Study Coordinator Data Management

vor 2 Wochen

Genf, Genf, Schweiz Labcorp Vollzeit
Get ready to redefine what's possible and discover your
extraordinary
potential.

Here at Labcorp, you'll have the opportunity to personally advance healthcare and make a difference in peoples' lives with your bold ideas and unique point of view.

With the support of
exceptional
people from across the globe and an
energized purpose, you'll be empowered to own your career journey with mentoring, training and personalized development planning.


Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow's drug development challenges, creating new possibilities for our clients—and your career.


The Company - LabCorp:


As one of the world's largest and most comprehensive drug development services companies, LabCorp has helped pharmaceutical and biotech companies develop one-third of the all prescription drugs in the marketplace today.


The Position:


At Labcorp we are looking to
expand our Global Data Management team and we are hiring a
Study Coordinator Data Management.


In this role, you act as the secondary liaison between Labcorp and Sponsors, to ensure the successful management of global projects through compliance with the Labcorp strategy, in order to deliver outstanding customer satisfaction.

The position can be located remotely in the UK, Switzerland, Germany or in Belgium.

Responsibilities/Duties:

  • Work in collaboration with Clinical Data Management colleagues to assist in daytoday activities as assigned.
  • Support Clinical Data Manager during start up by:
  • Creating protocol folders for study documentation
  • Adding entries into individual protocol spreadsheet
  • Act as a data liaison between Clinical Data Management and all other Labcorp departments and business units.
  • Complete Quality Assurance tasks as assigned, while adhering to both internal processes and regulatory standards.
  • Quality Check (QC) test files.
  • Deliver test files to clients and log into the metrics tool.
  • Obtain client approval and store auditable documentation.
  • Provide ongoing client support (study maintenance)
  • Address errors and client issues including queries.
  • Participate in studyrelated meetings.
  • Collaborate with clients regarding study modifications.
  • Maintain auditable documents.
  • Facilitate Data Management functions of endtoend data lock processes.
  • Review the data transfer calendar and ensure that it is accurate.
  • Review the properties of data files and error reports. Inform Data Managers of any findings and followup as needed.
  • Ensure that all assigned transfers are completed each day.
  • Attend training to increase Associate Data Manager's capabilities (including corporate, departmental and sponsorrelated training)
  • Ensure uninterrupted client service.
  • Support peers by sharing technical knowledge and customer service skills.
  • Back up peers as needed.

Qualifications:

  • Customer Service experience.
-
Proven Data Management and/or Clinical Trials experience.

  • Any Pharma and/or health industry experience preferred
  • Ability to use standard Microsoft suite of software products.
  • Conversant with databases and database terminology.
  • Strong technical aptitude.
  • Strong organizational, planning and criticalthinking skills.
  • Wellpolished, inclusive, and engaging communication skills (written and verbal) in English.
  • Strong negotiation skills to facilitate, guide, influence, and produce a unified approach within a global, crossfunctional environment.
  • Ability to handle multiple tasks in a timely and professional manner under demanding conditions.

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.

We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.

We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement.

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