Clinical Trials Coord-Unlic.

This position is responsible for coordinating clinical research studies on human subjects. Responsible for subject recruitment, follow-up, data management, detailed record keeping and regulatory compliance, report writing, and correspondence with investigators, IRBs, and regulatory authorities. Responsible for the new submission of protocols with subsequent amendments. Some participation in protocol writing, and initial and continuing education for Good Clinical Practice compliance.

Practical research experience required (in a hospital setting) with a minimum of 3 years experience in the field.

* Experience in protocol assessment and implementation.
* Good organizational skills, detail-oriented, people-oriented, self-confident, flexible and adaptable to change, with time management skills. High energy level professional.
* Knowledge of protocols and its process.
* Must be able to relate cooperatively and constructively with personnel and co-workers.
* Experience with personal computers and basic software applications, including word processing, scheduling and contact database, email, web browsing, hospital records, other database software, and office equipment.
* Requires the ability to communicate effectively in English, both verbally and in writing, and to maintain confidentiality of sensitive information.
* Maintains knowledge of, and follows, relevant departmental and Stamford Hospital policies and procedures.
* Participates in mandated Stamford Hospital / Office of Research education / training initiatives
* Bachelor's Degree in scientific field required. RN preferred.
* Clinical research certification (such as CCRC, CCRP, CRA, IATA) preferred. If not yet certified, expected certification within 6-12 months of hire date.
* Human Research Subject Protection and Good Clinical Practice Certification
* OSHA training for handling hazardous biologic and chemical materials