Are you interested in making a real scientific impact through your everyday work? Would you enjoy working in a team-focused environment as you explore unique career opportunities?
If you are looking for a company where you can personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view, consider working at Labcorp Drug Development as a Data Management Study Coordinator.
In this role, you will support our Central Labs Global Data Management team. This position will be remotely based in the United States.
In more details, you will…
Work in collaboration with Clinical Data Management personnel to assist in day-to-day activities as assigned.
Support Clinical Data Manager during start up.
Create protocol folder(s) for study documentation.
Add entries into individual protocol spreadsheet.
Act as a data liaison between Clinical Data Management and all other Labcorp Drug Development departments and business units.
Consult with Medical Affairs via a Med/Tech Affairs Request Form.
Collaborate with Project Management proactively and reactively regarding study questions.
Manage and resolve issues with Specimen Management.
Initiate data changes with the appropriate department and revise all non-compliant requests.
Partner with other Labcorp Drug Development departments and business units, and provide integrated support and process improvements as needed.
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 study-related meetings.
Collaborate with clients regarding study modifications.
Maintain auditable documents.
Facilitate Data Management functions of end-to-end 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 follow-up as needed.
Ensure that all assigned transfers are completed each day.
Attend training to increase Data Management Study Coordinator’s capabilities (including corporate, departmental and sponsor-related training).
Ensure uninterrupted client service
Support peers by sharing technical knowledge and customer service skills.
Back up peers as needed.
Thrive personally and professionally at Labcorp Drug Development
Working at Labcorp Drug Development, you’ll continue to grow in our learning-based culture so you’ll know how to expertly respond and adapt as the industry continues to evolve. Here, you’ll put your education to work as you play a meaningful role in advancing healthcare and making a difference in people’s life.
In addition, Labcorp Drug Development offers great benefits, global experience and the opportunity to work independently within a team-oriented environment.
What we’re looking for
Data Management Study Coordinators are the most successful at Labcorp with:
Education/Qualifications:
High school diploma with minimum two years LabCorp Drug Development experience, or Associate’s degree or equivalent education.Work Experience:
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.
Ability to use standard Microsoft suite of software products.
Conversant with databases and database terminology.
Strong technical aptitude.
Customer Service experience.
Data Management and/or Clinical Trials experience.
Get to know Labcorp Drug Development
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations.
Here, you can join our more than 75,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives.
Salary:$45,000-$60,000
Benefits: All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable. For more detailed information, please click here (https://cdn.phenompeople.com/CareerConnectResources/COVAGLOBAL/documents/Labcorp-Benefits-TheWayWeLive-1659629596356.pdf) .
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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