Senior Clinical Affairs Project Manager Tracking Code 2005886 Job Description This position is responsible for the administration and project management of multiple Phase 1-4 clinical trials. The Sr Project Manager will be involved with research an...

The Director or Senior Director, Clinical Affairs is a tactical and leadership position that reports to the Vice President of Clinical and Regulatory Affairs and is responsible for devising, implementing and managing the clinical operations of multiple ph...

Pathway Medical Technologies, Inc., an innovator in the design and development of vascular medical products, is currently seeking a Manager of Clinical Affairs to join Pathway’s rapidly growing organization. The primary responsibility of this position ...

This is an outstanding opportunity for a Clinical Affairs manager.The company has new breakthrough medical device technology. The position will supervise the conduct of all clinical and preclinical studies designed to evaluate the performance, safety and ...

Successful candidate will be involved in all aspects of clinical trial conduct, including but not limited to: Preparing and distributing study materials such as case report forms (CRFs), study reference manuals, and monitoring guidelines...

Successful candidate will be responsible for the following: Prepare and maintain all regulatory documentation for Sponsor In coordination with Sponsor, schedule study-related meetings and training sessions; provide instru...

Successful candidate will provide administrative support to the Manager of Clinical Services which will include but is not limited to the following: Clinical contract assistance (typing, mailing, follow-up, tracking, etc) F...

A local (Boston, Ma. area) pharmaceutical company is seeking a VP of Clinical Development/MD to guide a program that will be a major asset to them. They have recently obtained a SPA from the FDA and will be starting a pivotal Phase III program. My clien...

Assists in the operational activities involved in the planning, conduct and completion of clinical trials. Uses some independent action and judgment to complete these activities. Such activities include: Establishing and ordering clinical supplies. Establ...

Assists in the operational activities involved in the planning, conduct and completion of clinical trials. Uses some independent action and judgment to complete these activities. Such activities include: Establishing and ordering clinical supplies Establi...

Responsible for participating in the operational activities involved in the planning, conduct, and completion of clinical trials (activities include ordering clinical supplies, collection review and filing of clinical trial and regulatory documentation, p...

3 Days Onsite / 2 Days working from home. Writing, editing Clinical Trial Reports. To include activities such as: Explaining tables from data output. Finding errors in tables and overall report. Providing quality control of clinical trial report or parts...

Responsible for participating in the operational activities involved in the planning, conduct, and completion of clinical trials (activities include ordering clinical supplies, collection review and filing of clinical trial and regulatory documentation, p...

Our client is a global science-based health care company with leading prescription and consumer products. The company develops, manufactures and markets advanced drug therapies to meet important medical needs. It strives to earn and maintain the trust o...