Clinical Laboratory Data Manager

Get ready to redefine what’s possible and discover your **extraordinary** **potential**. Here at Labcorp Drug Development, 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 Drug Development**:
As one of the world's largest and most comprehensive drug development services companies, LabCorp Drug Development has helped pharmaceutical and biotech companies develop one-third of the all prescription drugs in the marketplace today.

**The Position**:
This role falls under **our Global Data Management team **where you will be working as an** Clinical Laboratory Data Manager.**

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

**Responsibilities/Duties**:

- Engage client data management during start up activities which includes:

- Contact clients for initial study discussion and determine authors of Data Transfer Specifications (DTS). Provide recommendations and alternatives to optimize data quality
- Review Statement of Work (SOW) for study scope.
- Ensure start-up packet delivery to clients.
- Collaborate with clients to finalize Data Transfer Specifications and obtain final client approval on Data Transfer Specifications (DTS
- Create standard data transfer format(s) in compliance with client requests while adhering to both internal processes and regulatory standards
- Build and modify Data Transfer formats, including creation of test data as needed.
- Perform Quality Check (QC) test files, and deliver test files to clients
- Obtain client approval and store auditable documentation.
- Provide ongoing client support (study maintenance) which includes:

- Participate in study-related meetings.
- Collaborate with clients regarding study modifications, and new service requests.
- Confirm changes and send files as needed.
- Address errors and client issues including queries.
- Collaborate with Project Management proactively and reactively regarding study questions
- Facilitate Data Management functions of end-to-end data lock processes.
- Maintain auditable documents.
- Partner with other Covance departments and business units, and provide integrated support and process improvements as needed.
- Represent Global Data Management in client visits, audits, inspections and bid defenses as needed.

**Qualifications**:

- BS/BA four-year degree or equivalent education, or 4 years Labcorp experience
- Customer Service experience.
- ** Data Management and/or Clinical Trials experience**.
- 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 critical-thinking skills.
- Well-polished, inclusive, and engaging communication skills (written and verbal).
- Strong negotiation skills to facilitate, guide, influence, and produce a unified approach within a global, cross-functional 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.

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