Skip to main content

Labcorp hiring fresher for reporting associate.

Labcorp hiring fresher for reporting associate




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
Learns to and reviews written contact with clients.
Prepares form letters and communication text.
Assists other client-facing staff (e.g., study director) with organizing client site visits and client conference calls
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.
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.
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
Learns to and prepares the study report using details described in the protocol, protocol amendments, and study communications and Covance or client-specific requirements
Learns to and incorporates contributions (e.g., protocol, protocol amendments, certificates of analysis, contributor reports) into the draft report
Learns to and prints, binds, and mails draft and final study documents
Learns to and addresses quality assurance inspection items on GLP-regulated studies
Learns to and finalizes study reports and obtain, prepare, and deliver materials to archives
Learns to and prepares report amendments
Learns to and assists in the preparation of tabulated summaries in association with the study director
Data Table Preparation
Learns to and prepares data tables including completing basic statistical analysis in table generation programs.
Learns to and drafts and quality checks data tables that were manually prepared
Learns to and reviews data tables for accuracy
Scheduling Responsibilities
Learns to and reviews and adjusts the reporting schedule to ensure client expectations are met 
Learns to and schedules and coordinates study report finalization efforts

Experience:

0 - 1 years of experience
Professional writing or data tabulation experience, especially in pharmaceutical research or life sciences, will be helpful. 
Basic knowledge of office software (e.g., Microsoft® Office, especially Word and Excel; Adobe® Acrobat®)
Attention to detail, time management skills, and organizational skills

:

Master's in Pharmacy or any other life sciences will be required.

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


Comments

Post a Comment

Popular posts from this blog

TCS Sigma hiring 2024 b.pharm/m. pharm fresher can apply

TCS Sigma hiring 2024 b.pharm/m. pharm fresher can apply.  Tata Consultancy Services tata.com CONTACT US TCS WORLDWIDE TCS CAREERS TCS INDIA CAREERS Envision excellence, blaze new trails! TCS Sigma Hiring registrations are now open for Pharma 2024 graduates and postgraduates group IMPORTANT DATES Registration End Date: 18th October 2023 Test Date: 18th and 19th November 2023 About TCS Sigma Hiring for 2024 year of passing Graduates TCS Sigma is opening its gates for the batch of 2024 Pharmacy graduates & postgraduates to apply for exciting career opportunities. TCS Sigma Hiring: Designed to select the best fresher talent in the country from the class of 2024 to fuel the growth plan of the organization through its business strategy. Exceptional performers will be part of TCS’ fastest-growing units - in various enriching roles that amplify their career growth. Register and make a great start with the upcoming TCS Sigma Hiring before 18th October 2023. Application Pro...
Post a Comment
Read more

ThermoFisher hiring Clinical trial coordinator.

Thermo fisher hiring Clinical Trial Coordinator Location Remote, India  Job Id R-01227106   Job Type Full time   Category Clinical Research   Remote Fully Remote About   Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. Our Clinical Research team, who powers our PPD® clinical research portfolio, are part of our leading global contract research organization (CRO).  Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, ...
Post a Comment
Read more

Medtronic hiring clinical research specialist Mumbai/Gurgaon.

Medtronic hiring clinical research specialist Mumbai/Gurgaon. Job Description Travel Yes, < 50 % of the Time Careers that Change Lives A Day in the Life MAIN PURPOSE OF JOB • Provides all aspects of executional support for Clinical Research Projects/studies in India and Subcontinent countries as assigned • Performs activities for either a specific therapeutic area or across several therapeutic areas. MAIN JOB DUTIES/RESPONSIBILITIES     · Management of global and local clinical studies in Clinical Research Specialist role and execution of clinical projects as required · Provide operational support to clinical studies which includes but not limited to o Ethics Committee (EC) submissions and communications o Contract negotiation and execution support o Site management o Manage site and study team communications o Study document management and filing o Data queries resolution and follow-up with sites · Provide technical support...
Post a Comment
Read more