- Senior Project Manager - Medical Affairs Research Operations-123777
Background to the position:
The market of peri- and post approval studies is expected to significantly grow in the future. In response to the growing market of late phase studies PPD is committed to enhance its late phase capabilities in Europe and expand its Late Phase Department in Europe. In the context of this departmental expansion PPD is attempting to hire an individual with the right mix of skills and experience. ...
- Regulatory Affairs Project Manager - BIOTECH
My Cient (biotech company) is the world leader in the the development of controlled substances for medicinal use.
There is currently a vacancy within medical affairs for a regulatory project manager who will specialise in overseeing the regulatory aspects for the companies flaghsip product - a controlled substance used (and currently licensed in many countries) to treat MS, with on going studies in cancer pain and paediatric epilepsy.
- Product Launch Project Manager - Prague Czech Republic
Product Launch Project Manager required by leading Medical Device Company in Prague, Czech Republic. Excellent conditions and opportunity to develop the career on offer.
- Regulatory Affairs Manager \ Regulatory Affairs Project Manager \ Regulatory Submissions
Regulatory Affairs Manager \ Regulatory Affairs Project Manager \ Regulatory Submissions
Our client is a leading global contract research organisation providing drug discovery, development and lifecycle management services. Their clients and partners include pharmaceutical, biotechnology, medical device, academic and government organisations.
- PW 6158 Client Project Manager
Exciting opportunity for a project manager to join this niche and energetic organisation. You’ll manage projects from inception to conclusion and client relations ensuring the delivery of an exceptional service, on time and to budget. Building strong, lasting client relationships and securing further ongoing projects/ work opportunities for a specific service within industry.
- Quality Assurance and Regulatory Affairs Manager – Small medical device firm – UK
An opportunity has arisen for an experienced QA manager to join my client, a small medical device firm and be based at their UK site. The company, who operate as a subsidiary of a much smaller company are looking for an individual with a thorough understand of all medical device regulations to lead their small team and aid in the company’s development.
- PW 6335 Global Submission Specialist / Regulatory Submissions Project Manager
Opportunity for a Submissions Manager to join this Top 20 Pharma on a fixed term contract as our Client’s Global Regulatory Submissions Specialist. The role is office based in the South East, focuses on compliant submissions, Ectd standardisation and sits within a cross functional global team. Contract length is 6 months and strong likelihood to extend further.
- Clinical Project Manager – Early Phase R&D, Oncology
JOB TITLEClinical Project Manager – Early Phase R&D, OncologyROLE DESCRIPTIONThis is a rare opportunity for a Clinical Project Manager. Someone who is innovative by nature and who wants to be a part of an exciting arm of one of the world’s leading Pharmaceutical companies.As Clinical Project Manager – Early Phase, you will be driving the development of ground-breaking products through Phase I & II studies or programs of oncology studies. ...
- PW 6158C Account/ Client Project Manager
An exciting opportunity for an experienced project manager to join this niche and energetic organisation. The ideal candidate will have an industry background working within either a pharmaceutical or clinical research environment. You will manage client projects with a clinical focus from inception to completion ensuring delivery of an exceptional service to industry leaders.
- Clinical Project Manager - Freelance - Home based
Experienced FREELANCE CLINICAL PROJECT MANAGER is required by a global contract research organisation for a 12 month contract to provide strategic leadership of international clinical trials. As a full service Clinical Project Manager, you will have proven success in leading cross functional project teams to deliver complex Phase II-IV studies. ...