Responsible for phlebotomy and other visit procedures in the conduct of clinical trials with emphasis on the safety and welfare of study participants. Assist Study Coordinators as needed. Perform the practical activities of clinical studies according to protocol, regulatory requirements, and SOPs.
Skills and Qualifications
- Previous phlebotomy, laboratory, medical office, or clinical experience preferred.
- Excellent organizational and time-management skills.
- Strong attention to detail and commitment to accuracy.
- Strong verbal and written communication skills.
- Excellent interpersonal skills and the ability to interact professionally and compassionately with study participants.
- Ability to maintain confidentiality and handle sensitive information appropriately.
- Ability to work collaboratively as part of a team while also taking direction and working independently.
- Self-motivated, dependable, and willing to learn new procedures and processes.
- Ability to effectively prioritize and manage multiple tasks in a fast-paced environment.
- Good computer skills and ability to learn and use electronic systems and research databases.
- Strong problem-solving and critical-thinking skills.
- Ability to follow detailed written and verbal instructions and adhere consistently to established protocols and procedures.
- Professional demeanor and commitment to providing a positive participant experience.
