Company: SynteractHCR Deutschland GmbH
Location: Brussels, Belgium
Closing Date: 25 May 17
Type: Full Time
Salary (£): On Application
Clinical Trial Master File Specialist (m/f) Overview The Trial Master File (TMF) Specialist supports the clinical study team in all aspects of the maintenance of the study TMF by supporting the Study Delivery Lead (SDL) and document owners and addresses ad-hoc issues being the Trial Master File (TMF) study owner. Responsibilities Ensure high quality and up-to-date TMF management being embedded in different clinical study teams Own and maintain the study TMF...
Clinical Trial Master File Specialist (m/f)
The Trial Master File (TMF) Specialist supports the clinical study team in all aspects of the maintenance of the study TMF by supporting the Study Delivery Lead (SDL) and document owners and addresses ad-hoc issues being the Trial Master File (TMF) study owner.
Academic & Professional Qualifications:
Skills & Experience
What We Have to Offer
Our team-oriented organization is collaborative and diverse; our work is interesting and challenging; and every individual has an opportunity to thrive, grow, and achieve success in his or her position. We are proud of our reputation in the industry for quality services and specialized teams dedicated to meeting or exceeding client expectations
Who We Are
SynteractHCR is a full-service contract research organization with a successful two-decade track record supporting biotechnology, medical device and pharmaceutical companies in all phases of clinical development. With our “Shared Work – Shared Vision” philosophy we provide customized Phase I through IV services collaboratively and cost effectively ensuring on-time delivery of quality data so clients get to decision points faster. Operating in 15 countries, we deliver trials internationally, offering expertise across multiple therapeutic areas including notable depth in oncology, CNS, infectious disease, endocrinology, cardiovascular and respiratory, among other indications.
Our mission is to support the innovation and development of better therapies in healthcare. Our focus on patients’ safety and comfort helps us to establish ethical standards for everything we do.
We are an Equal Opportunity Employer. No job applicant or employee shall receive less favorable treatment or be disadvantaged because of their gender, marital or family status, color, race, ethnic origin, religion, disability or age; nor be subject to less favorable treatment or be disadvantaged on any other basis prohibited by applicable law. Applicants for positions with SynteractHCR must be legally authorized to work in the country which they are applying and verification of employment eligibility will be required as a condition of hire.
Have we sparked your interest? Then we are looking forward to receiving your application! Please apply through our homepage synteracthcr.com and state your earliest start date/notice period and your desired salary. If you have any questions regarding the position please contact antonia.schultze@Synteracthcr.com
SynteractHCR Deutschland GmbH
|Tel:||+49 89 12 66 80 0|
|Fax:||+49 89 12 66 80 2444|
|Website:||Visit Our Web Site|
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