ResponsibilitiesLead centralized monitoring reviews using platforms such as CluePoints to drive risk identification, signal detection, trend analysis, and structured decision-making across assigned studies. Define, implement, and continuously refine Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs), including thresholds, triggers, and escalation pathways aligned to study critical-to-quality factors. Provide expert input into Study Risk Assessments (SRA) during study start-up and contribute to the development of risk review strategies within the Integrated Data Review Plan (IDRP). Critically evaluate centralized monitoring outputs to distinguish true risk signals from noise, incorporating clinical and operational context to identify root causes and recommend appropriate mitigation actions. Integrate insights from Central Monitors and cross-functional data sources to develop a consolidated and continuously evolving view of study risk. Drive accountability for risk mitigation by ensuring actions are clearly defined, tracked, and followed through to resolution in collaboration with Study Delivery Managers and cross-functional stakeholders. Lead Root Cause Analysis (RCA) for significant or recurring risks and assess the effectiveness of mitigation actions to support corrective and preventive actions (CAPA).Qualification & ExperienceDoctorate degree OR Master’s degree and 8+ years of clinical operations execution experience Preferred Experience: 8+ years work experience in life sciences or medically related field, including 3 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company Experience working in global clinical trial teams (phase 1-3 interventional trials) across multiple geographies

ResponsibilitiesResponsible to work as per cGMP and maintain the compliance requirement Responsible to perform method validation & verification on different technique for E&L related work. Responsible to perform extractable & leachable(s) study for different packaging materials by using different analytical techniques like GC/GC-MS, HPLC/LC-MS, ICP/ICP-MS, IR, UV and other relevant techniques Responsible to perform Identification, Investigation and troubleshooting task. Responsible to perform chemical analysis like, Extraction, Refluxing, Residue on ignition, Centrifuging & Evaporation etc. Instrument knowledge like HPLC, UPLC, pH meter, Osmometer, Zeta Sizer, KF titrator, UV-spectrometer, Balance, etc. Basic knowledge of MS office (Word, Excel & Power point)Qualification & ExpeirenceQualification M.Sc.Experience Tenure : 2- 4 yrs.

ResponsibilitiesTo support for commercial troubleshooting/remediation/Market complaints for Non-Oral manufacturing sites US/EU/Row/Domestic) To support for timely investigation/execution and to resume commercial manufacturing and to meet market/ sales requirement. Executions of assigned DMAIC/DMADV projects. Co?ordination and guidance to CFT for way forward. Review and approval of Investigation protocols and reports and sharing to site to meet compliance To lead Investigations of manufacturing sites which are referred to R & D at level 3 for evaluation and root cause analysis as a part of R &D Central investigation team. To provide technical support, during any stage of commercial manufacturing, as required by site (QC/ QA or Production). Technical support may include, but not limited to, review of CAPA or support for manufacturing site related query response. To collect data on intimation of failure OOS/OOT/Market complaints by site. To review site investigation report, product/method development reports, historical data trending, applying six sigma tools i.e .prioritization tools & technique, and statistical analysis. Planning and execution of investigational hypothesis and generation of analytical data at ADD as part of investigation/hypothesis study. Preparation of technical report of hypothesis study/investigation. Communication and discussion with site for root cause and for suitable CAPA and participation with CFT discussions with sites. Close co-ordination with CIT- ADD , FR&D, ADD Characterization team, manufacturing QA, Operation etc. to meet KPI such as TAT less then 30 days. Prioritization of refer issues from site and conducting meetings for the same. Maintain CIT Tracker and update to leadership weekly. To provide suggestions to manufacturing sites for improvement in process or analytical method to improve product robustness.Qualification & ExpeirenceGraduate : M.Pharm Experience Tenure : Minimum 8 - 12 years of experience

Responsibilities 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.Qualification & ExpeirenceBachelor'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.

ResponsibilitiesPeople: (1) Maintain effective relationship with the end stakeholders (medical scientific community) within the allocated Global Business Unit and product – with an end objective to develop education and communication content as per requirement; (2) Interact effectively with health care professionals on publication content; and (3) Constantly assist junior writers in developing knowledge and sharing expertise Performance: (1) Provide publication/medical education material (slide deck, abstract, poster, manuscript etc.) as per agreed timelines and quality and (2) Provide strategic support with individuals and institutions, which may serve as resources for publications purpose Process: (1) Develop complex publication/medical education material; (2) Support medical communication and develop subject matter expertise for the assigned therapeutic area(s); (3) Assist the assigned scientific communication team in conducting comprehensive publication-need analysis; (4) Implement the publication plan and associated activities for the year identified for the region; (5) Work with selected vendors within the region to deliver the required deliverables as per defined process; (6) Leverage advanced training delivery tools and techniques thereby enhancing the effectiveness of training delivery; and (7) Design an overall plan of action based on end-user feedback and improve course content and delivery Stakeholder: (1) Work closely with scientific communication teams in regions/areas to identify publication need and assist in developing assigned deliverables and (2) Liaise with medical department to prepare relevant and customized deliverables ExperienceExperience: 4+ years of experience in content creation for the pharmaceutical/healthcare industry, or academia Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment 

Responsibilities Sales and Business Development Develop and execute territory business plans to achieve sales targets Conduct face-to-face meetings with healthcare professionals to promote Sanofi products Track and analyze sales performance metrics and market trends Identify new business opportunities within assigned territory Customer Relationship Management Build and maintain strong relationships with healthcare professionals and key decision-makers Record customer interactions and insights in CRM system Respond to customer inquiries and provide product information Collaborate with Key Account Managers on strategic accounts Product Knowledge and Communication Maintain in-depth knowledge of Sanofi products, therapeutic areas, and competitive landscapeQualification & Experience Experience: 2-3 years of sales experience  Soft skills: Communication/presentation skills/ Selling and negotiation skills.  Technical skills: Product knowledge/Market Knowledge/Business Policy Knowledge  Education: B. Sc. Or Preferably B.Pharma

 Responsibilities Sales and Business Development Develop and execute territory business plans to achieve sales targets Conduct face-to-face meetings with healthcare professionals to promote Sanofi products Track and analyze sales performance metrics and market trends Identify new business opportunities within assigned territory Customer Relationship Management Build and maintain strong relationships with healthcare professionals and key decision-makers Record customer interactions and insights in CRM system Respond to customer inquiries and provide product information Collaborate with Key Account Managers on strategic accounts Product Knowledge and CommunicationQualification & Experience Experience: 2-3 years of sales experience  Soft skills: Communication/presentation skills/ Selling and negotiation skills.  Technical skills: Product knowledge/Market Knowledge/Business Policy Knowledge  Education: B. Sc. Or Preferably B.Pharma

Qualification & Experience        EXPERIENCE (in Years) : 1–2 years                ELIGIBILITY : GNM / B.Sc. Nursing + BLS/ACLS certification | Experience: 1–2 years  

Qualification & Experience        EXPERIENCE (in Years) : MBBS (0–1 year experience) OR BAMS/BHMS (0–1 year experience)          ELIGIBILITY : Areas: Ward and casualty  

Qualification & Experience              EXPERIENCE (in Years) : 0-1 years in hospital Pharmacy              ELIGIBILITY : Qualification: B Pharm/D Pharm