Job Title: Clinical Research Coordinator

Positions available: (contract position)

Skills and Qualifications:

Nursing degree (B.S.) or related studies (Medical/Health/Science)
Pevious work experience working in a CRO/pharmaceutical industry
Knowledge of GCP/ICH and FDA regulations
Clinical trial experience
6 months clinical work experience (internship)
Strong research and project management skills
Intermediate computer knowledge

Duties Include :

Obtaining written informed consent and coordinating enrolment of study participants. You will be responsible for data collection ensuring accuracy and confidentiality of all data. You will collaborate with the health care team and participate in the general day to day activities of the study. You are responsible for communicating regularly with the multi-site research team and coordinating regular team meetings. You will be responsible for database management and for ensuring the accuracy, availability and security of all data. Other duties will include initial preparation and maintenance of study documents, maintaining a system for data abstraction, and initial data analysis and evaluation.

Previous experience with clinical trials and a sound knowledge of the research process and strong data management are highly desirable. The ability to work independently and within a team environment with excellent organizational, problem-solving & leadership skills are necessary. Strong interpersonal and communication skills are also necessary.

Email: info@excelstaffing.com