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Clinical Research Manager

Introduction


For one of our clients, XPE Pharma & Science is looking for a Clinical Research Manager.


Function information


Description:

Operating on behalf of the Medical Device Group, this individual will have strong scientific expertise to provide insights and strategic direction to develop innovative evidence generation and dissemination strategies (EGS / EDS) for New Product Development and Life-Cycle Management (NPD and LCM) projects; 

Overall responsabilities:

  • Reports to the Franchise Platform Leader or Sn Clin Res Mgr, MD CR&D; 
  • Responsible for Clinical R&D activities for assigned projects, including: 
  • Develop and deliver appropriate Global EGS / EDS to support NPD and LCM within the assigned platforms, with collaborative relationships with all relevant CR&D partners and cross-functional partners (e.g. Global Strategic Marketing, Medical Affairs, Regulatory Affairs, HEMA, R&D, etc), ensuring cross- functional alignment; 
  • Responsible for delivery of assigned clinical projects, through effective partnership with the Clinical Operations and BSDM teams, to enable optimized engagement leading to delivery of clinical project commitments (delivery on time, within budget and in compliance with regulations and SOP); 
  • Ensure input and strong alignment from key regional MD CR&D leads and other strategically important countries/regions in the development of the EGS / EDS; 
  • Lead in study design to develop appropriate clinical trials to meet the NPD / LCM needs; 
  • Lead in appropriate interpretation and dissemination of all evidence generated, based on EDS, including Clinical Study Reports, abstracts, manuscripts, CERs etc 
  • Contribute in clinical scientific discussions with regulatory agencies / notified bodies to drive support of the clinical and regulatory strategy, including proposed clinical investigations; review process of clinical evidence generated for marketing authorization, line extensions, etc, including during sponsor regulatory inspections; 
  • Responsible for team’s interface and collaboration with key opinion leaders, investigators, IRB’s/EC’s, Regulatory Agencies, societies, associations, etc; 
  • Foster strong relationships with external stakeholders to shape and influence relevant policies, etc 
  • Partner with internal stakeholders to ensure accurate dissemination of clinical data/evidence in value briefs and technical summaries for market access and reimbursement.

Requirements


Functional and Technical Competencies: 

  • Thorough understanding of clinical research science and processes along with a broad and extensive understanding of product development processes, team dynamics, related healthcare market environment, clinical trends, and global clinical trial regulations; 
  • Ability to provide strategic and scientific clinical research input across NPD and LCM projects, including complex and / or transformational projects; 
  • Proven track record in delivering clinical programs within clinical / surgical research setting, on time, within budget and in compliance to SOPs and regulations; 
  • Comprehensive understanding of clinical trial regulations across multiple regions; 
  • Ability to lead teams to deliver critical milestones, including complex projects; 
  • Ability to collaborate across different functional areas within CR&D to ensure alignment with governance processes (assigning roles and responsibilities, setting priorities, managing deliverables, etc). and to meet business objectives; 
  • Demonstrated ability to build collaborative relationships with key internal and external partners and stakeholders; 
  • Leadership requirement – ability to influence, shape and lead without direct reporting authority;
  • Change agent in team development and progression; 
  • Experience in effective management of project budget processes.

Leadership Competencies: 

Strong leadership required in alignment with the intern Leadership Imperatives: Connect, Shape, Lead, Deliver as noted below. 

  • Connect - foster strategic partnerships with key internal & external stakeholders to ensure development and timely delivery of innovative EGS / EDS 
  • Shape – build strong relationships with external stakeholders to shape and influence relevant policies 
  • Lead – continually develop expertise to provide strategic and scientific clinical research capability 
  • Deliver – ensure clinical programs are delivered on time, within budget and in compliance to regulations and SOPs 
  • Know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times. 
  • Diligently participate in our compliance program-related activities as denoted by your supervisor or our Chief Compliance Officer. 
  • Performs other related duties as required. 

Education and experience requirements:

  • A Bachelor’s degree in Biological Science or related discipline 
  • A minimum of 8 years related scientific / technical experience, including leadership / management role within Clinical Research.

Offer


Working as a consultant for XPE Pharma & Science means that you will be a part of the Adecco group. You will be guided and be followed-up by one of our Talent Managers. While giving the best of yourself at your project you will be able to develop your soft & hard skills as well via our Talent Managers.

We offer you a permanent contract full-time in an international lifescience environment and a Great place to work!


Information


Sybille Ponet

sybille.ponet@xpepharmascience.com

02/801.16.65


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