Tata Institute of Fundamental Research Recruitment 2020 Details
- Application Last Date : 12th January 2021
Roles and Responsibilities
In this role, you are required to solve routine problems, largely through precedent and referral to general guidelines
Your expected interactions are within your team and direct supervisor
You will be provided detailed to a moderate level of instruction on daily work tasks and detailed instruction on new assignments and the decisions that you make that would 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 required to help in the overall team's workload by managing your deliverables and help the team when required
You will be an individual contributor as a part of a team, with a predetermined focused scope of work.
Qualifications
BE/BCA/Bachelor of Pharmacy/Master of Pharmacy/Bachelors of Information Technology
TO APPLY CLICK HERE
Team Lead - CDM/PV
Qualification:
Graduate/Post Graduate/ Doctorate degree in life sciences/Pharmacy/Medical sciences/Registered Nurse
Responsibility:
Business/ Customer:
Minimal Customer interaction under guidance.
Understands Domain Process/sub process, functions, terminologies (such as SOP, QC checklists).
For PV/Complaints Management Individuals in this role perform data entry of data received from Source documents into the respective Clinical/Safety database While peroforming this activity the associate is responsible for meeting turnaround times and accuracy.
These associates are usually used to handle more critical/senitive transactions.
CODING:
(same as PE)
Perform coding activities on the assigned project with timelines and efficiency.
• Import uncoded terms in database and export coded medical terms from coding platform.
• Query Management.
• Create “New Term Request” and prioritize.
• Perform Dictionary upversioning activity as and when required.
CDM:
Performs Migrations / Set up / Close out activities apart from Study Conduct activities under supervision and quality checks from Team Lead.
May do the Peer QC of the TJDA activities.
Generates all study related reports, status updates, and carries out all study related email conversation and communication with internal stakeholders and Client.
Project / Process:
Attempts Complex problems (procedures/processes) and refers to Supervisor/Line Manager in rare cases.
Handle first level processing of transactions.
Adhere to quality requirements, achieve targets/volumes in given TAT(Turn around time).
Proactively identify issues.
Contribute to process improvement initiatives.
Identify and report process changes.
Adhere to the mandatory industry regulation and compliance requirements for the given process.
Knowledge Management:
Update Process documentation as appropriate for the process under guidance.
Participate in knowledge transfer.
People/Team Management:
Adhere to org hygiene and compliance needs in terms of.
a Personal Utilization & Time sheet submission.
b Personal and new hire Assimilation.
c Attendance.
d Team Initiatives.
Collate team performance metrics.
Manage break schedule/transport logistics for the team in the absence of his/her supervisor.
Good To Have Skills
Pharmacovigilance&Safety Ops
PV Case Processing
TO APPLY CLICK HERE
UPSC Vacancy 2020 , Union Public Service Commission (Union Public Service Commission) has published recruitment for NDA & NA (I) Examination posts. The desirous candidate is requested to take all the information before applying in this government employment, only then his eligibility Apply as per Union Public Service Commission Vacancy 2020 , Recruitment Details Complete Union Public Service Commission Job 2020 Vacancy.
Educational Qualification for UPSC :
Even if there is a degree of 12th or its equivalent, it is acceptable to see the published notifications for more information to visits official website.
Total post in UPSC : 400 posts
1. National Defense Academy – 370
2. Naval Academy (10 + 2 Cadet Entry Scheme) – 30 posts.
Important Dates for UPSC :
Job published date: 31-12-2020
Last date for application: 19-01-2021
Age Limit for UPSC :
The age of the candidate should be between the years 02-07-2002 – 01-07-2005. Please see published notification for age relaxation and other information to visits official website.
Selection Process for UPSC :
According to the performance in this Government Job written test, SSB test / interview, the candidate will be selected in employment.
Salary for UPSC :
According to the notification, salary will be as per rules in the published Government Job.
Application Mode for UPSC :
For this employment, you will have to apply online and fill all the useful information by going to the official website.
Application Fees for UPSC :
Gen / OBC / EWS: ₹ 100 / – &
SC / ST / Women: Nil
Apply Online
OFFICIAL SITE
Important Vacancy details:
Note:If interested candidates can share your resume to mentioned mail ID Below.
vijaykumar.y@heterodrugs.com
Job Description: Hiring For Production -Jr.Chemist in Hetero Labs Limited! If interested candidates can share your resume to mentioned mail ID vijaykumar.y@heterodrugs.com

Selection Process: The selection will be on the basis of Interview.
Job Purpose
Develop and review clinical documents for regulated and non-regulated markets ensuring regulatory compliance and thus assisting on-time product registration and renewal
Location: Vikhroli
Education Qualification
B. Pharm/ M. Pharm/ PhD (Pharmacology)/MSc (Clinical research)
Accountabilities
1. Develop and review documents for clinical and bioequivalence studies to align with product strategy and registration
2. Develop and review common technical documents for regulated and non-regulated market as per country specific guidance for timely registration and renewal of dossier
3. Prepare proposals and justification of queries to different regulatory bodies by gathering literature to obtain approvals/waivers for the molecule
4. Prepare and review SOPs and templates to implement standardized systems and document framework to achieve consistent quality and uniformity in documentation
5. Prepare manuscripts/ abstracts for publication by evaluating the studies conducted by Cipla to represent Cipla globally
Relevant Work Experience
B. Pharm with at least 3-4 years of experience in medical and regulatory writing, M. Pharm (Pharmacology), MSc (Clinical research) with at least 2-3 years of experience in medical and regulatory writing. PhD (Pharmacology) with at least 1-2 years of experience in medical and regulatory writing.