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 motivated Clinical Research Coordinator (CRC) that will work on site in San Antonio, TX.

This role will work under the guidance of senior research staff to support the daily activities of early phase oncology clinical trials. The CRC ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards. This role involves direct patient interaction, data collection, and maintaining compliance with Good Clinical Practice (GCP). The Clinical Research Coordinator 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. Also, this role is responsible for implementation as well as completion of protocol specific requirements, providing accurate, up to date information to all team members involved with any aspect of carrying out protocol specific requirements.

Essential Responsibilities

• Communicate on a regular basis with Study Sponsor’s, CRO’s, staff, etc. regarding questions, concerns, as well as status of the protocol.  
• 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.  
• Create/review forms created or revised for assigned trials to assure protocol compliance.  
• Maintain files using standardized study document labeling and filing procedures.  
• Implement initial protocol and amendments, training staff who will be involved in patient treatment and management.  
• Maintain an up-to-date contact list.  
• Assist with patient screening and determination of eligibility.  
• Facilitate the informed consent process ensuring that consent is appropriately completed.  
• Prepare and manage source documents according to standard operating procedures.  
• Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations.   
• Assist data coordinator team with case report form completion and query resolution.  
• Work with the Principal Investigator to complete and submit Serious Adverse Event reports.  
• Perform protocol specific closeout related activities in conjunction with the data coordinator.  
• Provide documentation for all deviations whether related to the protocol or a SOP.  
• Ensure that all team members involved understand and adhere to assigned protocols.  

Required Education and Experience:

• High School Diploma or GED. 
• 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. 

Physical & Travel Requirements:

• Approximately 80% of time is spent sitting. 
• Very fast-paced and ever-changing healthcare environment. 
• Demanding deadlines and time frames. 
• Constant demand for updating knowledge. 
• Works closely with physicians and ancillary personnel in caring for and treating oncology/hematology patients. 

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, Work at office, Local area, Worldwide, Flexible hours,

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