The latest Project Manager jobs - BETA

Our client is currently seeking a Patient Recruitment Project Manager. This post will be based within their London office and will mark a key hire for this company.

Senior Project Manager Pharmaceutical Development- Switzerland

A global pharmaceutical company are seeking a highly experienced project manager with strong experience in drug discovery to lead all technical development activities for assigned compounds (small molecules).

Role My client is an innovative company with business dimensions in generic and branded products. They are seeking a Manager, Global Project Management to work on a permanent basis from their offices in Frankfurt.

The Project Data Manager (PDM) is responsible for the data management aspects of one or more clinical studies or project. These studies would be like 3 to 4 Phase 2a studies plus 3 Phase I studies.. The PDM will be responsible for the effective communication within the corporation and, where appropriate, with external organisations of the issues and actions related to the successful completion of data management activities within the project(s).

Artwork Project Manager - Contract - Berkshire Shreeya Patel is recruiting for an Artwork Project Manager to join a global pharmaceutical company at their site...

Reporting to the Senior Manager, Manufacturing & Logistics you will be an integral member of a commercial operations team in basically a planning role managing the delivery of multiple interrelated projects to ensure the reliable supply & quality of pharmaceutical products throughout Europe. This is a newly role created position to create a culture of project management and to support Project Leaders with the delivery of Business & Marketing Dept projects.

I am currently looking for the best candidates to fill a Senior Project Manager Study Start Up role. This is an exciting opportunity for candidates to project manage and lead core project teams during the Study Start Up phase of clinical trials. This role will be a home based role and candidates will be considered in locations all over Eastern Europe.

The responsibilities of the position will include conducting clinical trials in Germany, Austria and Switzerland, supervision and coordination of participating CROs and partner companies, contact and close communication with the Company Headquarters, worldwide internal and external research centers, medical and clinical experts and relevant authorities, attendance of international expert meetings within the study implementation and leading of a clinical team for studies in Oncology and CNS.

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 Swansea office, and help realize your career potential.

One of the leading research organisation is looking for an experienced Project Manager.

One of the leading CRO is looking for an experienced Project Manager.

I am currently recruiting for a specialist company, undertaking late phase consultancy services to the pharmaceutical industry.

Be the key expert within a leading company that specialize in both medical devices and pharmaceutical products. As the Regulatory Affairs Manager, you will be part of the global market that this company has widespread presence in. In this specific role you will be project managing and leading the registration process within the APAC region. Leading to an interesting and varied working life, due to the changing regulations.

**Project Manager Study Start-Up** EASTERN EUROPE My Client are currently seeing a big growth in their study start-up team and are looking for a number of new colleagues all over Europe with focus on Russia. In this role you will have a great opportunity to progress in your career and develop. This is an exciting opportunity to project manage and lead the project team during study start-up phase

We are actively seeking an experienced Project Manager from a CRO background to join our team based in Belgium to manage clinical trials stages I through IV

My client, a small CRO, is currently seeking a Junior Project Manager to work in Oncology on an initial 6 month contract You will be working on site set up, contract negotiation, budget etc.

This role would be suitable for applicants with the following experience: Project manager, Product Manager, Supply chain manager, Junior Supply chain manager, Drug delivery Manager, Drug development Manager

Scientific Recruitment and Retention Project Manager. My client, an innovative and forward thinking global pharmaceutical company, who are committed to producing finest in class products, are offering an excellent opportunity to join them as a Scientific Recruitment and Retention Project Manager. Office based in the South East of England

Study Start-Up Manager: This is a great opportunity for an experienced regulatory and start up specialist to move into a Start Up Project Manager role. Working for a top 25 international CRO with big growth plans for the next couple of years will offer you plenty in the way of career progression and personal and professional development. Ideal for a CRA/PM/Start Up specialist looking for a change.

A small but fast growing niche early-phase CRO are currently recruiting for a permanent Project Manager position. This is a great opportunity for an...

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

You will manage the technical transfer of Bulk oil manufacturing (including some APIs)

Key Accountabilities:

* Develops and manages the project plan to support the transfer of bulk oil manufacturing
* Coordinates the project activities between Regulatory, Quality and Technical to agreed timelines.
* Develops a risk assessment for the project and ensures all risks are managed and mitigated where necessary. ...

inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bioanalytical services, and strategic resourcing from a single clinical professional to an entire functional team. ...

My client is a medium-sized CRO. They work together with a range of highly reputed partner sponsors across Germany and internationally.

A fantastic opportunity to work in a fast paced environment on a long 18 months contract. You will be paid and hourly or daily rate.

You will be apart if of my clients growing Health Economics Team, Project Managing Health Economic studies - preparing reports and their design. You will be experienced in Modelling, HTA etc consulting services on behalf of global pharmaceutical clients.

Provides customer-focused leadership in the execution of the start up of sites in one or multiple Phase II through Phase IV clinical trials across all functional Site Start-Up (SSU) areas. Accountable for the delivery of activation-ready study sites on time, on budget, and in compliance with all applicable regulations.

Excellent development role as Junior Project Manager with specialist German Pharma firm

Our Oncology Business Unit is hiring!

An excellent opportunity to join a progressive company where you will get to work on interesting medical device studies. This is suitable for for anyone that has managed clinical sites and investigators that is looking to grow their carer.

Our client, a growing company, are currently looking to recruit a Project Manager.

The role requires an in depth understanding of clinical trials supplies. The right candidate needs to have excellent communication skills, verbal and written, be well organised and to manage their time and the workload of their team.

Regulatory Affairs Manager (VAUD, Switzerland, IVD, devices,RA)

Regulatory Affairs Manager (VAUD, Switzerland, IVD, devices, RA, Project management)

Job title: Regulatory affairs manager

Location: Vaud, Switzerland

Company: Medical device & Pharma Industry

Salary: CHF base (130,000-145,000)

Associate Study Manager/ Junior Project Manager. Are you an experienced Lead or Senior CRA looking for the next step within your career? A highly respected, global organisation are currently seeking a Associate Study Manager to join their expanding team. You will be working within the companies Oncology department and will be given the opportunity to become specialists within Oncology clinical trials.

At INC we understand the need for quick site start-up and our average start up time is four weeks quicker than the industry average. We are recruiting for a Site Start Up and Regulatory Project Manager to manage the submissions process on an international level.

My client design, develop and manufacture a wide range of devices that are used for the treatment of cardiovascular and endovascular disease including market leading products for cardiovascular, peripheral intervention, vascular closure systems and solutions for the treatment of structural heart disease.

Our Oncology Business Unit is hiring!

Our Oncology Business Unit is hiring!

Description: Key People are looking for a Senior Clinical Project Manager of Medical Affairs to work with one of our Global Pharmaceutical Clients based in the Basel region of Switzerland. The successful candidate will have expansive Project Management experience in Medical Affairs Trials. They must also have experience of Writing Protocol and have experience in Line Management. The role is 100% office based in the company's head office in Basel. ...

Detailed Job Description

Responsible for the operational implementation of the clinical study strategy related to biosamples, including pre-selection, pharmacodynamic, predictive, and safety markers and PK samples, in collaboration with line function (LF) representatives. Accountable for the timely operational execution of these assessments in Oncology protocols, in compliance with processes and regulatory requirements.

1. ...

A multi-national company with a presence in many countries around the world need to recruit a Project Manager for their Combination Products Research & Development team based close to Zürich, Switzerland

Exciting opportunity for Project Manager with global clinical research organization.

Our client is a fast growing CTMS and EDC provider who are seeking a Project Manager for their Horsham office.

Project Manager Onkologie – Germany Unser Kunde ist ein international führendes Unternehmen für klinische Forschung, die eine breite Palette von Dienstleistungen für die Pharma-und Biotechnologie-Industrie bieten. Als einer der führenden CRO, Sie bieten großartige Chancen und Karrieremöglichkeiten für ihre Mitarbeiter zusammen mit ein grosszuegiges Gehalt und Sozialleistungen.

We are working on behalf of an exciting consultancy who are seeking a project manager. The role you will play will be to lead the design, conduct and communication of several HEOR studies, working in collaboration with research analysts. As an associate project manager, you will conduct HEOR studies, participate in their design and prepare reports and communications.

***Regulatory Affairs Senior Manager CMC Biologics *** Basel, Switzerland *** Provide Strategic leadership for CMC bio projects *** Excellent pipeline *** Contact Marc Van de Voorde or Theo Moore on +41-(0)41 710 51 00 or +44 (0) 207 801 3384

My innovative and expanding medium sized Pharmaceutical client is seeking a regulatory professional with 7+ years broad experience in regulatory affairs covering both pre and post marketing phases of development for a range of therapeutic categories and dosage forms. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380 - or Marc Van de Voorde in our Swiss office, on +41 41 710 5100

Project Manager (within Medical Affairs) Looking for candidates with strong project management / vendor management experience. Candidates MUST have worked within late Phase (III-IV) with an interest and understanding of working in Phase IV. Ability to interact with commercial / science and marketing functions

A fantastic opportunity for an experienced Senior Project Manager to join a world-class CRO - home-based nationwide

Learn how to provide leadership for regulatory submissions whilst providing strategic and innovative thinking for major pharms and biotech projects/submissions (for EU and/or International territories) - If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380 - or Marc Van de Voorde in our Swiss office, on +41 41 710 5100

You will be apart if of my clients growing Economic Modelling team. This role will give you global exposure to all clients within the Pharmaceutical, Biotechnology & Medical Device industry.

Just Pharma are currently looking for experienced Clinical Team Leaders / Managers, Clinical Project Managers or similar level who want to progress into full project management. These positions are being offered across Europe with some home working available.

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

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

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.

My leading Biopharmaceutical client is looking for an experience and motivated CMC bio senior manager to take the lead on a number of projects. You will be working with an excellent pipeline in a strong team, where the focus is on high level strategic input Contact Theo Moore +44 (0) 207 801 3384 or email on cv@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

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