Medical affairs jobs in Upland, CA

Job Title. Medical Affairs Consultant I Duties. The Medical Information Specialist contractor candidate.. As a medical information product specialist, perform the following duties for assigned molecules..

In this role you'll perform a share of special clinical investigations and research as requested by the Senior Medical Director, Medical Affairs. These projects can include brief reviews of..

The Program Manager plans, organizes, directs, and manages all aspects of a mid to large scale recognized organizational program. Provides leadership, guidance, and direction for d..

Regulatory Affairs Manager. Permanent. San Francisco Bay Area Proclinical is seeking a Manager.. Advanced degree is preferred. 10. years of experience in medical device industry. 5. years of experience..

CM Medical are partnered with a exciting start up in the Heart Failure device space. We're seeking a.. Masters 8. years of experience in clinical affairs within the medical device industry, with a focus on..

Role. Regulatory Affairs Project Leader Location. Santa Clara, CA Duration. 12 Months Shift Timings.. Prior regulatory experience in the medical device, food, dietary supplement or pharmaceutical industry..

JCW is working on an exciting search for Regulatory Affairs Specialist III for global Biotech who is.. Bachelor's degree in life sciences or a related field 4. years of Regulatory Affairs experience in the..

We are supporting a small growing biotech in the Bay Area looking for a Senior Regulatory Affairs Associate! Education, Experience and Qualification Requirements. Bachelor's Degree in a..

JOB SUMMARY. The Principal Regulatory Affairs Specialist is responsible for developing and authoring.. The Principal Regulatory Affairs Specialist will understand the regulations governing medical devices..

Role. Director, Regulatory Affairs Bay Area Hybrid Company Description. This precision oncology biotech.. IND experience is wanted Oncology experience is a plus 8. years in Regulatory Affairs If you are..

Our client is looking for a VP of Clinical Affairs with a specialty in heart failure to lead on their.. Experience primarily in medical devices. Strong interpersonal skills and a savvy ability to interface..

Director, CMC Regulatory Affairs Direct Hire Full Time Role Salary Range. 208,000. 235,000 per year.. years of experience in global CMC regulatory affairs with working experience and content knowledge in..

They are looking to bring in an experienced Head of Regulatory Affairs. As they enter late stages of development it is key for them to find a Regulatory expert who can lead Health Authority..

JOB SUMMARY. The Principal Regulatory Affairs Specialist is responsible for developing and authoring.. The Principal Regulatory Affairs Specialist will understand the regulations governing medical devices..

Senior Director, Regulatory Affairs (Generalist) Remote Position for West Coast based candidates.. This position will be reporting into the SVP of Regulatory Affairs and will be supporting Clinical..

The successful candidate will play a crucial role in ensuring that our innovative medical device meets.. advanced degree preferred. Minimum of 5 7 years of experience in regulatory affairs within the medical..

Senior Regulatory Affairs Specialist Abbott is a global healthcare leader that helps people live more.. Free medical coverage for employees. via the Health Investment Plan (HIP) PPO. An excellent retirement..