Coordinator Support I at Labcorp
Bengaluru, karnataka, India -
Full Time


Start Date

Immediate

Expiry Date

30 Aug, 26

Salary

0.0

Posted On

01 Jun, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Publishing, Document Modification, Quality Control, Project Documentation, Language Translation Coordination, Time Management, Attention To Detail, Communication, Organization, Computer Literacy

Industry

Medical Practices

Description
Labcorp is a global leader in diagnostic testing and drug development solutions, helping healthcare providers, researchers, and patients make informed decisions that advance care. Join us in our mission to improve health and improve lives. Labcorp is seeking a to Clinical Publishing Coordinator to join our team at Brigade Twin Towers, Yeshwanthpur, Bangalore – 560022 Work Schedule Rotational shift Job Responsibilities Follow applicable departmental Standard Operating Procedures, Work Instructions and departmental guidelines. ¨ Complete required trainings according to required timelines. ¨ Complete day-to-day tasks ensuring quality and productivity. ¨ Create and modify clinical investigator manuals, requisitions and other relevant materials according to SOW requirements to provide on-time, quality project related documentation. ¨ Ensure that language translations of assigned project related documents are completed in a timely manner. ¨ Work effectively with peers to ensure delivery of appropriate DP documentation. ¨ Ensure timely escalation as needed. ¨ Other duties as assigned by management Minimum Qualifications Bachelor’s Degree in Science Preferred Qualifications 6 months experience in clinical research and industry. Master's Degree in Science Additional Job Standards ·Perform in a general office setting. · Sit for sustained periods of time in front of monitor. · Perform with multiple interruptions. · Requires the ability to manage multiple priorities. · May be required to work overtime. · Demonstrated ability to organize and communicate effectively. · Demonstrated ability to pay attention to detail. · Ability to work well with others. ·Ability to deliver consistent high quality of work. ·Ability to use computer and departmental tools. 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. We believe in the power of science to change lives. Labcorp is a leading global life sciences company that provides vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations to improve health and improve lives. Here, you can join our nearly 70,000 employees, serving clients in more than 100 countries, as we work together to transform approaches to patient care.
Responsibilities
The role involves creating and modifying clinical investigator manuals and requisitions according to SOW requirements. The coordinator ensures the timely delivery of quality project documentation and manages language translations.
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