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EU Clinical Trials Manager

Employer
Thornshaw Recruitment
Location
Dublin (City), Leinster (IE)
Salary
Neg
Start date
3 Oct 2022
Closing date
2 Nov 2022

Job Details

My client, a clinical stage biopharmaceutical company with a Global presence now have an amazing opportunity for a Clinical Trials Manager to join the start up in Dublin.

We are seeking a highly motivated professional for a (Snr) Clinical Trials Manager (CTM) role to be the European lead on one or more clinical trials. The CTM is responsible for planning, execution, and coordination of all activities in Europe required to initiate, manage, and complete clinical trials of moderate to high complexity in collaboration with the Global CTM, Clinical Program Manager (CPM) and/or Associate Director (AD) Clinical Operations, Medical Monitor, and other internal and external cross-functional team members.

 

 

 

Your role will act as a European clinical trial lead on one or two clinical studies and work closely with the Global CTM and CPM, to provide European expertise and guidance to clinical study team(s). 

 

 

 

You will collaborate with CRO to manage site related interactions and serves as a liaison and resource for investigational sites.

 

 

 

You will manages assigned clinical trial with minimal oversight. 

 

 

 

Education and Experience:  

 

 

 

  • University degree and relevant clinical trials experience in pharmaceutical, biotech or CRO setting including clinical trial management experience. An equivalent combination of education and experience may be considered.  People management experience is preferred. Prior experience in lead role of global clinical trials is required. CRO/vendor management and oversight experience are required. Oncology clinical research experience is preferred.

 

 

Skills and Abilities: 

 

  • Proven interpersonal skills with the ability to work collaboratively as a member of a cross-functional team. Excellent communication and organizational skills and the ability to work effectively in a high paced, fast changing environment. Thorough knowledge of FDA/EMA, CFR, and GCP/ICH requirements. Exceptional attention to detail. Proficiency with MS Office products (Word, Excel, PowerPoint, SharePoint) and other electronic systems (e.g., Veeva eTMF) and databases (e.g., Medidata RAVE EDC). Experience with Zoom, Smartsheet and Spotfire is helpful. Previous experience with database build is an asset. Ability to travel for site co-monitoring activities, vendor visits/audits as required (up to 30%). Adhere to the highest degree of professional standards and strict confidentiality on matters that require discretion.  Lead and develop team of clinical professionals. 

 

 

If you would like to learn more about this amazing opportunity, please send your CV to tdunne@thornshaw.com or ldunne@thornshaw.com or call Linda or Tina at +353 1 2784674/2784701

 

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

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

 

Company info
Website

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