Regulatory Sciences Expert

4 weeks ago


Cedar Springs, Michigan, United States ProPharma Group Full time

At ProPharma Group, we're committed to empowering biotech, med device, and pharmaceutical organizations to advance scientific breakthroughs and introduce new therapies.

As the world's largest RCO, we partner with our clients through an advise-build-operate model across the complete product lifecycle.

Our team of experts offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.

The RS Consultant plays a critical role in providing support to Project Managers, Scientific and/or Senior Staff as it relates to regulatory and scientific assignments.

Key Responsibilities:

  • Retrieve, research, and compile data to support client projects.
  • Conduct analysis of scientific data and regulatory information.
  • Summary regulatory information and pertinent scientific literature for assigned projects.
  • Ensure client-ready work product, on time and within budget.
  • Prepare populated templates for use by clients and/or internal project teams.
  • Communicate directly with clients, at the discretion of project managers/leads.
  • Support the strategic priorities and direction, as well as the day-to-day policies and practices, of the Company.
  • Actively participate and contribute to job creation marketing efforts within the Company.
  • Prepare and maintain Standard Operation Procedures (SOPs) for the research function.
  • Collaborate with peers and colleagues to develop knowledge of information sources and retrieval techniques.
  • Manage databases and regulatory communication logs.
  • May act as project manager on smaller assignments.

Requirements:

  • Excellent research skills.
  • Excellent verbal and written communication skills.
  • Proficient in MS Office with the ability to operate within database applications.
  • Detail-oriented, conscientious, and organized with the ability to multi-task and prioritize to manage deadlines.
  • Proficient in the use of technology tools and terminology.
  • Bachelor's Degree in a life science or related field of study.
  • 2+ years of regulatory or related experience.

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits.



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