Accenture Hiring 2022 Any Graduation  for Junior Drug Safety Associate At Chennai . Accenture Notification full details below..Interested and eligible candidates can Apply Now.

  • Vacancy details:
  • Post Name: Junior Drug Safety Associate
  • Skill required: Pharmacovigilance - Pharmacovigilance and Drug Safety Surveillance
  • Qualification: Any Graduation  
  • Experienced:0 to 1 years

Job Description: Accenture Hiring For SJunior Drug Safety Associate ! 

  • Important Details :
  • Location: Chennai
  • Post of date: 01/03/2022
  • Selection Process: The selection will be on the basis of Interview.

What would you do?

You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life – enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.

You will be part of a dynamic Pharmacovigilance team with array of capabilities ranging from detection, assessment, understanding and prevention of adverse effects or any other medicine/vaccine related problem following Good Pharmacovigilance Practice (GVP) per client SOPs and applicable global regulatory requirements (Individual Case Safety Reports) to working on various aspects of Aggregate reports such as planning, authoring, reviewing  and publishing of PBRER, PSUR, DSUR, PADER, Addendum to clinical overview (AdCO), Risk Management Plan (RMP), Signal detection and validation reports (SDVR), Cosmetovigilance Safety Reports (CoSR). The Pharmacovigilance team is also responsible for authoring and reviewing clinical documents such Protocols and amendment, Investigator Brochure, Clinical Study Reports (CSR), Synoptic/Abbreviated CSR, Safety Narratives, Clinical Overview/abbreviated Clinical Overview.

In this role, you will be expected to create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements.

What are we looking for?

We are looking for individuals who have the following skillset:
  • Ability to establish strong client relationship
  • Ability to work well in a team
  • Ability to manage multiple stakeholders
  • Ability to meet deadlines

Roles and Responsibilities

    • In this role, you are required to solve routine problems, largely through precedent and referral to general guidelines
    • Your primary interaction is within your team and your direct supervisor
    • You will be given detailed instructions on all tasks that need to be carried out, and the decisions that you make will impact your work
    • You will need to be well versed with basic statistics and terms involved in the day to day business and use it while discussing with stakeholders
    • You will be working closely with project members to effectively deliver on the requirements
    • You will be an individual contributor as a part of a team with a predetermined focused scope of work.

Please note this role may require you to work in rotational shifts.

How to Apply :

Step 1: Click on below link and you will be redirected to  Career Page of Recruiting Company or Career portal.

Step 2. Register on Career Page of the Company or  Career Portal by giving log in credentials and other personal or education details .

Step 3.Upon successful registration .User need to log in with credentials.

Step 4.Once logged in, User need to fill the all relevant personal ,educational  , Work experience details ,attach resume and submit application form.

Click here for notification and Apply