TRABAJO MANAGER REGULATORY SUBMISSIONS MEDICAL

•    finalize and review regulatory documents and submissions...   the manager regulatory affairs is responsible for regulatory leadership in project teams by providing...

Spotlab is transforming the healthcare medical diagnosis industry... experience in the registration and post-market surveillance of in vitro diagnostic medical devices...

Acting as lead medical writer, on projects with multiple deliverables/components... • you may act as project manager for a small series of medical writing projects...

Review and approve data and documentation required for medical device/pharmaceutical combination product regulatory submissions... review medical (information) and...

Application of medical technical expertise and keen insight will increase the scientific impact of gsk’s ch business activities...   this role collaborates extensively...

Assists with regulatory intelligence by monitoring the global regulatory environment and providing regulatory summaries and dissemination of critical materials...

As a manager/senior manager in the medical writing group responsibilities include management of the day to day activities of the mw team... that’s our vision...

• experience in medicinal product and medical device regulatory affairs... • ensures training for the regulatory affairs staff... • develops budgets for the regulatory...

To provide strategic regulatory guidance and information to projects; to acquire pertinent regulatory information from agencies and organizations; to support regulatory...

Global responsibility the manager, global regulatory affairs is responsible for defining and implementing global roll out regulatory strategies including regional...

Lead the process for filing regulatory submissions... develop procedures to ensure regulatory compliance... assure regulatory compliance and interpretation of regulatory...

regulatory project manager –immuno & inflammation about the job our team join sanofi global regulatory affairs team as regulatory project manager – immuno &...

·        extensive regulatory medical writing experience that is usually demonstrated by 7 years or more experience within a cro or pharma organisation...                                                      ...

Arranges meetings for regulatory part within project teams or regulatory agency... conducts initial review of regulatory agency publications... key accountabilities/responsibilities:...

Must have medical devices and medical device technology experience... 2+ years working in the medical industry... experience working within a qms medical directive...

Ensuring regulatory compliance in the applicable market(s) as part of the iqvia global regulatory affairs department, you will be working with our clients – global...

To accomplish this, the manager medical writer liaises primarily with the director medical writing, and in collaboration with internal and external stakeholders...

Verify electronic publishing of regulatory submissions... act as regulatory representative at meetings with business partners and regulatory agencies...