Clinical Data Manager, Europe – Home Based (Remote)
Are you a Clinical Data Manager interested in a new challenge with an award-winning, global CRO?
Clintec is a business built around people who strive for excellence, and we currently have an exciting opportunity available for an experienced Clinical Data Manager to join our team in Europe supporting various clients. The role will be home based, so we can consider candidates working remotely anywhere in Europe.
As a Clinical Data Manager you will be responsible for the day-to-day operational data cleaning activities and general administrative tasks involved in clinical trials including trial start-up, conduct, and close-out activities. You will work independently as well as in conjunction with other members of the project team and support the Data Leads with project work.
Third party vendor and SAE reconciliation
Supporting with the creation of study start up documents like Case Report Form design, Data Management Plan, Data Validation Plan, eCRF completion guidelines etc.
Completing data entry tasks into the CDMS
Assist with medical coding and database lock preparation
Attending study meetings and meetings with relevant stakeholders
Conduct User Acceptance Testing activities e.g. Create test plan, test scripts, Data Base testing etc.
Upload/File documents into the Trial Master File
Update the study tracker, metric reports and any other relevant trackers
Carry out all general study filing activities with appropriate quality
Mentoring Data Associates / junior team members for DM activities
WHAT WE NEED:
To be successful in the role of Clinical Data Manager we require candidates with:
Previous significant experience in Clinical Data Management within a CRO or pharmaceutical company
Ideally, Degree level Education
Knowledge and experience of the full clinical trial cycle
Strong communication skills with the ability to interact with internal and external stakeholder at various levels
Experience of mentoring and training junior staff
Previous experience working in Oncology and Cardiovascular clinical trials
WHY JOIN CLINTEC?
At Clintec, we understand that our people are our biggest asset and we value the hard work and dedication of all our employees.
By joining the Clintec team you can expect:
A competitive salary and benefits packages which includes 25 days annual leave, flexible working hours, private health care, life assurance and an attractive pension contribution scheme
Real career development opportunities and a life-long career with an innovative, forward-thinking clinical research company
Click Apply Now to send your CV of email us directly on firstname.lastname@example.org for more information!
Clintec (an IQVIA company), established for 22 years, is an award-winning, full-service global clinical research organisation with our HQ office based in Scotland, UK. We support key product development and manage clinical trials in over 50 countries worldwide, across all major therapeutic areas, with expertise in Oncology and Rare Disease studies. We differ from other players in the clinical research industry as we combine the agility and flexibility typical of smaller CROs with the global coverage and management associated with large CROs.
Find out more by visiting www.clintec.com
Clinical Data Manager / Data Manager / RAVE / Medidata Rave / Data Management / Data Programming / CDMS / Clinical Data Management System / EDC