Projects & Compliance Manager

Taketalent

is partnering with

PharmaMar

, a leading biopharmaceutical company dedicated to the

research, development, and production of innovative oncology therapies

, to find a

Regulatory Affairs Project Manager

with an

international scope

This is a

hybrid position

, ideal for professionals eager to manage strategic regulatory projects globally and contribute to the success of end-to-end innovative products.

The selected candidate

will play a key role in managing

regulatory submissions, global regulatory strategies, and cross-functional coordination

, ensuring that projects meet the highest scientific and regulatory standards. Clinical Development, Medical Affairs, Pharmacovigilance, Quality, Manufacturing & Supply, Legal, Business Development, and Commercial. Contribute to defining

global regulatory strategies

, identifying risks and opportunities. Review clinical and scientific documentation to ensure regulatory compliance. Manage regulatory databases and collaborate on

international regulatory strategies

• . Supervise CROs and work effectively with

global project teams

Degree in Health Sciences (PhD, MSc, or MBA preferred). Fluent in English, both written and spoken. Industry experience : at least 3 years in Regulatory Affairs and Project Management within the biopharmaceutical sector. Management of regulatory deliverables at the project level Knowledge of Business and processes in the pharmaceutical industry Highly Valued : Global knowledge in CMC, preclinical, and clinical development Competitive salary + performance-based bonus. Benefits package (private health insurance, stock plan, continuous training, company cafeteria, etc.). Flexible working hours with short Fridays. Opportunity to contribute to a

leading oncology company with global impact

regulatory affairs with international scope

, we would be delighted to receive your application.