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Clinical Trial Leader, Belgium - L

Employer
ClinChoice
Location
Belgium, Brussels area
Salary
Competitive
Start date
11 Sep 2019
Closing date
30 Sep 2019

Job Details

Description:
Job Title: Clinical Trial Leader
Location: Belgium, Brussels area
Contract: Fulltime, permanent, ASAP

TalentSource Life Sciences, the division of CROMSOURCE dedicated to flexible staffing solutions, is currently recruiting for a Clinical Trial Leader to strengthen the team of one of Top 10 Pharmaceutical Companies.

For our client-facing positions, you must be confident and be able to drive the role and yourself and to work autonomously. You will have a close relationship with our Line Managers, who will provide you with mentoring and guidance. Most of our roles are permanent positions with CROMSOURCE and you will be working on studies for just one client. We are open, friendly and approachable and aim to support you through the recruitment process every step of the way.

Job Description:
This individual will be responsible for activities related to site activation (Coordinate EC submission, coordinate CTA execution, Site initiations) for one or several clinical trials within the Clinical Department, as well as fostering strong, productive relationships with colleagues across the organization.

Key Job Activities:
  • Serve as a Clinical Trials Leader within the group to execute company sponsored clinical trials for the Medical Device Franchises under supervision
  • May serve as the primary contact for clinical trial sites
    Manage operational activities of assigned clinical studies within the Clinical group
  • Solves problems with support from Clinical Management arising during clinical trial execution, and will seek guidance for more complex problems, as needed
  • Provide internal communication of important clinical data and events. Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders
  • May be involved in other tasks to support Clinical as needed
  • Track assigned projects budgets to ensure adherence to business plans
  • Support the implementation of new clinical systems/processes, and provide support for publications, as needed
  • Interface and collaborate with site personnel, IRBs/ECs, Competent Authorities/MoH, contractors/vendors, and company personnel
  • Ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliance
  • Provide leadership within a clinical trial, ensuring that each team member has a well-defined set of activities and objectives specific to their role and responsibilities within the context of their business focus
  • Ensure efficient use of resources within the clinical study/program to provide high quality deliverables.
  • Accountable for quality, compliance with regulations and company procedures, timelines, and budgets for assigned clinical trials
  • May assist with the management of large regulated or complex trials under supervision of CTM
  • Identify and ensure strategies, resources, and accountabilities are in place to achieve rapid, high quality execution of assigned clinical trials under his/her responsibilities


Job Qualifications:
  • Minimum of a Bachelor's/University Degree or equivalent required; preferably in Life Science, Physical Science, Nursing, or Biological Science
  • 2-4 years of relevant experience (or equivalent) required
  • Previous experience in clinical trial management or equivalent is required
  • Relevant industry certifications preferred (i.e., CCRA, RAC, CDE)
  • Medical device experience a plus
  • Requires understanding of Good Clinical Practices
  • Good oral and written skills in English
  • Good technical writing skills


If you have the experience needed for this position, please apply directly to https://www.talentsourcelifesciences.com/job-information/?job-id=HQ00001961 . If you would like to discuss the role before applying through the website, please contact Julie.casteleijn@cromsource.com for more information.

Our benefits when working via TalentSource Life Sciences in Belgium:
  • Dedicated Line Manager
  • Employee satisfaction survey - your feedback is important for continuous improvement
  • Annual appraisals development planning
  • Yearly team event
  • New Year's diner
  • Group- and Hospitalisation insurance
  • Electronic meal vouchers
  • Internet reimbursement
  • Company mobile phone (Depending on project)
  • Car with fuel card (Depending on project)


Why choose TalentSource Life Sciences/CROMSOURCE?

TalentSource Life Sciences is a fully dedicated flexible resourcing department at CROMSOURCE, a family owned international, full-service Contract Research Organisation. CROMSOURCE comes from the merger of MSOURCE and CROM and we have been supporting clients with outstanding clinical research and resourcing services since 1994. Successful growth has been achieved by putting high quality and client focus at the heart of everything we do and we are proud to partner with industry leading Pharmaceutical, Biotechnology, Medical Device and Marketing Communications worldwide.

Our employees are the most valuable company asset and because we want to retain our staff, we 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. The success of these core values are evidenced by our current below industry average turnover rates.

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 experts providing experts - 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.

Skills: Clinical Trial Lead, Clinical Trial Manager, ICH-GCP Location: Belgium, Brussels area

Company

ClinChoice

ClinChoice is a recognized and highly respected mid-size, global, full-service contract research organization (CRO) specializing in clinical development, post-marketing, and functional service support. We provide comprehensive end-to-end solutions, taking products from early clinical development to post-approval lifecycle management. We are committed to fostering innovation in the pharmaceutical, biotechnology, medical device & diagnostics, consumer health, cosmetics, and nutraceuticals industries. Since our establishment in 1995, we have consistently delivered high-quality services and solutions throughout the entire development lifecycle of our clients’ products. We serve a wide-ranging clientele that encompasses six of the top ten pharmaceutical companies, leading medical device companies, preeminent biotechnology companies, the largest consumer health and cosmetics companies, and numerous small-to-mid-sized innovator companies. With over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific, we are positioned to fulfil our clients’ needs locally and globally.

 

We’re on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.

 

Company info
Website
Telephone
+44 1628 566121
Location
Suite G48
268 Bath Road
Slough
Berkshire
SL1 4DX
United Kingdom

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