Company: RBW Consulting
Closing Date: 24 Mar 17
Salary (£): Competitive
We are now looking for an experienced Medic to join my clients international Medical Affairs team in Sweden. This role will be working globally in a team of about 20+ colleagues. You will as a Sr Medaical Advisor be working cross-functionally with the departments of marketing, regulatory, clinical development etc.
We are now looking for an experienced Medic to join my clients international Medical Affairs team in Sweden.
This role will be working globally in a team of about 20+ members. You will as a Sr Medaical Advisor be working cross- functionally with the departments of marketing, regulatory, clinical development etc.
About the job
As a key responsible medic in the team you will be focusing on leading and overseeing the amalyses, interpretations and presentation of the clinical data as well as working together with the rest of the team to conduct phase 4 studies and perform more medic related tasks in clinics as well. Therefore the role will require you have a medic degree and have experience of working in a clinic prior to Medical Affairs experience.
Act as physician for the organisations phase 4 studies
Reviewing and approving responses to regulatory authorities and agencies pertaining to medical and scientific data
Reviewing and approving the claims sheet for marketed company products in the aesthetic and corrective portfolio
Act as the medical lead for publication planning in conjunction with colleagues in the Scientific Division, Preclinical group, and Medical Affairs
Ensuring that all study and publication activities conducted by the company’s Medical Affairs team reflect the input and knowledge of external experts, current clinical practice worldwide, internal company data, and the published literature
You are a physician and have practiced clinical medicine or a medical or surgical specialty for a minimum of 5 years
You have work experience for a minimum of 3 years in a global pharmaceutical and/or medical device company in Medical Affairs
You possess excellent communication skills in English, both verbal and written
You have the ability to manage multiple projects and requests while maintaining timelines and able to meet expectations of others for high quality deliverables
You have proven ability to work cross-functionally and build relations among stakeholders
Knowledge of international regulations and GCP of pharmaceuticals
Experience in conducting phase 4 studies; experience in Medical Affairs study strategy and planning of merit
You have experience in critically reviewing and analysing scientific data, and have demonstrated ability to outline and write scientific papers and compile regulatory and technical documents
You have experience compiling documents, medical publications and reports that meet regulatory standards and guidelines
Southdown House, 130a Western Road, Brighton BN1 2LA
|Tel:||01293 584 300|
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