Senior Medical Writer (Line Management experience required)

The PrimeVigilance medical writer position offers a unique opportunity to further develop your career in the field of drug safety.

Key Responsibilities

• Independent authoring editing and reviewing of various regulatory / clinical documents (e.g. aggregate reports risk management plans and other documents needed throughout the products life cycle) with the responsibility for the quality and content of the document and compliance with internal and external standards
• Active participation in trainings and development implementation and maintenance of quality system documents for medical writing including internal templates and formats required for standardised documentation
• Support in all pharmacovigilance operations associated with medical writing
• Continuous self-education in all aspects associated with medical writing
• Managing a team of junior medical writers

Qualifications :

Additional Information :

We prioritize diversity equity and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds genders and ages can contribute and grow.

To succeed we must work together with a human first approach. Why because our people are our greatest strength leading to our continued success on improving the lives of those around us.

We offer :

Our core values are key to how we operate and if you feel they resonate with you then PrimeVigilance could be a great company to join!

Come and join us in this exciting journey to make a positive impact in patients lives. We look forward to welcoming your application.

Remote Work : Yes

Employment Type : Full-time

Key Skills

Clinical Research,Adobe Acrobat,FDA Regulations,Technical Writing,Biotechnology,Clinical Development,Clinical Trials,Microsoft Powerpoint,Research Experience,Document Management Systems,Word Processing,Writing Skills

Experience : years

Vacancy : 1