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182 Sun Pharmaceutical Industries Jobs
Team Member - Clinical Research
Sun Pharmaceutical Industries
posted 23d ago
Job Role Insights
Flexible timing
Key skills for the job
Job Description
YOUR TASKS AND RESPONSIBILITIES:
CRO Managed Studies:
- Manage Contract Research Organization (CRO) for effective execution of interventional, non-interventional and epidemiological studies
- Identify potential investigators and sites for clinical studies in collaboration with CROs and India Medical Affairs team
- Support in preparation and review of clinical trial documents for Ethics committee (EC) & Drugs Controller General of India (DCGI) and/or other regulatory submission (as applicable)
- Vendor management as per Sun Pharma s applicable policies & procedures
- Coordination with investigator and sites for executing clinical study agreements & financial agreements in co-ordination with CRO
- Coordinate with internal stakeholders (Medical, Regulatory, Quality Assurance etc. ) for timely regulatory submissions
- Plan Investigational Product and other related trial material requisition, procurement, and dispatch
- Ensure timely reporting of Serious Adverse Events (SAEs), Suspected Unexpected Serious Adverse Reactions (SUSAR) to regulatory authorities and reporting of SAEs to all sites and investigators
- Ensure training of CROs on Sun s Pharmacovigilance (PV) practices
In-House Managed Studies:
- Site feasibility, potential investigator identification and development of study budgets for each study
- Finalization of investigators, sites and execution of Confidential Disclosure Agreement (CDA) and study related contracts
- Plan and conduct Investigator s Meeting if needed
- Preparation and submission of study documents for EC permission for respective study across centers
- Work with R&D teams and facilitate Investigational Product (IP) procurement and ensuring streamlined auditable trial supplies to respective sites
- Overseeing & documenting IP dispensing, inventory management & reconciliation
- Site selection, Site initiation, Site monitoring and Site close-out activities
- Investigator and site personnel training on Study protocol, procedures and GCP principles
- Ensure timely recruitment of trial participants and subsequent efficient and effective data management
- Ensure regular site monitoring visits as per plan, source data verification, informed consent form review, case report form review, investigational drug accountability, and adverse event review for completeness, accuracy, consistency, and compliance; identify deficiencies and discrepancies, and provide remedial training and/or initiate corrective action as required
- Ensure timely reporting of SAEs, SUSARs and reporting of SAEs to all sites and investigators in
- alignment with regulations and Sun s PV policies
- Coordinate project meetings and preparation of monitoring visit reports
- Risk identification, analysis and Corrective and Preventive Action (CAPA) for sites not meeting
- expectations as per plan
- Co-ordinate with in-house or CRO partners for data management, statistical analysis & statistical analysis report
- Lead & guide data query resolutions in coordination with sites and data management team
- Management of the trial budget(s) and maintenance of the account
WHO YOU ARE:
- 4-5 years experience in a CRO/Pharma/Biotech organization in clinical trial operations
- Experience in handling large clinical trials with multiple sites for different therapeutic areas
- Thorough Knowledge & experience of remote and risk-based monitoring will be of added value
- Must have experience in handling audits & inspections
- Training in clinical trial methodologies, research design and ICH - GCP
- Thorough knowledge of New Drugs and Clinical Trial Rules, 2019, GCP guidelines, ICMR guidelines 2017 and Drugs and Cosmetic Act regulations pertaining to clinical trials
- Strong academic record with strength in research with knowledge of research methodologies
- Experience of working in matrix business environments preferred
- Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards
Job Location: Sun House, Mumbai (Open for Hybrid working)
Employment Type: Full Time, Permanent
Read full job descriptionPrepare for Team Member roles with real interview advice
Top Sun Pharmaceutical Industries Team Member Interview Questions
Q1. How will you start RS method Development for known drug product?
asked in
Executive interview
Q2. What is peak purity and how it is calculated in hplc?
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Q3. 1 - Which biological indicator use in autoclave validation at the time of RVSEB media cycle i.e. 115 C ?
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Executive interview
What people at Sun Pharmaceutical Industries are saying
Team Member salary at Sun Pharmaceutical Industries
reported by
4
employees
with 6-9
years exp.
₹2.5
L/yr - ₹7
L/yr
37%
more
than the average Team Member
Salary in India
View more details
What Sun Pharmaceutical Industries employees are saying about work life
based on 5.8k employees
Flexible timing
Monday to Saturday
No travel
Day Shift
Sun Pharmaceutical Industries Benefits
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Health Insurance Job Training Free Transport Soft Skill Training
Submitted by Employees
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Sun Pharmaceutical Industries Mumbai Office Location
Mumbai, Maharashtra Office
Headquarter
Sun House, CTS No. 201 B/1,, Western Express Highway, Goregaon East, Mumbai, Maharastra 400063, IN
Mumbai, Maharashtra
400063
400063
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