Project Manager
Date posted: April 7, 2008
Location: Raleigh, NC
Job type: Full-time
Industry: Pharmaceutical
Description:
Clinsys Clinical Research, Inc.® is a full-service clinical research organization (CRO) that provides pharmaceutical, biotechnology and medical device companies with a broad range of clinical research services in support of Phase I-IV drug and device development. Due to our continued growth we are seeking qualified candidates for the position of Project Manager for our North Raleigh office.
The Project Manager is responsible for the management and coordination of assigned activities associated with the conduct of clinical research trials sponsored by the pharmaceutical industry. These activities include the organization, planning, timely execution, reporting and evaluation of the clinical program objectives. Provides leadership to the project team, including office–based personnel and regional monitors. Serves as the primary contact with the sponsor for project related activities and a liaison with the monitors, clinical research sites, vendors and other internal departments such as Biometrics. Ensure that assigned projects proceed according to the designated timelines and within the approved budget. The Project Manager will develop new sponsor relationships and identify new business opportunities with current sponsors.
This position requires a bachelors degree or equivalent with preference in a bio-medical field (RN, RPh)or equivalent science degree. An advanced degree is desirable but not required. A Minimum of three years clinical trial experience is preferred. Experience in performing project management functions is required. Monitoring experience is mandatory. Candidates should have in-depth knowledge of the clinical trial and drug development process.
Category: Pharmaceutical/Biotech
Company: Clinsys Clinical Research, Inc.
Clinsys is a full-service clinical research organization (CRO) that provides pharmaceutical, biotechnology and medical device companies with a broad range of clinical research services in support of Phase I-IV drug and device development, including project management, clinical monitoring, scientific and medical support, investigator and patient recruitment, site management, biostatistics, data management, drug safety, quality assurance, regulatory affairs, and medical writing.