Latest Executive Jobs 55

As Medical Director you will be responsible for ensuring the accuracy of all scientific
and medical content and staying abreast of current advances in your speific therapeutic area

You will provide guidance to internal writers and mentor them in the writing of the medical content. You will interact with clients to provide strategic direction andrecommendations for execution of their projects.

OPTION SUISSE * * * GLOBAL Regulatory Affairs Director *** Beat the downturn, low tax rate and high salaries plus relocation A true giant in the pharmaceutical sector with a global matrix managed by this function, Global Regulatory Directors, leading strategy to file, and major product, major lifecycle ... SEE TEXT Please call Matt Greig or Theo Moore on +44 (0)207 697 7300 or please send a full CV to CV@advregulatory.com

You will coordinate and conduct PV specific audits of internal systems and external service providers/business partners, develop specific audit plans, leads, and independently performs complex PV compliance audits and provides expert guidance for resolution of audit findings; and prepare documentation of audit observations and provide guidance for the development and completion of risk mitigation strategies

My Client is looking for an MD with 10 years in the industry and excellent experience in pulmonary vascular disease. This is a unique opportunity with an excellent salary and career progression on offer.

Senior Manager, Pricing & Market Access, Switzerland, Upto 180k (chf)

Leading Biotech in PA is seeking a Senior Scientific/Regulatory Writer to work as one of their medical writing experts, responsible for the research, writing, and editing of regulatory documents. You will provide full lifecycle support from clinical study protocols through abstract/manuscript preparation and submission, and sales tools.

A European Leadership role is available with rapidly growing and dynamic product innovator who are leaders in their field. This company has developed an innovative technology platform which is a world first. They already have one marketed product which has an outstanding potential for new indications and their development pipeline – primarily within oncology – is strong. Based in the UK, you will be a key figure in the development and growth of this young company.

Interim Regulatory Affairs Associate
3 to 4 week contract £250 to £300 per day.

An Ideal opportunity to work with a global healthcare company as an Interim Regulatory Affairs Associate. Working on preparation for submission of variation

My client, a Pharmaceutical, has an opportunity for an expert in PVG for a Head of Drug Safety

You will be overseeing the medical and safety aspects on assigned own, and on drugs of team members of own Unit. You will also supervise and lead a scientific approach of assigned PVLs in analysis and management of potential risks related to the assigned drugs.

My client, a Pharmaceutical specialising in the Meta, Diabetes and Oncology therapeutic areas, has an opportunity for a Medical Advisor in the Diabetes indication
You will be providing medical expertise in the area of Diabetes. This will include providing strategic medical input into the marketing plan for products in late phase development, review and approve Phase 4 Studies, and interacting closely with RA and PVG Departments with regards to product strategies

As a Statistical Programmer you will be expected to:

* Provide input as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial level activities.

Health Economics Manager/ Europe /HE&0R/Outstanding place to work, Location: Switzerland Please call Nikolaus Greig for this role or any other positions in Health Economics, Pricing / Reimbursements, OR & Market Access on +44 (0) 207 697 7300 - alternatively please email he@advregulatory.com

This is a global HE management position for a well-known pharma, based in Switzerland.

Opportunity to join a leading Medical Communications Agency, part of a Global Contract Research Organisation. Key and senior hire within in the business, working alongside the Global Head. You will resume responsibility for business management and strategy, financial management, project delivery and team management.

My client is a Biopharmaceutical company focused on the development of therapeutics for conditions related to the vascular system, has an opportunity for a Head of Drug Safety to act as the QP for PVG. This is a new position in a rapidly growing company.