We’re expanding our network of domain experts to support ongoing and upcoming projects with leading global pharma and life sciences companies. If you are an experienced professional looking for flexible or contract-based opportunities, we’d love to hear from you.

Roles & Expertise Areas

We’re seeking skilled professionals across:

Regulatory Affairs
Pharmacovigilance (PV)
Clinical Research & R&D
Medical Writing & Publication Writing
Computer System Validation (CSV)
Data Science & Machine Learning (Life Sciences Analytics)

Key Responsibilities

Support project-based deliverables within your area of expertise
Collaborate cross-functionally with client and internal teams
Ensure compliance with industry standards, SOPs, and regulatory expectations
Contribute to documentation, data analysis, or scientific content development as applicable
Deliver high-quality, timely outputs aligned with project timelines

Qualifications

Bachelor’s / Master’s / PhD in Life Sciences, Pharmacy, Medicine, Biotechnology, or related fields
Relevant domain experience (3+ years minimum preferred)
Excellent communication and collaboration skills
Prior experience working in a contract / freelance capacity preferred

Freelance / Contract Professionals – Pharma & Life Sciences