Clinical Research Coordinator
2 months ago
The START Center for Cancer Research (“START”) is the world’s largest global phase I oncology clinical trial research site network. Over its 17-year history, START has provided hope to cancer patients in community practices and hospitals by offering access to cutting edge early phase oncology 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 tested at START facilities 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 is needed more now than ever before. There are nearly 20 million new cases of cancer per year across the globe, and 50% of all new clinical trials occur in cancer. Yet, AMCs are saturated with too many trials, too few patients, and not enough capacity to meet the demand. As a result, many of the trials in AMC settings take too long and do not reach patients in need. START offers hope to patients, while allowing clinical researchers to conduct essential trials and biopharma companies the ability to run trials on medicines. START’s legacy is rooted in scientific innovation. As an example, in San Antonio, where START was founded in 2007, START treated the first patient ever with Keytruda – the most effective cancer drug in medical history.
We are hiring for a Clinical Research Coordinator at our START Mountain Region location. The Clinical Research Coordinator is 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 assist in the maintenance of all study related Case Report Forms, whether paper or electronic as well as know status of completion. They will understand the ethical issues involved in human subjects research, adhering to the Federal Regulations governing research.
Essential Responsibilities:
Communicate on a regular basis with Study Sponsor’s, CRO’s, staff, etc. regarding questions, concerns, as well as status of the protocols
Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study
Review forms created or revised for assigned trials to assure protocol compliance
Maintain files using standardized study document labeling and filing procedures
Implement the initial protocol and amendments, training staff who will be involved in patient treatment and management
Assist with patient screening and determination of eligibility
Facilitate the informed consent process ensuring that consent is appropriately completed
Education & Experience:
Bachelor’s degree preferred; will consider experience in lieu of degree
Minimum of 2 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.
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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