Asst I PSS

Description

Labcorp Drug Development

As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.

Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.

Did you know?

In July 2022, Labcorp announced its intention to spin off its clinical development business as a separate public company, subject to the satisfaction of certain customary conditions. Fortrea will become the new brand identity for our Clinical Development business in connection with the spin-off, which is expected in mid-2023.

We believe that the exceptional is possible when you have the right partner, so we are looking for the right people to help build a transformative force in Clinical Development. www.fortrea.com

These statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties*.

• Perform case intake and triage of the incoming safety information or reports from various sources either spontaneously or from a clinical trial
• Assist with processing of the adverse events, including but not limited to:

Data entry of safety data onto adverse event tracking systems

Write patient narratives & code adverse events accurately using MedDRA (for Marketed products, if applicable)

• Assist in the listedness assessment against appropriate label (for Marketed products, if applicable)
• Assist in generation of queries and collection of missing or discrepant information in consultation with medical staff, if needed
• Submission of expedited SAE reports to clients, regulatory authorities, ethics committees, investigators, 3rd party vendors, Partners and Labcorp project personnel, as required within the agreed timelines.

• Assist with processing and submission of expedited and periodic reports to worldwide regulatory agencies or other recipients (Clients, Regulatory Authorities, Ethics Committees, investigators and Labcorp project personnel etc), and prioritise the reports for processing and submission within the regulatory and/or study specific applicable timelines.

• Assist in the reconciliation of databases, as applicable
• Work within the Quality Management System framework, including but not limited to Standard Operating Procedure (SOP), departmental Work Instructions (WIs) etc as appropriate
• Assist in the maintenance of supporting files/ documentation regarding adverse event reporting requirements in all countries, if applicable
• Support upload/archival of case/study/project documentation, as appropriate
• Build and maintain good PSS relationships across functional units
• Support compliance of operations with governing regulatory requirements
• Any other duties as assigned by management
• The above job duties are completed by the staff as applicable, depending on the role they are assigned to.

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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