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Clinical Laboratory Data Manager

labcorp

Full-time
Poland
project management
documentation
communication
biotech
automation
Apply for this position

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 is remotely based.

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 in a scientific field or equivalent education

  • Clinical Data Management and/or Clinical Trials experience.

  • Client facing 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:

Labcorp strives for inclusion and belonging 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 and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), 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. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

Apply for this position
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About the job

Full-time
Poland
9 Applicants
Posted 2 days ago
project management
documentation
communication
biotech
automation

Apply for this position

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Clinical Laboratory Data Manager

labcorp

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 is remotely based.

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 in a scientific field or equivalent education

  • Clinical Data Management and/or Clinical Trials experience.

  • Client facing 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:

Labcorp strives for inclusion and belonging 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 and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), 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. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

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