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Clinical Research Coordinator for Investigational Products
2 months ago
Flourish Research is seeking dedicated and skilled individuals eager to advance their careers while contributing to impactful research. We provide a comprehensive benefits package, a collaborative work atmosphere, and numerous opportunities for professional development.
Position: Investigational Product Clinical Research Coordinator
The Investigational Product Clinical Research Coordinator (CRC) is responsible for the secure distribution of pharmaceutical supplies to participants, ensuring strict compliance with clinical trial protocols. This role encompasses managing medication inventory, preparing and administering medications, and meticulously documenting patient interactions and study data. The IP CRC works closely with other clinical research personnel, emphasizing patient safety, data accuracy, and adherence to regulations while ensuring an exceptional patient experience at every interaction.
Work Schedule: Monday-Friday, 8 AM - 5:30 PM
Compensation: Hourly Rate commensurate with experience + comprehensive benefits, paid time off, and 401k matching
*Overtime compensation for weekend, evening, or early morning work as required.
Key Responsibilities
- Represent Flourish Research with professionalism when engaging with staff, sponsors, Institutional Review Boards (IRBs), patients, and healthcare professionals.
- Conduct protocol-specific subject visits and procedures with precision.
- Document subject evaluations, observations, and test outcomes in accordance with regulatory and protocol standards.
- Support pharmaceutical services by managing, assembling, and distributing medications.
- Ensure pharmacy inventory, safety, and cleanliness by following established procedures and regulations.
- Organize and prepare medications for dispensing, including the assembly of intravenous solutions.
- Monitor and maintain drug storage conditions, report any discrepancies, and ensure medication availability.
- Complete required training and accurately document study-related activities.
- Maintain confidentiality of patient and protocol information in compliance with agreements and HIPAA regulations.
- Promptly report adverse events and Serious Adverse Events (SAEs) to appropriate supervisors.
- Manage clinical trial materials and maintain communication with key stakeholders.
- Stay informed on federal regulations and Flourish Research policies through ongoing training and educational opportunities.
- Perform all study-related duties efficiently, safely, and in compliance with Flourish Research policies.
- Bachelor's degree or equivalent experience in clinical research.
- Pharmacy Technician Certification is preferred.
- A minimum of 1 year of experience in clinical research.
- A minimum of 1 year of experience in a pharmacy environment.
- Basic understanding of research design, patient care, regulations, and medical terminology.
- Strong communication and interpersonal skills.
Flourish Research offers a comprehensive benefits package, a supportive and collaborative work environment, and numerous opportunities for professional growth. We are committed to enhancing the quality of life for communities globally.
Flourish Research is dedicated to fostering an inclusive and diverse workforce. We believe that diversity enriches our organization and enhances our ability to serve our communities effectively.
It is the policy of Flourish Research to ensure equal employment opportunities for all applicants and employees without regard to age, color, sex, disability, national origin, race, religion, or veteran status.
