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Location: Cayey, Puerto Rico
Schedule: 5 days per week, 8 hours/day (40 hours/week)
Hours: 7:00 AM – 3:30 PM (flexible), $18.00/HR
Position Overview: Under the supervision of the Director of Enterprise Programs and in partnership with the ASCP team, the Contract Study Coordinator Associate will manage day-to-day activities for the Associate Sample Donation Program (ASCP) at the Cayey PR location. This role includes:
Contacting and scheduling internal blood donors.
Clarifying collection requests.
Entering participant information into required databases.
Obtaining venous blood specimens by venipuncture.
Documenting daily draws.
Processing participant compensation.
Maintaining inventory of phlebotomy supplies and ensuring a clean and orderly work environment.
Qualifications:
Associate’s or Bachelor’s degree in a scientific discipline (preferably Nursing).
Experience working in a medical office or clinical laboratory.
1 year of phlebotomy experience is preferred.
Previous human subject research experience is a plus.
Valid Driver’s License and reliable transportation.
Experience and understanding of ethical and scientific quality standards for clinical research involving human subjects, including compliance with Good Documentation Practices (GDP) and Good Clinical Research Practice (GCP).
Strong interpersonal skills for effective communication.
Excellent time management and multi-tasking skills with attention to detail.
Ability to learn and utilize required databases and various software packages.
Proficiency in reading, writing, and verbally communicating in both English and Spanish.
Demonstrated ability to work well in a team and possess strong communication skills.
Additional Notes:
Manage a fast-paced environment with 1-11 participants per day.
Organize blood requestor’s schedules and demands.
Work with healthy adult volunteers and a vulnerable population.
Join Our Team! If you meet the qualifications and are interested in a dynamic and impactful role, apply now to become a vital part of our team. BD04123JD
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