Job Description

Job Description

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 a Clinical Research Coordinator for our San Antonio location. The Clinical Research Coordinator Lead will be assigned multiple protocols at any time for which they will oversee the aspects of assigned protocols with planning and coordinating patient participation in the trial. They are responsible for implementation as well as completion of protocol specific requirements and will provide accurate, up to date information to all team members involved with any aspect of carrying out protocol specific requirements. They will understand the ethical issues involved in human subjects’ research, adhering to the Federal Regulations governing research.

Essential Responsibilities

• Process Improvement & Compliance : Identify and execute process improvements, ensuring compliance with GCP guidelines, CAPAs, and SOPs.
• Sponsor & Study Collaboration : Serve as the primary contact for sponsors/CROs on assigned studies, facilitating study conduct and attending all study-related meetings.
• Protocol & Study Oversight : Monitor day-to-day study conduct, implement protocol amendments, and train staff on protocol compliance.
• Patient Intake & Consent : Support patient screening, eligibility determination, and facilitate the informed consent process.
• Documentation & Reporting : Maintain study files, manage source documents, and assist with Serious Adverse Event reporting and protocol closeout activities.
• Communication & Collaboration : Communicate effectively with internal teams and external sponsors to ensure timely responses and study data integrity.

Education & Experience

• Education : Bachelor’s degree or equivalent education and experience
• Experience : Two years hospital/clinic pharmacy experience. Prior experience in clinical trials and management of investigational drugs preferred. Minimum of 5 years of patient and/or clinical team member experience, oncology preferred. Additional demonstration of clinical research knowledge as evidenced by the use of either CCRP or CCRC credentials is highly desirable

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

Local area, Remote job, Worldwide, Flexible hours,

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