LABCORP – Fresher safety Science analyst Jobs at Bangalore

Labcorp Is Hiring.

openings in Labcorp for candidates having relevant exp (0-5) years in

Pharmacovigilance. Safety science analyst (freshers)

safety science specialist (3-4 years)

safety science coordinator 1 (1-2 years)

safety science coordinator 2 (2-3 years)

senior safety science specialist (4-5


Interested candidates can send me

their resume on my personal email mentioning their relevant exp and domain, I’ll screen to check if those are eligible and mathces with the opening

Safety Science Specialist: Individuals with 3 to 4 years of relevant pharmacovigilance experience.

Send Your Updated Resume to LABCORP HR Team Mail Id

2) Labcorp Drug development hiring Details 2021

Job Name – Safety Science Analyst

Location Bangalore, India

Education/ Qualification

  • Masters in Pharmacy/ Doctrate in Pharma
  • Experience – 0-6 months ( Freshers )
  • Attention to detail
  • Team player.
  • Solid written and verbal communication skills
  • Accurate math and spelling skills preferably with an aptitude for handling and proof reading numerical data
  • Knowledge of MS office Windows applications beneficial
  • Ability to operate standard office equipment.

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
  • assist with the reporting of ESRS to clients, regulatory authorities, ethics committees, investigators and
  • Labcorp Drug Development project personnel, if required, within study specified timelines

Provide administrative support to PV&DSS personnel (e.g word processing, 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)

•Where applicable, check the PV&DSS hotline malbox regularly for reported SAEs and forward messages to thedesignated DSA)/Sr. DSA

• Assist in the maintenance of files regarding adverse event reporting requirements in all countries.

• Maintain and distribute a weekly schedule for PVBDSS staff

• Work within the Standard Operating Procedure (SOP) system, including departmental Work instructions (Wis)

• Build and maintain good PVBDSS relationships across functional units.

• Ensure submission of client related documents is sent to the client within designated time frames (eg SAE reports, ESRS, Safety Management Plans (SMP))

• Assist the DSA/Sr. DSA in preparation of materials needed for client and/or investigator meetings Any other duties as assigned by management.

Application Link –