Clinical Research Coordinator (PRN Days)

Trinity Health•Silver Spring, MD

8d•$28 - $44•Hybrid

About The Position

The Clinical Research Coordinator coordinates pharmaceutical company, National Cancer Institute (NCI), multisite and in-house protocol activities for the Cancer Program and principal investigators. Adheres to federal regulations, sponsor guidelines, medical center policies and procedures; and performs related work as required. Supports the Mission of Trinity Health and Holy Cross Hospital.

Requirements

Bachelor’s Degree required
Good Clinical P actice (GCP) Certification (preferred).
Basic Life Support (BLS) Certification.
Clinical research certification (preferred).
Active Driver’s License.
Knowledge of cancer and clinical protocols.
Three years or more experience in research program leadership.
3-5 years related clinical research and project management experience.
Ability to communicate effectively, both orally and in writing.
Ability to create and conduct presentations to public and professional audiences.
Ability to analyze and synthesize data, prepare and present reports as necessary.
Ability to maintain patient confidentiality.
Ability to understand federal regulations and translate those regulations to guide the research work.
Ability to facilitate and lead a multidisciplinary team of professionals involved in research studies.

Nice To Haves

Master’s Degree in a health-related field
Good Clinical Practice (GCP) Certification
Clinical research certification

Responsibilities

Coordinates pharmaceutical company, National Cancer Institute (NCI), multisite and in-house protocol activities for the Cancer Program and principal investigators.
Adheres to federal regulations, sponsor guidelines, medical center policies and procedures.
Performs related work as required.
Supports the Mission of Trinity Health and Holy Cross Hospital.