The Role

We are looking for a Senior Clinical Research Coordinator to join our growing team. Under the supervision of the Site Director, the Senior Clinical Research Coordinator is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines. The Sr. Clinical Research Coordinator manages study conduct from planning through study closeout.

Responsibilities:

• In-depth understanding of Pharmaceutical Sponsor/Industry initiated FDA studies in order to conduct the study with excellent quality
• Managing all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending Investigator Meetings
• Providing the highest level of care for study patients and delivering excellent customer service to the Pharmaceutical clients
• Assist with lab draws, processing and shipping
• Some supervision of direct reports may be required
• Duties, responsibilities, and activities may change or new ones may be assigned at any time with or without notice

Requirements:

• Bachelors Degree preferred
• Minimum five plus (5+) years of experience as a Clinical Research Coordinator required
• Experience supervising other employees strongly preferred
• Medical assistant or phlebotomist required
• Commitment and ability to deliver excellent customer service
• Excellent communication, punctual and responsible
• Extremely well organized
• Excellent verbal and written communication skills
• Trustworthy, reliable; attentive to details
• Mature and pleasant demeanor
• Willingness to learn new tasks and grow with the company