CRC Specialist (Remote)

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval.

The START Center for Cancer Research is seeking a CRC Specialist to be responsible for leading the operational startup of new START USA sites by providing hands-on coordination and training in Phase I oncology trials. This role will temporarily fill the CRC role at launch sites, guide and mentor new CRC hires, and ensure the seamless execution of study start-up activities and early operations. In addition, this role will support existing START sites by covering CRC responsibilities during vacancies, ensuring no disruption in patient care or study conduct.

This is a remote role with an annual base salary for this role is $80,000 - $100,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience.

Essential Responsibilities

• Act as the interim CRC at new START sites during launch phase, managing study start-up, patient enrollment, and clinical coordination duties.
• Train and mentor the first on-site CRC at each new location, ensuring comprehensive onboarding to START SOPs, GCP compliance, and study-specific procedures.
• Serve as a trusted expert and role model for new and tenured CRCs across START USA.
• Travel to START sites as needed (approximately 50%) to support launch operations or in-person support for struggling sites.
• Support existing sites by covering CRC responsibilities during periods of leave, turnover, or unexpected staffing gaps.
• Collaborate with Study Operations leadership, Quality Assurance, and HR on continuous improvement of training programs and SOP implementation.
• Ensure protocol compliance, timely documentation, and coordination of patient-related activities for assigned studies, whether in-person or remote.
• Communicate effectively with site staff, investigators, sponsors, CROs, and patients to maintain study continuity and data integrity.
• Identify process inefficiencies or gaps and contribute to site-level or organizational CAPAs and workflow redesign initiatives.
• Participate in study start-up meetings, monitor protocol amendments, and ensure staff are trained on changes.
• Support implementation of best practices in patient consenting, AE/SAE documentation, and data collection across sites.
• Maintain expert-level understanding of current and evolving GCP, FDA, and institutional regulatory requirements.

Required Education and Experience:

• High School Diploma or GED.
• 5 years of clinical research experience, with deep expertise in Phase I oncology trials.
• Proven record of successfully coordinating multiple complex protocols and mentoring other research staff.
• Exceptional communication, leadership, and training abilities.
• Demonstrated success in implementing quality improvement initiatives or standardization efforts.
• Strong command of clinical trial documentation, patient-facing procedures, and regulatory frameworks.
• Ability to travel up to 50% to various START USA locations as needed.
• Experience using clinical trial management systems (CTMS), EMRs, and sponsor IRT platforms.

Preferred Education and Experience:

• Bachelor’s degree.
• Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP).
• More than 5 years of experience in a lead CRC or trainer role within an oncology research setting.
• Formal training in adult learning principles or prior experience developing training materials.

Physical & Travel Requirements:

• 50% travel expected across U.S. sites for onsite coverage or training.
• When not traveling, work will be conducted remotely or at a START facility.
• Fast-paced, high-pressure environment with shifting priorities.
• Must be comfortable adapting to different site cultures and workflows.

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.