Job 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.
We are hiring an
Administrative Research Assistant at our START Midwest office located in
Grand Rapids, MI . This role will assist the Clinical Research Coordinators in all tasks to support their roles. It will require an understanding of research terminology and basic protocol interpretation.
Hours : Monday through Friday 8:00 – 4:30
Hybrid schedule : On site 50% - variable on site schedule, days may vary each week
Essential Responsibilities - Collect, de-identify, enter, and submit clinical data in paper/electronic case report forms (CRFs), including query resolution for assigned studies.
- Collaborate with the Clinical Research Coordinator to ensure accurate data timepoints and resolve queries.
- Contact patients for follow-up as needed per protocol.
- Maintain study documentation, including Eligibility, Study Schedules, Flow Sheets, and CTMS updates (patient visits, IRB re-consents, SAEs, and Deviations).
- Support onsite and remote monitors, ensuring timely data transmissions.
- Comply with all regulations, guidelines, and procedures for data entry and EDC systems.
- Attend study-related meetings and communicate with accounts receivable staff as needed.
Required Education and Experience: - High School diploma or equivalent.
- One year of research administrative experience within a healthcare, pharmaceutical, or research organization.
- Knowledge and training in general office administration skills, including computer applications, filing systems, etc.
- Familiarity with medical terminology.
- Strong organizational skills and a sense of timeliness in completing projects.
- Must be detail-oriented and able to understand instructions and work independently.
Preferred Education and Experience: - Knowledge and training in general office administration skills, including computer applications, filing systems, etc.
- Familiarity with medical terminology.
- Strong organizational skills and a sense of timeliness in completing projects.
- Must be detail-oriented and able to understand instructions and work independently.
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.
Job Tags
Full time, Local area, Worldwide, Flexible hours, Monday to Friday,