Pharmaceutical Regulatory Affairs Jobs in Deerfield, IL

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Clinical Project Manager  

Randstad Life Sciences US - Lake Forest, IL, United States

cross-collaboration amongst functions involved in product launches (medical affairs, commercial/marketing, market access, clinical development, regulatory, etc.). Minimum 5+ years of full-time

from: linkedin.com - 21 days ago

HEOR Project Manager----Remote  

US Tech Solutions - North Chicago, IL, United States (+1 location)

launches (medical affairs, commercial/marketing, market access, clinical development, regulatory, etc.). Minimum 5+ years of full-time pharmaceutical industry or consulting experience in HEOR required

from: linkedin.com - 21 days ago

Regulatory Affairs Specialist II - Hybrid  

Primary Talent Partners - Round Lake, Illinois

within a pharmaceutical company, CRO, or similar organization. Strong understanding of FDA regulations and regulatory affairs practices related to medicinal products. Primary Talent Partners is an Equal

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from: resume-library.com - 2 days ago

Senior Consultant, Pharma/ Medical Device (Regulatory and M&A Consulting Solutions)  

Kamet Consulting Group - Chicago, IL, United States

of five years of work experience related to the Regulatory Affairs, Regulatory Operations, Supply Chain, or Labeling Operations within the pharmaceutical and/or medical device industry Prior consulting

from: linkedin.com - 21 days ago

Section Head - Medical Writing  

Abbott Laboratories - Chicago, Illinois

or Pharmaceutical. Training Required: Minimum 4 years relevant professional experience, in a related area such as R&D, Technical Product Development, Quality, Regulatory Affairs, Clinical Research, or Medical Writing

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from: resume-library.com - 2 days ago

Senior Scientific Director, International Medical Affairs- Oncology  

Mettawa, IL

stakeholders (e.g., commercial, clinical operations, market access, regulatory) as they relate to on-going medical affairs projects. Experience of leading successful teams in pharmaceutical medicine. Experience

from: Pharmadiversityjobboard.com - 17 days ago

Senior Scientific/Medical Director, Medical Affairs  

Mettawa, IL

of experience in Medical Affairs Ability to lead team and develop medical strategy independently with little supervision. Knowledge of clinical trial methodology, data analysis and interpretation, regulatory

from: Pharmadiversityjobboard.com - 23 days ago

clinical project manager iii (non-md)  

Randstad - lake forest, illinois

involved in product launches (medical affairs, commercial/marketing, market access, clinical development, regulatory, etc.). Minimum 5+ years of full-time pharmaceutical industry or consulting experience $90 - $104.42 per hour

from: randstadusa.com - 24 days ago

Scientific/Medical Director, Medical Affairs - Gastro Pipeline  

Mettawa, IL

in Medical Affairs with Global Medical Affairs experience highly preferred. Minimum of 4 years of clinical trials direct management experience in the pharmaceutical industry or academia or equivalent. 4+ years

from: Pharmadiversityjobboard.com - 24 days ago

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