Latest Executive Jobs 60

My Client, a growing Biotech is searching for a PVG Manager, to act as the Head of Drug Safety

Acting as the QP you will oversee the PVG Systems set up, and act as the point of contact for authorities. You will also be liaising with the RA and Clinical team heavily, acting as the medical representative for the company.

Our client a Leading Pharmaceutical Company reqiures a Regulatory Affairs Manager to:
• Support the Global Regulatory Leader in representing the function on cross-functional teams (Lifecycle Team).
• Manage the EU registration procedures in EU (Centralised or Mutual Recognition).
• Give specific guidance to the team on EU regulatory issues such as legislation, guidelines, procedures etc.

As one of the largest pharmaceutical services companies in the world, my client covers a range of services and solutions through its offices in more than 36 countries. They are currently looking for a senior Regulatory Professional who can provide a full range of consulting services from a strategic regulatory standpoint.

A Global Medical Communications Company seeks 2 Scientific Directors to work in their bustling Manhattan office.

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.

As Medical Expert in the Neurology therapy area you will be providing medical scientific input to all activities related to planning, execution and reporting of clinical trials. Also, you will delop trial related documents.

Medical/Scientific Director- Highly successful NJ Med Comms Agency

Fantsatsic chance to work for long-established Medical Communications and Marketing Agency based in Central New Jersey.

At present, applications and invited from MDs, PharmDs, and PhDs experienced in the preparation of educational materials (manuscripts, slide kits, monographs, newsletters).

We are looking for a Lead Clinical Research Associate – Combination Products, for our client based close to Zürich, Switzerland. The client is a leading authority on cardiovascular products and holds a large market share in the very competitive market of Cardiac Rhythm Management.

My client is a Swiss based company looking for somebody to Head up their Clinical Development. You will be responsible for providing overall leadership for the Clinical Research group and developing the strategic direction of the department. Applicants must have experience in the Cardiovascular area at a senior level and an MD qualified candidate would be desirable.

Unique, high level position has become available for a Medical Director for this global ophthalmology portfolio focused on the EMEA regions. Overseeing a team of 14 your role will branch across line management of medical managers, strategy for Europe and globally whilst still maintaining a hands-on approach with medical affairs and criticial KOL’s.

Prestigious, respected Medical Director (medical affairs) with one of the fastest growing pharmaceuticals in the world.

Acting as the UK legal signatory for regulatory, promotional and allied materials, you will be a source of expertise and advise on all medical aspects within Medical Affairs. You will provide strategic input into the development and implementation of International Clinical Development and Marketing Plans (ICDP. In addition, you drive marketing and sales operations, e.g. product strategy, campaign development

Medical Director - (Medical Writing background) - MA

Pharmaceutical consulting company seeks a Medical Director with a strong Medical Writing background to work on-site in their MA office.

A Pharmaceutical Company is looking for an experienced Medical Doctor or medically qualified Pharmacovigilance person who specialises in Pharmacovigilance to fill a new and exciting role.

We are looking for a Lead Clinical Research Associate – Combination Products, for our client based close to Zürich, Switzerland. The client is a leading authority on cardiovascular products and holds a large market share in the very competitive market of Cardiac Rhythm Management.

As 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.