout the trial process.

Schedule: Monday through Friday, 8am - 4:30pm, on site in Grand Rapids, MI 49546

Essential Responsibilities:

• Coordinate daily activities of assigned clinical trials, ensuring adherence to protocol requirements, Standard Operating Procedures (SOPs), and Good Clinical Practice (GCP) guidelines.
• Serve as the primary contact for Study Sponsors, CROs, and internal staff, addressing protocol-related questions, concerns, and status updates.
• Facilitate patient screening, informed consent, and eligibility determination in compliance with protocol standards.
• Prepare, manage, and maintain study documentation, including source documents, regulatory files, and protocol amendments.
• Identify and address protocol deviations, working with leadership and staff on corrective actions and ensuring thorough documentation.
• Collaborate with the Principal Investigator and data team on adverse event reporting, query resolution, and study closeout activities.

Education & Experience:

• High School Diploma or GED required.
• 2 years of clinical research experience.
• Basic understanding of oncology clinical trials, particularly Phase 1 studies.
• Strong attention to detail and accuracy in data collection and documentation.
• Ability to manage multiple tasks and meet deadlines in a fast-paced environment.
• Excellent organizational and time-management skills.
• Strong communication skills, both written and verbal.
• Ability to interact professionally with patients, study staff, and external stakeholders.
• Working knowledge of GCP and regulatory requirements.
• Proficient in Microsoft Office Suite and clinical trial management software.

Preferred Education and Experience:

• Experience working in an oncology setting.

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 STARTresearch.com.

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.

Job Tags

Full time, Local area, Worldwide, Flexible hours, Monday to Friday,

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