- 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.
- 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. ...
- Early Phase Development – Project Manager, NBEs - Hertfordshire
My client is an international pharmaceutical company with an acclaimed product portfolio and a stable development pipeline. With a novel R&D wing located in Hertfordshire, the company is in search of an experienced early phase development project manager to oversee the companies' oncology study program.
- Senior Biostatistician (Project Manager)
Senior Biostatistician (Project Manager)An exciting opportunity for a talented biostatistician with strong experience in project management and leading teams of statisticians and programmers for an opportunity with the worlds top global CRO. The role is permanent and can be flexible for home or office based.
- Contract Clinical Project Manager - 12 Months
Contract Clinical Project Manager - 12 MonthsContract Clinical Project Manager required for 12 month contract with global Biopharmaceutical Company. This is an office-based role with International (European) Clinical Study Management and Vendor Management responsibility. ...