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Clinical Development Lead

Employer
Thornshaw Recruitment
Location
Dublin (City), Leinster (IE)
Salary
Negotiable
Start date
5 May 2021
Closing date
4 Jun 2021

Job Details

Working with my client on a new vacancy for a Clinical Development Lead.   This is a new role and a fantastic opportunity for someone looking to make their next career move into a dynamic fast paced environment.

Your Role:

To lead the execution of the Company’s clinical development and to manage, plan and

execute the Company’s clinical programme.

Key Responsibilities:

  • Facilitating and developing the design, planning and execution of the Company’s clinical programme which includes ongoing and new observational studies as well as all interventional studies to required international standards
  • Support clinical site selection process overseeing the assessment of sites i.e. sites are adequately staffed and trained to perform the required tasks (protocol adherence, data reporting requirements, IRB reporting, regulatory requirements).
  • Maintaining professional and credible image with key physicians, clinical investigators and consultants, liaising with all these relevant stakeholders to ensure efficient and timely clinical study execution
  • Conducting briefing and technical meetings for internal and external representatives
  • Forecasts and manage study related finances within agreed budgets and communicate on project status to wider team
  • Manage the Contract Research Organisation and independent contractors relevant to the execution of the clinical programme
  • Manage and track study related activities in-house and at site to allow identification and mitigation of any study related issues in a timely and efficient manner
  • Support the running of internal and external meetings as needed by the project.
  • Other duties to include support the development of the technical documents, organising key publications and performing literature searches
  • Identify potential areas for internal process improvement, propose and implement changes following consultation and agreement with all relevant stakeholders
  • Engage with the Company QMS to ensure delivery of the overall quality strategy & support the achievement of the business quality objectives

Willingness to travel to complete work-related activities 

Requirements:

Essential

  • Medical or scientific education with qualification to master's degree level or higher. 
  • 6+ years' experience from similar positions in the clinical trials industry.
  •  

Desirable

Project management qualification

  • Good working knowledge of FDA and ICH/GCP and European Medical Device regulations and willingness to continuously expand medical, scientific, market, and industry knowledge
  • Motivated, self-starter and an organized individual with strong scientific background with the ability to work in teams.
  • Good interpersonal skills and the ability to build strong relationships with key stakeholders.
  • Technically proficient with PowerPoint, excel, word and reference management tools.  

Excellent written and verbal communication skills

For further details contact Tina at +353 1 2784701 or 087 6811990 or email to tdunne@thornshaw.com.   Thornshaw Scientific is a division of the CPL Group. www.thornshaw.com

Company

thornshaw-title

Thornshaw Scientific Recruitment was first established in 1999 and since then has become a leader in Scientific recruitment.  In 2005 we partnered with Cpl Resources, one of Europe’s most successful recruitment companies.

Our wealth of experience in specialised recruitment allows us to offer the right solution to each employer, whatever their recruitment requirements.

Over the years we have developed strong relationships with our clients in the market and we pride ourselves on our repeat business from clients.

Our Industries

We are a global provider and have been providing a reputable recruitment service to the Biotech, Pharmaceutical, Clinical Research, Medical Device, Engineering and Healthcare industries for over 20 years. 

Our Specialities

Clinical Research, Regulatory Affairs, Quality Assurance, Medical Affairs, Pharmacovigilance, Biostatistics, QC, Validation.

Our Mission

thornshaw-ourmission

For further details on our services contact Tina at +353 1 2784701 or email tdunne@thornshaw.com

 

Company info
Website

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