descrizione del lavoro

Unlock Your Potential with Thermo Fisher Scientific

We're a global organization committed to accelerating research, solving complex scientific challenges, and driving technological innovation. Our Mission is to enable our customers to make the world healthier, cleaner, and safer.

About the Role

We have an exciting opportunity for an experienced Medical Writing Program Manager to join our team in Bulgaria and/or Serbia. As a key member of our Clinical Trials group, you will be responsible for leading patient-centric medical writing programs, managing complex projects, engaging with clients, and ensuring flawless delivery and quality of documents.

Your Key Responsibilities

">
• Develop and adapt project plans and timelines to meet client expectations;
">
• Engage and manage client relationships to ensure satisfaction and loyalty;
">
• Collaborate with cross-functional teams to deliver high-quality documents on time;
">
• Mentor junior staff and ensure compliance with quality processes;
">

What We Offer

You'll discover meaningful work that makes a positive impact on a global scale. Our flexible working culture values a work-life balance, and we offer a comprehensive benefits package that prioritizes your health and well-being. Join us and become part of a collaborative environment where colleagues share expertise and have fun together.

Requirements

To succeed in this role, you'll need:

">
• Advanced project management skills with experience managing medical writing or clinical projects;
">
• Outstanding planning and organizational abilities with a focus on delivering high-quality documents on time;
">
• Excellent communication, negotiation, and decision-making skills with the ability to engage and manage client relationships;
">
• In-depth knowledge of regulatory and document development guidelines;
">
• Proven ability to lead and mentor junior staff while ensuring compliance with quality processes;
">

Education and Experience

We're looking for candidates with a BS/BA (preferably in a scientific field) with a minimum of 8 years of relevant experience or an advanced degree with a minimum of 6 years of relevant experience. Ideally, you'll have experience working in the pharmaceutical/CRO industry and preferably in medical writing (Regulatory and/or plain language).

We're an Equal Opportunities Employer

We value diversity and inclusion and welcome applications from talented individuals who share our commitment to making the world a better place. If you're passionate about delivering quality and accuracy while improving health outcomes, we encourage you to apply for this exciting opportunity.