Clinical Trial Associate

Docs Global (Continental Europe)
Closing date
18 Sep 2020

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Clinical Research, Clinical Trials Manager / Administrator
Full Time
Contract Type
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The role of the CTA is to assist Managers in fulfilling its site management activities and obligations in relation to clinical studies as the primary sponsor of those studies.

Roles and responsibilities:
* Provides support to all study related activities: study start-up activities, including creating site folders, collating, preparing and maintaining documents, updating systems, supporting close out activities
•* Ensures collection, review, track and provision of appropriate clinical documents to support regulatory submission and to perform IRB/IEC submissions including when appropriate preparation and submission of all documents to the central and/or local committee
•* Organise and participate in Investigator meetings and monitor workshops as required within budget guidelines
•* Provide administrative support such as word processing, photocopying, faxing, filing, managing correspondence, presentations preparation, basic computer software support
•* Interacts with Clinical Research Services Manager for project or study related work
•* Supports the execution of clinical studies
•* Manages logistics and document exchange between clinical sites and company
•* Actively contributes to results oriented department goals
•* Identifies opportunities and best practices with local and regional partners that will contribute to overall operational effectiveness

Preferred qualifications:
•* BA/BS/BSc in the life sciences or RN
•* Work experience in life sciences or medically related field, including biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
•* Clinical trial process experience
•* Work involving data entry into systems/databases and/or business support role

Attention to detail *** Time management ***Flexibility ***Relationship management *** Organizational skills *** Written and oral communication skills *** Language skills: English ***Team Work

DOCS provides global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry. 


Our Values

At DOCS, we are driven by our core values that guide our culture and support our goal to become a Trusted Partner. Our five core values are:

OUR PEOPLE: We attract, source, develop and retain the best talent to enables us provide world-class people and solutions for our clients.

EXCELLENCE: We never stop looking for new, better ways of working.

ACCOUNTABILITY: We take responsibility for our actions, owning our client’s problems and proactively looking for solutions.

INTEGRITY: Becoming a trusted partner means being honest, respectful and ethically sound, at all times.

OPENNESS: We encourage and facilitate an open and inclusive environment for a diverse global network of employees and stakeholders.

Contact Us
  • 2 Globeside
  • Globeside Business Park
  • SL7 1HZ
  • United Kingdom
  • +44 (0) 2380 688500
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