Job Description

Job Title:

Clinical Research Associate

Business Unit:

Medical Affairs & Clinical Research

Location:

Mumbai

At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

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 investigator.

  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 accounts

Job Requirements

Educational Qualification

Bachelor's or Master's degree in a field related to Science, Healthcare, Clinical Research or Life Sciences like Biology, Pharmacology, Nursing, or a related discipline, and/or Post-graduate Diploma in Clinical Research.

Experience

3–5 years of 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.

COMPETENCY REQUIREMENT

Integrity driven decision making skills

Sound functional knowledge in clinical research and operations

Collaboration and teaming with ability to work in a matrix environment

Strategic thinking & sound analytical skills

Big picture orientation with attention to detail

Sense of urgency & desire to excel

Intellectual curiosity

Self-awareness and adaptability to work in a matrix environment

Result oriented and performance driven

Excellent interpersonal & communication skills to effectively interact with a broad range of audience

 PHYSICAL REQUIREMENTS/WORKING CONDITIONS The role is majority office based but will involve an average 8 to 10 days of travel outside Mumbai.

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification.  It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job.  Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

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