Offer summary

Qualifications:

Bachelor's degree in life sciences, English, or a related field., Strong writing and editing skills with attention to detail., Experience in medical writing or a related field is preferred., Familiarity with regulatory guidelines and clinical research processes..

Key responsibilities:

Develop and write clinical study reports, protocols, and other regulatory documents.

Collaborate with researchers and medical professionals to gather information.

Ensure all documents meet quality standards and regulatory requirements.

Participate in meetings with clients to discuss project progress and requirements.

Founded in 2001, Envision Pharma Group is a leading global technology-enabled strategic solutions partner for the life sciences industry, working with over 200 pharma and biotech companies, including 18 of the top 20 pharmaceutical companies. Envision supports clients across the product life cycle through a comprehensive suite of services and industry-leading technology solutions that include artificial intelligence and natural language processing, commercialization and integrated strategic consulting, evidence-based scientific communications, and engagement, HEOR/market access and data analytics, medical capabilities, and omnichannel solutions.

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