Covance Recruitment 2021| Freshers

 Covance Recruitment 2021

ABOUT COMPANY:

Covance by LabCorp is the drug development business of LabCorp, where 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 more than 75,000 employees, serving clients in more than 100 countries, as we work together to transform approaches to patient care. Reference.

Overview:

Company Name:	Covance
Company Website:	www.Covance.in
Job Role:	Analyst
Job Location:	Pune, Mumbai
Experience:	Fresher
Telegram Group:	https://t.me/jobstreaks

Job Overview:

• Assist in the processing of expedited safety reports (ESRs).  This includes, but is not limited to: maintenance of adverse event tracking systems set-up and maintenance of project files, core process files and central safety files reporting of ESRs to clients, regulatory authorities, ethics committees,  investigators and Covance project personnel, if required, within study specified timelines.
•  Provide administrative support to PV&DSS personnel (e.g. proof-reading and editing correspondence/documents, mailings, filing, faxing, photocopying and archiving etc).
•  Ensure all incoming faxed Serious Adverse Event (SAE) reports are appropriately stamped, logged into the departmental tracking application and forwarded in a timely manner to the designated Drug Safety Associate (DSA)/Senior Drug Safety Associate (Sr. DSA).
• Ensure submission of client-related documents is sent to the client within designated timeframes (e.g. SAE reports, ESRs, Safety Management Plans (SMPs)).
• Where applicable, check the PV&DSS hotline mailbox regularly for reported SAEs and forward messages to the designated DSA/Sr. DSA.
• Assist in the maintenance of files regarding adverse event reporting requirements in all countries.
•  Coordinate shipments of safety documents.
•  Prepare and coordinate safety study files for archiving at completion of projects.
•  Arrange and schedule internal and external meetings/teleconferences.
•  Train and mentor the PV&DSS Support Specialists in their day-to-day activities.
•  Work within the Standard Operating Procedure (SOP) system, including departmental Work Instructions (WIs).
• • Build and maintain good PV&DSS relationships across functional units.
• • Any other duties as assigned by management.

Education/Qualifications:

B. Pharm / M. Pharm / Pharm D / BDS / BHMS / BAMS

Experience Required:

0-6 months experience

Batch Required : Any Batch

Salary Expectations : Best In Industry

NOTE: This Job Is Contract Position for 6 months Only.

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