The latest Project Manager jobs - BETA

Leading CRO PAREXEL is looking for an experienced Project Manager to join our team. Excellent opportunities and competetive benefits available.

Our client is an aggressively expanding specialist healthcare advertising agency within a global healthcare communications network. This is a fantastic and rare opportunity for an ambitious, enthusiastic and highly Digital Project Manager to work both on their own initiative and as part of the Creative team.

Our client, a specialist global pharmaceutical company and innovative leader in pharmaceutical and health care research and development, is mainly concerned with development activities. They are seeking a Medical Devices Project Manager for a 6 month contract at their Buckinghamshire site.

Are you an experienced Project Manager with an interest in technology looking for a new challenge? Join our Project Management department and let Phlexglobal assist you in realising your potential!

The opportunity to join a global pharmaceutical service provider company which offers the ideal candidate the chance to work on impressive international trials and fantastic career development.

The opportunity to join a world-leading pharmaceutical company which offers the ideal candidate the chance to work on impressive international trials and fantastic career development.

A much sought after opportunity has arisen for an experienced Project Manager to join a healthcare communications agency based in Richmond. The successful candidate will get the chance to work across a number of accounts across a variety of therapy areas.

Senior Project Manager

Responsible for all operational aspects of 1 or more clinical trial(s) (Phase II through lifecycle management) under the leadership of Clinical Trial Head (CTH). Support all scientific aspects of clinical trial(s) as assigned. Responsible for program level activities as assigned.

The opportunity to join a world well established pharmaceutical company which offers the ideal candidate the chance to work on impressive international trials and fantastic career development.

6 month contract, working for a leading Pharma Company, freelancers considered

Our client, a specialist global pharmaceutical company and innovative leader in pharmaceutical and health care research and development, is mainly concerned with development activities. They are seeking a Medical Affairs Project Manager for their Buckinghamshire site.

Project Manager Medical Affairs – Permanent or Interim – Pharma

Do you have experience of project managing Phase IV studies?

Do you have Devices experience?

Would you like exposure to the commercial side of the business?

Do you enjoy travel?

If you can answer YES to all of the above I would like to hear from you.

A much sought after opportunity has arisen for an experienced Project Manager to join a healthcare communications agency based in Richmond. The successful candidate will get the chance to work across a number of accounts across a variety of therapy areas.

A new and exciting role has just come up with a client based in a convenient Surrey location. The organisation, who are a leading international specialist healthcare company, are looking for a Project Manager on an initial temporary basis to support a trainee Project Manager with a varicose vein product.

A new and exciting opportunity for a Project Manager to join a well-established company looking to develop their first medical device.

Regulatory Affairs Project Manager / Leader - Global Development - Switzerland - Excellent Package

For a confidential discussion call Nikolay on +44(0) 207 255 6665 or e-mail nikolay.dimitrov@secpharma.com

A Senior Clinical Project Manager is required for a Global Pharma Company. The position is 1 year contract role based 100% on-site in London. Perfect role for an experienced contractor or those looking to enter the area.

REGULATORY AFFAIRS MANAGER, PHASES I TO IV & POST MARKETING, BIOPHARMA - BASED IN CAMBRIDGE!!

LEADING INDUSTRY EMPLOYER IN THE UK!!

My client has a new role through company expansion for Regulatory Affairs Manager Project Manager, Under the responsibility of Team Leader of Regulatory Affairs and within the framework of dedicated projects, you will ensure international coordination of development projects to the regulatory portion (EU, United States, Japan and emerging countries).

Project Manager Medical Affairs
Permanent Position, Buckinghamshire

We''re seeking an ambitious leader who enjoys autonomy and the scope arising when working within medical affairs in Late Phase and product lifecycle. In this role you will do a 360 degree role from protocol definition to publication and your remit will include KOL nurture and analysing market strategy in terms of new indications for use, patient populations and markets. This is a EAME regional

Project Manager Medical Affairs
Contract Position, Buckinghamshire

We''re seeking an ambitious leader who enjoys autonomy and the scope arising when working within medical affairs in Late Phase and product lifecycle. In this role you will do a 360 degree role from protocol definition to publication and your remit will include KOL nurture and analysing market strategy in terms of new indications for use, patient populations and markets. This is a EAME regional r

Biotechnology project management role. Full span of development from bench to licensing. Global role, based in Berks, UK.

Introduction
Do you have a strong project management background in the development of vaccines or other biological products? Do you have formal project management expertise such as PMP or Six sigma certification? Do you have experience of taking a product through BLA or NDA submissions? If so, our client, has an permanent role that your skills could match.

An outstanding opportunity to join one of the world’s leading contract research organizations and be part of a dynamic and growing international company. Join PRA as a Project Manager and help realise your career potential

My client – one of the top five Contract Research Organisations ( CRO ) – is looking for a Project Manager (PM ) and a Senior Project Manager ( Senior PM / SPM ) to join their established, dynamic, high-calibre team. The company has recently won a series of new clinical trials with some of the largest blue-chip companies in the field and is now looking to expand their team.

My client – a top contract research organisations ( CRO ) – is looking for a Project Manager (PM ) to join their established, dynamic, high-calibre team.

Mid-sized CRO require Senior Project Manager (Senior PM ) to join a well established and forward thinking team / organisation - permanent Senior PM position - home based UK wide

Mid-sized CRO require Project Manager ( PM ) to join a well established and forward thinking team / organisation - permanent Project Manager ( PM ) position - home based UK wide

Rare opportunity to join a world class pharma company as junior project manager ( junior PM ) in a 12 month rolling contract - full time - office based position located in West London.

As a key member on project teams the GPM is expected to actively contribute and challenge the definition and development of project strategy, and then help teams to effectively and efficiently deliver on the strategic objectives agreed with the relevant governance body. The GPM partners with the team leader to anticipate, identify, manage and communicate project risks. GPMs achieve this by delivering high quality project management support and other high value services.

Manage and co-ordinate all technical and service aspects of an Interactive Response Technology project used for randomization, supplies management, and forecasting for clinical trials. This will range from initial discussions with clients, development of the project specifications, documentation aspects of setting up the project and management of all project related activities through to study completion.

Did you know…that of the world’s top 30 best-selling drugs, Quintiles helped develop or commercialise every one?

Project Lead/Project Manager (Late phase studies) Germany. Office based in Berlin | Frankfurt | Munich My client is a leading global biopharmaceutical services organisation and are currently seeking an experienced Project Manager to lead and manage domestic and international late phase studies. With more than 10,000 employees worldwide, my client operates 71 locations throughout 54 countries and have worked with all 10 of the world's top 10 pharmaceutical companies.

Regulatory Affairs Project Manager Location: Berkshire Employment term: Permanent Salary: £55,000-£60,000 An exciting opportunity has arisen within a global pharmaceutical company, located in Berkshire as a Regulatory Affairs Project Manager. The Project Manager will provide regulatory advice and support to the UK company affiliate.

To apply for this regulatory affairs project manager please call Julie Cooper on 0208 305 9733 or 07951 082482 Alternatively please send your CV to: julie@mosaicrecruitment.co.uk

Regulatory Affairs CMC Project Manager Location: Northern Spain Employment type: 6 month Fixed Term Contract Salary: £35,000 per 6 months. An expanding biopharmaceutical company in Northern Spain is currently recruiting for an experienced Regulatory Affairs CMC Project Manager, with hands-on knowledge of the European regulatory framework within the CMC section for biologics.

Medical Affairs Project Manager, Permanent position

Regulatory Project Manager, Cambridgeshire/ Hertfordshire (UK)

A leading biopharmaceutical company which is a growing year on year is searching for a Regulatory Project Manager to co-ordinate, prioritise and track regulatory activities. This exciting opportunity will mean the successful candidate will oversee several established and professional teams in both early and late stage product development and marketed products.

ClinTec International are recruiting on behalf of a global research organisation who provide; analytical instruments, laboratory supply chain programs, eCommerce and laboratory equipment.

SENIOR PROJECT MANAGERS NEEDED IN - SPAIN / PORTUGAL / FRANCE / GERMANY. For a full job specification and to discuss this great client please call me on 00 44 1142 096320 or email me amoran@acr-uk.com and I can arrange a call at a convenient time for yourself.

To apply for this regulatory affairs project manager please call Julie Cooper on 0208 305 9733 or 07951 082482 Alternatively please send your CV to: julie@mosaicrecruitment.co.uk

For over 30 years PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, we supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries

Our client is currently looking to recruit an IT Project Manager for a contract role.

Well established Pharma company is looking for experienced Project Manager.

Our client, a leading global CRO, provides a comprehensive range of services in Phase I-IV clinical trials to the biopharmaceutical and device industries. They are currently seeking an IT Project Manager for a 12 month contract at their Dublin site.

A new and exciting role has just come up with a client based in a convenient Surrey location. The organisation, who are a leading international specialist healthcare company, are looking for a Project Manager on an initial temporary basis to support a trainee Project Manager with a varicose vein product.

This is a full time PERMANENT position based at our office in Bad Homburg. Home based CRAs will also be considered. You will have the ability to work independently and as a part of a team

An outstanding opportunity to join one of the world’s leading Clinical Research Organisations and be part of a dynamic and growing international company. Join PRA as a Manager of Project Administration based at our Reading office, and help realise your career potential.

Project Manager with potential and desire to succeed further in clinical world is required for successful Global CRO

Titel: Global Regulatory Affairs Project Manager (m/f)
Location: Thuringia, Germany
Permanent position

Phlexglobal are looking to recruit a number of experienced Project/Study Managers for an exciting new eTMF project!

Our sustained year on year growth at PPD means that we are looking for Senior level Project Managers based in UK, Belgium, Germany, Spain, Poland, Italy and France to join our rapidly growing teams.

We are assisting our CRO client in finding a Senior Project Manager to manage their clinical trials.

Our client, a Dublin based pharmaceutical manufacturing company, currently has a vacancy for a Manufacturing Project Manager.

A freelance Senior CRA / Junior Project Manager with 3+ years Clinical experience is required by a rapidly expanding Drug Development Services Company based in Cambridge. Projects are ongoing in a range of therapy areas, and the freelancer is required for an initial six month contract with the possibility of extension. This is predominantly an office based role in Cambridgeshire, with some flexibility to work home based part time. This is a full time contract.

My client – one of the top five Contract Research Organisations ( CRO ) – is looking for a Project Manager (PM ) and a Senior Project Manager ( Senior PM / SPM ) to join their established, dynamic, high-calibre team. The company has recently won a series of new clinical trials with some of the largest blue-chip companies in the field and is now looking to expand their team.

***OPTION SUISSE*** International RA Development Project Manager - Join one of the largest & forward thinking companies in the industry! Advanced is retained on this mission and welcomes your application. Please contact Marc Van de Voorde on +41-41-710.51.00 or alternatively send your CV to cv@advregulatory.com

An outstanding opportunity to join one of the world’s leading contract research organizations and be part of a dynamic and growing international company. Join PRA as a Project Manager and help realise your career potential

A Clinical Associate Director/Senior Manager is required to join a leading pharmaceutical company!

You will be acting as Regulatory Affairs Project Manager for a successful pharmaceutical company in Basel.

Medical communication agency in the Oxford area has an excellent opportunity for a creative and experienced Digital Project Manager to join their growing team and take responsibility for delivering project management services and high quality digital projects to meet clients’ needs.

Please consider this role! To respond, for French and German speaking candidates should apply to Marc Van de Voorde in our Swiss office, Marc@Advregulatory.com or on +41 (0)78 170 4042 and for candidates from the UK, NL and rest of world to Matt Greig, in the UK London office, to Matt@Advregulatory.com or call +44 (0)7918 679 405.

Senior Project Manager - Medical Communications Berkshire £45k The Company: Our Client has five offices serving the United Kingdom covering a range of clinical and commercial services. Since opening their offices 25 years ago they have consistently delivered innovative solutions to pharmaceutical companies across the country and the globe. The Position: They are now seeking a Senior Project Manager

A major Belgium based pharmaceutical company are seeking a regulatory affairs professional with 3 to 7 years pharmaceutical experience with knowledge of regional regulatory procedures and legislation related to lead one of the following projects: drug development, product registration, line extension or license maintenance. This role comes with excellent training and real career development opportunities … Contact Theo Moore or Matt Greig on +44 207 801 3380

My International pharmaceutical client is looking for a talented regulatory affairs Associate Director to provide strategic & operational support to Global & regional based project teams for both development & Life-cycle management projects. You will also have at least 10 years experience of hands on European regulatory activities in a matrix environment. Contact Theo Moore or Matt Greig on +44 (0) 207 801 3380 or email cv@advregulatory.com to apply for this position.

Please call me, Matt Greig on +44 (0)207 801 3382 or direct on +44 (0)7918 679 405 (eves / weekends). Alternatively you can email me on Matt.Greig@AdvRegulatory.com

Please call me, Matt Greig on +44 (0)207 801 3382 or direct on +44 (0)7918 679 405 (eves / weekends). Alternatively you can email me on Matt.Greig@AdvRegulatory.com

I am a senior recruiter within the industry across a number of job divisions for the pharma, biotech and CRO sectors. For a confidential and professional chat about your requirements/ career advice and the chance to register for free and receive weekly job updates, please call Alex on 01206 848439 or email alex@apexrecruitment.com

A global Medical Communications Agency is looking for Project Managers with demonstratable experience of medical education delivery in the pharmaceutical sector, either client or agency side.

A global giant in medical devices is looking to add to their existing team in the North West of England, this exciting company operate in various fields but have a significant market share in the orthopaedic device sector, where this role is based. With an aggressive plan for 2012 this organisation are looking for the best of the best to join their Regulatory team to cover an extended maternity period.

An outstanding opportunity to join one of the worlds leading contract research organisations and be part of a dynamic and growing international company. Join PRA as a Project Director or Senior Project Manager, and help realise your career potential.

INTERIM PROJECT MANAGER - MEDICAL AFFAIRS (BASED IN: BUCKINGHAMSHIRE) (SALARY: ON APPLICATION) We are seeking candidates with a genuine passion, who like to work at an exceptionally fast pace, and can work autonomously.

Opportunity for an experienced Regulatory Affairs Project Manager to join this well known and successful Pharmaceutical company. The role is offered on a permanent basis and can be based at either of the company’s sites, Hampshire or Berkshire. You will need experience of the UK market (MHRA), MRP / DCP and Variations and be happy deputizing for Senior colleagues.

A leading Healthcare Communications Agency is seeking a Digital Project Manager

I am a senior recruiter within the industry across a number of job divisions for the pharma, biotech and CRO sectors. For a confidential and professional chat about your requirements/ career advice and the chance to register for free and receive weekly job updates, please call Alex on 01206 848439 or email alex@apexrecruitment.com

If you're looking for a high-performing, high-rewarding opportunity and want to showcase your charismatic skills in a culture that embodies real results within regulatory affairs then this could be the company and role for you. Real EU and global development roles available. Excellent career opportunities available. Contact Theo Moore or Matt Greig on +44 207 801 3380

This is a fantastic position within a growing organisation. To ensure the smooth running of major projects within the Pharmaceutical & Pharmacy sector.

Please call me, Matt Greig on +44 (0)207 801 3382 or direct on +44 (0)7918 679 405 (eves / weekends). Alternatively you can email me on Matt.Greig@AdvRegulatory.com

Key People are recruting for an IVRS Project Manager for our global pharmaceutical client based in Switzerland

Our client, a leading global clinical research organization, currently has a vacancy for a Manager, Project Management

Ensures the contracted services and expectations of a clinical study are carried out by the INC Research (INCR) project team in accordance to the executed contract and the Customer’s expectations

Ensures the contracted services and expectations of a clinical study are carried out by the INC Research (INCR) project team in accordance to the executed contract and the Customer’s expectations.

OPTION SUISSE * * * Emerging Markets Project Manager * * * Beat the downturn, low tax rate and high salaries plus relocation A true giant in the pharmaceutical sector, now seeking individuals who want to lead the registration of high value compounds in the major market areas, Brazil, Russia, India, China, Korea and other ... (see text) Please call Matt Greig on +44 (0)207 801 3382 or direct on +44 (0)7918 679 405 (eves / weekends). Alternatively you can email me on Matt@AdvRegulatory.com

Just Pharma are assisting in the search for a Project Managers to be office based in London.

Our client a leading web based clinical technology company now have a vacancy for a Project Manager. The company is in an active growth stage during the market roll out of its innovative products This

Senior Project Manager / Senior PM / SPM An exciting opportunity for experienced Project Managers ( PM ) to join a fast-growing mid-size global pharmaceutical organizations and become a Senior Project Manager ( Senior PM ) in their offices in Moscow. Permanent , full time , office or home based .

Lead and provide regulatory strategy to submit scientific advice, achieve the successful application of a PIP and submit and validate an EU centralised MAA. Contact Theo Moore on +44 207 801 3380 or email me in confidence on cv@advregulatory.com

Please call Matt Greig on +44 (0)207 801 3382 or direct on +44 (0)7918 679 405 (eves / weekends). Alternatively you can email me on Matt.Greig@AdvRegulatory.com

A dynamic and well known Pharmaceutical company is looking for talented professionals to join their Regulatory team responsible for all countries in Europe, the Middle East and Africa (EMEA). Contact Theo Moore or Matt Greig on +44 208 801 3384 or email theo@advregulatory.com to discuss this role further

OPTION SUISSE *** O N C O L O G Y *** Early and Late Stage Regulatory Development Project Manager * Relocation, great salaries, low tax! In the first instance, please contact Matt Greig or Theo Moore on +44 (0)207 801 3380 or out of hours you may call +44 (0)7918 679 405, alternatively, send a full CV today in confidence to matt@advregulatory.com

*** Option Swiss*** Life Cycle Management role*** Regulatory Project Manager*** Global PharmaCo ***Location : Europe, Switzerland,If you wish to apply for this role please click below, or send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options call Theo Moore on +44 (0)207 801 3384 or +44 (0) 791 819 5166.

As Regulatory Affairs manager for a small team that is set to grow you will set out strategy, direct and contribute to the planning, preparation, review and submission of high quality applications to regulatory authorities leading to approval in a timely manner (in a role which is varied, dynamic, evolving and highly strategic). Contact Theo Moore on +44 (0)207 801 3384

Just Pharma are assisting in the search for Junior Project Managers to be office based in London, Madrid, Frankfurt, Berlin, Warsaw, Milan or Bucharest.

Please call Matt Greig on +44 (0)207 801 3382 or direct on +44 (0)7918 679 405 (eves / weekends). Alternatively you can email me on Matt.Greig@AdvRegulatory.com

This is a role for those who really want to learn all there is to know about Regulatory affairs development in the biological sector…!!! My client is looking for a Regulatory professional with over 5 years experience for a regulatory strategy role for Biological/biotech development projects. This is role that covers project management from Phase 1 through to P3 and onto Centralised submissions. Contact Theo Moore on +44 207 801 3384 or email me at cv@advregulatory.com

My client is a leading global health care company We are a global, broad-based health care company devoted to discovering new medicines, new technologies and new ways to manage health. They are looking for an experience individual to join growing team as the Regulatory Affairs Project Manager.

Please call Matt Greig on +44 (0)207 801 3382 or direct on +44 (0)7918 679 405 (eves / weekends). Alternatively you can email me on Matt.Greig@AdvRegulatory.com

Please call Matt Greig on +44 (0)207 801 3382 or direct on +44 (0)7918 679 405 (eves / weekends). Alternatively you can email me on Matt.Greig@AdvRegulatory.com

We are assisting our CRO client in finding a Senior Manager/Director, Project Management to manage and lead the Technology Project Management Team and represent the Technology division with external and internal clients. The successful candidate will lead release planning to ensure Technology releases meet timeline and customer expectations. The position is based in West Sussex.

My client is looking for a Project Manager to join their hugely successful global team in the UK.

My client is looking for an experienced Project Manager to join their hugely successful Global Team.

Our client is a top medcomms agency formed of experienced digital experts within the healthcare industry, helping clients to navigate the world their customers live in and interact with them in the most meaningful and impactful way.

A Global Medical Communications Agency in central London needs a dynamic Project Manager. To £55k

Develop and execute European regulatory strategies for Biological and NCE development projects. Take European responsibility for managing both development products and marketed products, across one of 8 therapy areas including activities on licensed biological compounds and NCEs in development. Contact Theo Moore or Matt Greig on +44 208 801 3384 or email theo@advregulatory.com to discuss this role further

Forward thinking client which is rated in the Top 10 of world Pharmaceutical companies - Excellent Benefits package which includes a great salary & benefits package - Strong pipeline with Oncology, CNS, Pain, Inflammation and Cardiovascular products in late phases of development - Location: Switzerland, Basel, Neuchâtel, Geneva, In the first instance please call Matt or Theo on +44(0)207 801 3384 or +44 (0) 7918 195 166 or please send a full CV to Theo@advregulatory.com

My client is a global provider of Health Economics Outcomes Research, Epidemiology, Pricing & Reimbursement and Market Access service to the Pharmaceutical industry. They are looking for an Epidemiologist Project Manager for their UK offices.

Chiltern is looking to recruit an experience Global Clinical Project Manager that has had some exposure to Oncology projects.

Snr Regulatory Project Management role for a company which boasts a rich pipeline of products in development for oncology, central nervous system, infectious diseases, virology, cardiovascular disorders, inflammatory and autoimmune diseases. Location: Switzerland, Basel, Neuchatel, Geneva, Allschwil.

Join an organisation that has excellent training and development opportunities and interesting and commercially focused EU regulatory projects. The product range is varied and the scope for developing your experience and expertise is excellent. Alternatively to have a confidential discussion about this or other potential roles or career options call Theo Moore or Matt Greig on +44 0207 801 3384

Key People are recruiting for a Senior Project Manager for our large global pharmaceutical client

***Regulatory Affairs EU Project Manager***Switzerland***Use your CTA to Gain FULL CP Exp***Great salary & package***Top Ten Pharma still expanding* In the first instance please call Theo Moore on +44(0)207 801 3384 or +44 (0) 7918 195 166 or please send a full CV to Theo@advregulatory.com

This global Medical Education agency are looking for a proven project manager with several years experience of medical education delivery in the pharmaceutical sector, either client or agency side.

Global Medical Education agency are currently looking for a proven project manager with several years experience of medical education delivery in the pharmaceutical sector, either client or agency side.

Join a Top Ten Pharmaceutical company in a Global role. Take the Lead on major indications for Pharma or Biotech compounds. Operate from a Global Head office. FULL RELOCATION, Very good Salary, strong package, very low tax and a bonus. Contact Theo Moore on +44 (0) 207 801 3384 or e-mail theo@advregulatory.com

Regulatory Affairs Manager – Biotech Role for a Blue-Chip Pharma / Switzerland

This role will give you full hands on Centralised procedure submissions experience then allow you to move into a global role. This really is an excellent opportunity to develop your expertise in a friendly & commercially focused environment for one of the worlds fastest growing Pharma companies.

Join an expanding Pharma company which offers you excellent career opportunities and Global project work for Pharma and Biotech projects – Excellent training available. Location: Geneva/ Lausanne – Contact Theo Moore +44 207 801 3384 or email your Cv (in confidence) to CV@advregulatory.com to apply for this role.

This is a very unique opportunity for a talented Country Project Manager to join this terrific global client of ours. The position is to be based out of Spain.

Just Pharma are currently looking for a project managers and project leaders for a vacancies through out Europe. Opportunties also for Senior Project Managers and Leaders.

Just Pharma are looking for an experienced project manager for a global full service position.

Just Pharma are currently looking for experienced project managers for a number of project manager vacancy within large companies in the pharmaceutical industry, office or home based through out Europe.

Location: Basel - Join a leading Pharmaceutical company in a role that covers EU and Global projects. Therapeutic areas are varied and includes oncology, CNS, Immunology. You will also be working on small molecule and Biotech projects. Contact Theo Moore on+44 (0)207 801 3384 or email me at Cv@advregulatory.com

OPTION SUISSE *** O N C O L O G Y *** Early and Late Stage Regulatory Development Project Manager * Relocation, great salaries, low tax! In the first instance, please contact Matt Greig or Theo Moore on +44 (0)207 801 3380 or out of hours you may call +44 (0)7918 679 405, alternatively, send a full CV today in confidence to matt@advregulatory.com

Please call Matt Greig on +44 (0)207 801 3382 or direct on +44 (0)7918 679 405 (eves / weekends). Alternatively you can email me on Matt@AdvRegulatory.com

Just Pharma are currently looking for experienced project leaders and managers for office and home based Project Managers and Senior Project Managers.

Utilise your CMC experience in a role which will cover all aspects of drug development, product registration and lifecycle management for major European Markets. Join an RA Department which is widely regarding as one of the strongest CMC teams in the EU. Project work is varied and broad-based, with lots of variety and scope. Contact Theo Moore 0n +44 207 801 3384 or email your Cv in confidence to Theo@advregulatory.com

Global Project Manager or Senior Global Project Manager position within leading CRO - Office based in M4 area or fully home-based - Great Salary

Superb opportunity for a Project Manager / Clinical Trial Manager to join a world class Biotech and specialise in Patient Recruitment and Feasibility.

Contract Junior Project Manager / Junior Study Manager position in leading Biotech company with unrivalled career progression and development based in the West London area.

Contract Junior Project Manager / Study Manager position in leading Biotech company based in the Cambridgeshire area.