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Clinical Research Coordinator
The Start
Myrtle Beach, USA
Junior · 2+ years experience
Onsite
Discovered 1 weeks ago
gcp
Key Skills for This Role
gcp
Full Job Posting
Education & 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.
- Best-in-Class Benefits and Perks
- We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally:
- 401(k) retirement savings plan with employer match
- Eligibility for an annual performance bonus, based on role and company results
- Generous paid time off and paid holidays
- Comprehensive medical, dental, and vision coverage and optional insurance options
- Company paid life and disability insurance for added financial protection
- Employee Assistance Program (EAP) providing confidential, no ‐cost support for you and your family from day one
- Flexible FSA and HSA plans to support your financial wellness
- Commitment to a supportive environment that values balance, wellbeing, and flexibility
- We’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.
- More About START
- START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of “Hope Through Access”.
- 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.
Preferred Qualifications
- Eligibility for an annual performance bonus, based on role and company results
- Comprehensive medical, dental, and vision coverage and optional insurance options
About The Start
Biotechnology1000 employeesFounded 2007
Private early-phase oncology clinical research network serving cancer patients, physicians, and biopharma sponsors.
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