Compliance Consultant (6 mo. Contract)

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma 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.

• Mid-level quality consultant to support document transition in TrackWise Digital (experience preferred, not required).
• 3000-5000 docs to revise, review, push training, etc.
• Doc control resource who has a quality background. Company currently operating under GCP, but GMP experience is ok.
• 40 hours/wk, 6 months. This is a Hybrid position requiring ~1 week per month onsite in Lake Forest, IL.