Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.

Labcorp is seeking a Data and Report Specialist I to join our team at Yeswanthpura in Bangalore, Karnataka.

Work Schedule
Monday - Friday -2pm -11pm - 2nd Shift

Job Responsibilities

• The Data and Report Specialist is responsible for supporting activities related to standards, GLP and regulatory guidelines in a timely, efficient manner.
• General assistance to the global Study Delivery team will be an essential part of the role.  Additional daily duties may include support of other functions within
Bioanalytical.
• Primary responsibility is to complete duties associated with supporting the
• Bioanalytical Business and delivery of studies mainly responsible for creating the initial draft of Bioanalytical study reports using study data and work instructions.

• Duties may include, but are not limited to the following:
o Managing tasks in project tracking systems.
o Preparing study reports other materials associated with Bioanalytical studies.
 

• People Responsibilities:
• The position has no people responsibilities as it an Individual Contributor Role

• Essential Job Duties:
• Create the initial draft of Bioanalytical study reports using study data and work instructions.
• Creates sample analysis and validation study plans using source data such as clinical protocols, analytical methods and Bioanalytical SOPs.
• Creates and/or edits study setup information.
• Independent utilization of project tracking systems to track and document data and report completion activities.
• Effectively manages own time and deadlines.
• Effectively manages task status tracking and time recording.
• Perform other duties as assigned.

Minimum Qualifications
• Bachelor's degree in science

Preferred Qualifications
• 6 months experience in contract research industry.
• Master's degree in science.

Additional Job Standards

• Knowledge of GLP/GCP and regulatory requirements is advantageous
• An understanding of GLP/GCP processes and procedures is desirable.
• Basic understanding of contract research environment
• Understanding of regulatory principles.
• Demonstrated ability to organize and communicate effectively.
• Demonstrated ability to pay attention to detail.
• Ability to work well with others.
• Demonstrated computer literacy

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

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