Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Pharmiweb.com RSS Feed PharmiWeb Candidate Blog

Pharmiweb.com RSS Feed PharmiWeb Client Blog

Job Details

Clinical Development Project Manager – NEW CONTRACT ROLE

Company: Advanced S&S (Medical / Clinical)
Location: South-East
Reference: TMADV / 191216B
Closing Date: 03 Mar 17
Type: Full Time
Salary (£): On Application
Benefits: On Appplication

Job Summary:

This role is on exclusive assignment to Advanced Search & Selection. Please contact Theo Moore or Matt Greig initially on +44 20 7801 3380 or +44 7918 679 405 (until 9.00 pm CET and Saturday mornings) or send a full CV and contact information to theo@advregulatory.com or matt.greig@advregulatory.com who will support your assessment and onboarding process.

Requirements:

Clinical Development Project Manager 

Location: South-East

My client is one of the largest investors in Europe for bio-pharmaceuticals discovery, research and development, and has a large European footprint in the UK. The company is committed to discovering and developing new medicines where there is a high unmet medical need, and the leadership has organised the company around the core principle of patient centricity, data driven decision-making and innovation.

This company’s vision of patient centricity can be measured later in the development and product lifecycle by their glowing primary research from prescribers, KOLs and patient groups.

We have a requirement for an experienced drug development clinical project manager to:

  • Manage the conduct of all the phases of assigned human pharmacology studies, from initial site selection to final report and archival.
  • Operationally lead and coordinate activities of the study team or provide oversight of these duties performed by the CRO or Partner to execute studies in the required countries to deliver timely and high quality study data.
  • Oversee all study related site management and monitoring activities and level of quality of deliverables.
  • Coordinate IEC/IRB submissions. Prepare or review responses to questions from regulatory authorities, and IECs/IRBs or provide oversight of these duties performed by the Partner.
  • Ensure study quality and adherence to the relevant SOPs, GCP, regulatory guidelines and working practices.

My client is not seeking a therapeutic expert, however Project Managers who have around 5 years or more of clinical development experience, ideally in translational or early phases gained with a CRO and/or  bio-/pharmaceutical company, are invited to apply from anywhere in the EU, Switzerland or accession countries.

___________________________________________________________________________________________

If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or alternatively, to have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
___________________________________________________________________________________________

About Advanced

Advanced Search and Selection - Clinical and Medical Division has been operating since 2004.  We are registered and licensed to recruit in the UK, Switzerland, Mainland Europe and the Americas - we have offices in both the UK and Switzerland. We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory, Clinical and Medical Affairs.

We match professional candidates to the best permanent, contract and interim roles in the market and for more information about our company visit us at www.advregulatory.com.

If you wish to apply for this role please click Apply Now, or send your CV with a covering note to CV@AdvRegulatory.com. Alternatively to have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the UK London office, on +44 (0)20 7801 3380.

Keywords / Key words: Clinical,  Clinical, Clinical Research, Clinical, Clinical jobs, Clinical Development, Project Management, Clinical,  Clinical, Clinical Research, Clinical, Clinical jobs, Clinical Development, Project Management

To Apply : Please send a full CV in confidence to cv@advregulatory.com.

Contact Information:

Address:  Head Office
Head Office Suite 8 Penhurst House 352-356 Battersea Park Road London
SW11 3BY
England
Tel:  +44 (0)20 7801 3388
Website:  Visit Our Web Site

Advertising
Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.