Leading worldwide life sciences corporation Labcorp offers crucial data to support doctors, hospitals, pharmaceutical firms, researchers, and patients in making informed choices. We offer insights and speed up innovations to improve health and quality of life through our unmatched diagnostics and medication development capabilities. As we revolutionise methods of patient care, you can join our team of more than 75,000 workers who serve customers in more than 100 different countries.
Job Role : Reporting Associate I
Education: Master’s in Pharmacy or any other life sciences will be required.
The Reporting Associate I learns and performs the duties of drafting and finalizing nonclinical study reports and completes the following duties with limited supervision.
General Duties
1. Learns to and reviews written contact with clients.
2. Prepares form letters and communication text.
3. Assists other client-facing staff (e.g., study director) with organizing client site visits and client conference calls
4. Learns to and uses software tools to efficiently and accurately complete job duties. Types of software include word processing, spreadsheet, table generation, collaboration/sharing, and database applications.
5. After completion of sufficient training, manages a full study workload with complex study designs by adhering to report preparation schedules and prioritizing tasks. Identifies and resolves changes to established study schedules to ensure client deliverables are met.
6. After completion of sufficient training, begins to learn leadership within the reporting solutions group on activities such as performing peer reviews, preparing and delivering presentations, participating in staff meetings, participating in process improvement projects, and/or liaising with cross-site staff.
Report Preparation
1. Learns to and prepares the study report using details described in the protocol, protocol amendments, and study communications and Covance or client-specific requirements
2. Learns to and incorporates contributions (e.g., protocol, protocol amendments, certificates of analysis, contributor reports) into the draft report
3. Learns to and prints, binds, and mails draft and final study documents
4. Learns to and addresses quality assurance inspection items on GLP-regulated studies
5. Learns to and finalizes study reports and obtain, prepare, and deliver materials to archives
6. Learns to and prepares report amendments
7. Learns to and assists in the preparation of tabulated summaries in association with the study director
Data Table Preparation
1. Learns to and prepares data tables including completing basic statistical analysis in table generation programs.
2. Learns to and drafts and quality checks data tables that were manually prepared
3. Learns to and reviews data tables for accuracy
Scheduling Responsibilities
1. Learns to and reviews and adjusts the reporting schedule to ensure client expectations are met
2. Learns to and schedules and coordinates study report finalization efforts
Experience:
1. 0 – 1 years of experience
2. Professional writing or data tabulation experience, especially in pharmaceutical research or life sciences, will be helpful.
3. Basic knowledge of office software (e.g., Microsoft® Office, especially Word and Excel; Adobe® Acrobat®)
4. Attention to detail, time management skills, and organizational skills
Job Location: Bangalore
 
 
 
