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Job Details

Senior Clinical Project Manager

Company: CROMSOURCE
Location: Belgium
Reference: HQ00001168
Closing Date: 25 Mar 18
Type: Permanent
Salary (£): On Application
Benefits: Excellent and Comprehensive Benefits – see below

Job Summary:

Senior Clinical Project Manager (Freelancer also considered) Location: Zaventem, Belgium Start-date: As soon as possible   TalentSource Life Sciences, a division of CROMSOURCE, is currently seeking an experienced Clinical Project Manager (CPM), to join an unique company, focused on helping patients via blood transfusion in different domains like, oncology, pediatrics, medical devices,… This is THE opportunity to join an innovating, unique company, where they believe...

Requirements:

Senior Clinical Project Manager (Freelancer also considered)

Location: Zaventem, Belgium

Start-date: As soon as possible

TalentSource Life Sciences, a division of CROMSOURCE, is currently seeking an experienced Clinical Project Manager (CPM), to join an unique company, focused on helping patients via blood transfusion in different domains like, oncology, pediatrics, medical devices,… This is THE opportunity to join an innovating, unique company, where they believe in the potential of blood to do even more for patients than it does today.

Scope of the function:

The Clinical Project Manager has to manage the overall operational implementation of post-market clinical trials in the EMEA region. For this particular position our client is looking for a CPM who will manage blood transfusion trials in oncology, pediatrics and hematology-oncology. For another project the CPM will be responsible for a medical device study. These are international studies with sites across Europe (Belgium, Spain, Russia and Portugal)

Responsibilities:

  • Operational aspects of clinical trials: review and potentially write study protocol, investigator recruitment, patient enrollment, trip report review, study trackers,…
  • Set up and manage Contracts together with legal department
  • Assist in development study budget
  • Prepare file for ethics submission
  • Monitor progress of project and protocol alignment
  • Write final report with conclusion of primary end-point
  • Participate in study site visits Work with 3 local site monitors (1 for Russia, 1 for Spain/Portugal, 1 for Belgium/France)

Requirements:

  • Master degree or PhD in Biological Sciences, or science related
  • Minimum 6 years of experience and/or training in managing clinical trials, one of which includes leading global clinical trials or global project management
  • Experience conducting all phases of multi-center clinical trials either in medical device, diagnostic, or pharmaceutical industry
  • Knowledge of clinical study (GCP) and good working knowledge of regulatory requirements (ISO, FDA, ICH), both US and International

Skills:

  • Demonstrates effective leadership, management, cross-functional team skills, self-direction, and ability to work independently
  • Demonstrates ability to function independently and cooperatively, and exercises judgment in developing methods, techniques and evaluation criteria for obtaining solutions and resolving problems.
  • Must have a positive and proactive approach to identification and definition of problems, leading to proactive development and implementation of solutions
  • Requires a high level of adaptability, initiative, and willingness to take ownership and accept responsibility for actions and decisions of the team
  • Good organisation skills
  • Demonstrated ability to communicate effectively both verbally and in writing
  • Demonstrated ability to interact with diplomacy and tact while maintaining appropriate assertiveness and persistence
  • Knowledge and use of relevant PC software applications, Microsoft Office

Benefits working for TalentSource:

  • Competitive salary package with extra-legal advantages, company car with international fuel card
  • To become part of a Clinical Research Organisation (CRO), where you have the opportunity to learn and to get different experiences with different clients, in different domains, but maintain job security with CROMSOURCE.
  • Dedicated line manager
  • Follow-up meetings

If you have the experience needed for this position, please contact Vanessa Verdickt, Consultant TalentSource Life Sciences Unit, and send your CV in Word format to vanessa.verdickt@cromsource.com.

Why TalentSource Life Sciences/CROMSOURCE:

CROMSOURCE is a family-owned, high quality ISO-certified international provider of outsourced services to the pharmaceutical, biotechnology and medical device industries. Since 1994, we have been supporting our clients with outstanding clinical research and staffing solutions services. TalentSource Life Sciences is a fully dedicated flexible resourcing unit within CROMSOURCE and the successful growth has been achieved by putting high quality and client focus at the heart of everything we do.

Our employees are the most valuable company asset and we value resources and ensure they work in a friendly, family environment and develop their skills and talents. Human Resources is the fulcrum around which all activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel clear tools to manage both internal and client processes with the same methodology.

Our approach is to equally value our clients and our own people. We know that we are not simply providing 'staff' or 'resources'. We are providing expert people. Highly talented, well trained, motivated people who make a positive difference to the work of our clients every day. Together we help our clients succeed in their work developing medicines and medical devices for patients around the world. Our large management team consists of a people with an extended experience within pharma and a high level of market knowledge. We our open, friendly and approachable and aim to support you through the recruitment process every step of the way.

As this position is client-facing, the successful candidates must be confident and be able to drive the role and themselves and to work autonomously in close liaison with a line manager at TalentSource, who will provide you with mentoring and guidance.

To ensure the success of our clients, our team of international professionals is focused on continuous improvement. We invest in our employees by providing the coaching and training necessary to deliver high quality services for our clients.

Every day we strive to create an environment in which all employees can contribute to their full potential and at the same time allow the company to develop and grow with them. With CROMSOURCE you will be able to participate in exciting projects and achieve your professional goals.

Skills: Senior Project Management, blood transfusion, budget management, oncology, pediatrics, onco-hematology, international

Oncology, Clinical Project Manager, Senior Project Manager

Apply for this job: Senior Clinical Project Manager

Contact Information:

Address:  UK Office
CROMSOURCE Suite 3 Lomond Court Castle Business Park Stirling United Kingdom
FK9 4TU
Scotland
Tel:  +44 (0) 1786 468990
Website:  Visit Our Web Site

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