Senior Regulatory Affairs / CMC Expert – FULL REMOTE
Our client is offering a unique opportunity for a seasoned Senior Regulatory Affairs / CMC Expert to join an esteemed organization that provides expert guidance and know-how for global pharma companies. With a proven track record of over 20 years, our client has successfully supported more than 1000 clients worldwide, addressing highly complex challenges and driving innovative approaches in drug development projects.
Benefits:
– Full-remote work arrangement for optimal work-life balance
– Competitive compensation package reflective of your expertise
– Opportunity to collaborate with the largest pharmaceutical companies globally
Responsibilities:
– Spearhead strategic collaborations with leading pharmaceutical players to advise on Regulatory Affairs / CMC in pioneering innovation projects
– Assume global responsibility in guiding cross-functional development teams for innovative drug development projects
– Engage in critical decision-making processes and contribute to the growth and success of the organization
Requirements:
– Advanced degree in life sciences, medicine, or veterinary medicine
– Minimum of 10 years of experience in pharmaceutical development
– Proven practical experience in strategic clinical development and regulatory strategy
Contact:
Julian #
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