They are looking to onboard a Head of RA, who will be responsible for the challenging task of rebuilding an RA strategy for the Tuttlingen business, whilst also being the acting PRRC and EC-Rep for the wider orthopaedics group, supporting other members of the group from China, Europe and the US with accessing the European market. They are looking for a self-starter with expereince leading a tea...
Read morePosition Responsibilities * Prepare regulatory submissions as required for global approvals for medical devices in vitro diagnostic (IVD) products, including preparation of reports and interaction with regulatory officials as required. * Prepare and submit to notified body Technical Documentation needed to demonstrate compliance with applicable European Regulations. * Prepare regulatory submiss...
Read moreClinical Operations Director – Post Marketing Location: Vienna, Austria – Can also be based in Sweden, the United Kingdom, or France Engagement: Full Time Position Flexibility: Hybrid role, if in Vienna 5 days a month in offices. Can vary to suit your location The Company: A medium sized pharmaceutical company with 3 commercialised products and […]
Read moreDirector of Global Post Marketing Surveillance Location: Vienna, Austria – Can also be based in Sweden, the United Kingdom, or France Engagement: Full Time Position Flexibility: Hybrid role, if in Vienna 5 days a month in offices. Can vary to suit your location The Company: A medium sized pharmaceutical company with 3 commercialised products and […]
Read moreMedical Final Signatory About the Company: My client is an EU Leading Life Sciences Consultancy, with over 400% growth in the last 5 years, and have established themselves as a preferred partner for SME’s, Biotech’s, and Large Pharma alike, meaning plenty of growth opportunities for you should you join. They ensure to offer all employees […]
Read moreJob description Provide clinical and technical support to healthcare and to internal customers, helping address medical inquiries *Composing and maintaining standardized response letters *Perform continual independent review of medical/scientific literature on pharmaceutical products (and versus competitor’s, when applicable) *Critically evaluate medical/scientific literature and provide ...
Read moreAbout the Company: Developing products for rare diseases and unmet medical needs, this company is driven by patient-centricity. They have seen 40% growth over the last year, with one approved product already commercialised and multiple more approaching launch. They prioritise the growth and development of their team members and are committed to helping your career […]
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