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Senior Project Manager, Belgium - L

Employer
ClinChoice
Location
Belgium
Salary
Competitive
Start date
14 Sep 2022
Closing date
13 Oct 2022

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Discipline
Project Management
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Description:
Location: Beerse, Belgium - Office

Schedule: Full-time, permanent

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for an international CRO can bring? Our team says it is the best of both worlds....

TalentSource Life Sciences (the sponsor-dedicated division of CROMSOURCE), is searching for a Senior Project Manager to join one of our clients, one of the most innovative pharmaceutical companies in the world.

CROMSOURCE is an international CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with their client counterparts.

The Project Manager should have prior project management experience in a clinical setting, ideally
experience and leadership in projects where real-world data or novel types of patient-level data (data from electronic medical records, genomics, and/or imaging data) have been re-used for clinical research applying privacy-preserving methods

Main Job Tasks and Responsibilities:
  • Defining the overall project strategy for year 3 of the project together with the project
    coordinators and WP leaders and assure the strategic goals are reflected in the project
    management plan and all actions to accomplish this plan (including facilitating steering committee
    and cross-WP meetings).
  • Ensuring timely and accurate documentation and communication of progress and issue
    escalation. Day-to-day monitoring of the project management plan and maki
    adjustments as needed, in close alignment with the work package leaders and the project
    2 coordinators. Leading activities of the ongoing review of progress on deliverables, completion of
    milestones and risk analysis and mitigation.
  • Monitoring project budget and supervising actuals vs forecast expenses and reviewing
    assigned vendor invoices/spend.
  • Managing the identified KPIs to measure outcomes and success for the project,
    ensuring all partners are aligned on the approach to reach these KPIs. Monitoring risk and
    mitigation planning which may lead to deviation of certain KPIs.
  • Providing leadership and project management for the emerging sustainability initiatives
    which must create mid and long-term value for each of the consortium partners. Support
    the consortium in identifying these most appropriate sustainability projects and helping to
    build the Return-on-Investment case and business plan for the sustainability phase.
  • Leading the communication, including supporting internal and external dissemination
    activities to ensure value generation for all consortium partners.
  • Successful project closeout, assuring all administrative and financial requirements are
    fulfilled and making the project and its deliverables audit ready

Education and Experience:
  • An advanced biomedical sciences degree is preferred (Master's/PhD/PharmD degree) with a minimum of 10 or more years of total business experience required.
  • A minimum of 6 years of project management experience in global clinical research either in a
    CRO, Pharma, consultancy or other clinical trial sponsor environment is preferred.
  • Proven experience in managing and executing complex projects from start to finish.
  • Excellent organizational, project management, and influential management skills, complemented
    by a "hands-on" operational and business planning orientation is required. PMI (or equivalent)
    certified.
  • Experience leading public-private partnerships/consortium projects.
  • Familiarity with and interest in health technology and health information technologies is
    required; direct experience with health information technology, healthcare technology, and
    mobile health applications are highly preferred.
  • Experience with real-world evidence and data sciences is preferred.
  • Experience contributing to innovative analytical solutions is preferred.
  • Experience with management and supervision of vendors is preferred.
  • A self-starter with a strong results orientation, who can operate independently and can navigate
    complex, matrixed environments are required.

Specific Role Requirements and Skills:
  • Outstanding communications skills, both written and oral, capable of effectively summarize
    abstract concepts into clear, concise, and insightful business cases.
  • Experience collaborating successfully with global clinical teams, R&D Operations, Therapeutic
    Areas and Medical Affairs are preferred.
  • Strong team player, motivating professional colleagues and stakeholders cross-functionally and
    across organizations within the consortium.
  • Fluent in Dutch and English, must be based in Belgium


Our Benefits of Working for TalentSource in Belgium:
  • Competitive Salary
  • Group and hospitalisation insurance
  • Electronic meal vouchers
  • Internet reimbursement
  • Dedicated Line Manager
  • Regular face-to-face or phone meetings with the line manager
  • Full annual performance review process
  • Ad-hoc team events and end-of-year party
  • Career opportunities within both our CRO departments and our TalentSource Life Sciences Unit, locally and internationally
  • Employee satisfaction survey - your feedback is important for continuous improvement


The Application Process

Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements we need, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

If you would like to discuss the role before applying through the website @ https://www.talentsourcelifesciences.com/jobs please contact careers@cromsource.com for more information.

Who will you be working for?

About CROMSOURCE

CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.

Our Company Ethos

Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE 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 all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.

About TalentSource Life Sciences

TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role, and work autonomously.

CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Keywords: Clinical Project Manager, Senior Clinical Project Manager, Project Leader, Study Manager, PM, PL, SM, Senior Project Manager, Project Manager, Cancer, Oncology, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated.

Skills: Oncology, Clinical Project Manager, Clinical Study Manager, Senior Clinical Lead, Outsourcing, Project Leadership, English, French Location: Belgium Share:

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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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