ResponsibilitiesCapacity Planning & Capacity Effective Utilization and Mapping of the budget Production planning and scheduling Material planning and scheduling Campaign Planning Master data management Business Continuity – De risking Plan (OS to IH, IH to OS), AVD Plan Implementation Site Transfer- API & Intermediate APO cycle Run: DRP >> NPR>>RCCP >> MRP >> PR review & release. Stock allocation File updating and tracking the D vs C, C vs S. Demand Fidelity (Captive, Filling, Launch & Marketing) NPL, Filling & Query Batches Supply management SCM Process maturity - Norms Setting, Cost to Serve, Planning Master Data Controller Chronic Supply Issues Resolution (Captive & Market) Inventory optimization Data management and support for the S&OP process. Daily / Weekly MIS report review & take necessary action

ResponsibilitiesStrong knowledge of USFDA, ICH guidelines, regional regulations (US, EU, India), and submission formats. Prepare, compile, and submit regulatory dossiers (e.g., CTD/eCTD) for new drug applications (NDAs), ANDAs, MAAs, and post-approval changes Support regulatory strategy development for new products and markets Coordinate with cross-functional teams (CDMO, R&D, Manufacturing) to gather required documentation and data. Respond to queries and deficiency letters from regulatory authorities Maintain regulatory databases and track submission timelines and approvalsQualification & ExperienceGraduate : M.Pharm Experience Tenure : 2- 5 years of relevant experience

Responsibilities Literature search and study designing of Bioavailability and Bioequivalence studies of oral & non-oral products towards different regulatory submission.  Review of BA/BE study protocol and provide Pharmacokinetic (PK) inputs into the study protocols  Coordinate with the CRO in India and outside India for finalizing biostudy pilot and pivotal study protocol for DCGI BE application.  Develop protocol for patient based BA/BE studies & PD end point study for complex generics.  Perform PK and Statistical analysis of in-vivo data obtained from BA/BE and pharmacokinetics studies using Phoenix Software.  Literature search and study designing of Bioavailability and Bioequivalence studies of oral & non-oral products towards different regulatory submission.  Review of BA/BE study protocol and provide Pharmacokinetic (PK) inputs into the study protocols Qualification & ExperienceM.Pharm Experience Tenure : 4-6 years

ResponsibilitiesWorking independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required. Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff. Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.Qualification & ExperienceUniversity degree in medicine, science, or equivalent Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data Excellent written and verbal communication in English Good social skills enabling you to deal with queries in a timely manner Willingness to travel as required (approximately 60%) Oncology studies experience is must

ResponsibilitiesDeveloping and executing validation plans, protocols, and reports for software, systems, and processes to ensure compliance with regulatory requirements. Collaborating with IT, QA, and operational teams to assess validation needs and establish best practices in validation methodologies. Conducting risk assessments and impact analyses to identify potential issues and recommend appropriate validation strategies. Documenting validation activities and maintaining accurate records to support audits and inspections. Providing training and guidance to junior analysts, fostering a culture of quality and compliance within the team.Qualification & ExperienceBachelor's degree in Life Sciences, Engineering, Computer Science, or a related field. Extensive experience in validation activities within the healthcare, pharmaceutical, or clinical research sectors. Strong knowledge of regulatory requirements (e.g., GxP, FDA, EMA) and validation best practices. Excellent analytical and problem-solving skills, with a keen attention to detail and accuracy.

ResponsibilitiesLead and execute complex scientific clinical data review at both trial and program levels. Collaborate closely with SRP/SRS to review data, resolve eDC queries, and ensure data accuracy and completeness. Oversee data flows and Data Management Plans while performing continuous, in-depth data review activities. Contribute to protocol design and provide input into eCRFs and data collection tools. Align data review expectations and timelines with SRP/SRS, GDM, CROs, and cross-functional stakeholders. Define data quality standards, conventions, and ensure timely delivery of all CDM milestones. Develop and maintain key documents such as the Integrated Review Plan, ensuring regulatory compliance. Ensure inspection readiness and actively support audits and health authority inspections. Provide program-level leadership by supporting DMLs in planning, resource allocation, and cross-functional collaboration. Drive quality and continuous improvement by implementing best practices and leading process, system, and tool enhancementsQualification & ExperienceBachelor’s degree in Life Sciences or related field with 5+ years of Clinical Data Management experience, including strong expertise in scientific data review. Solid experience in clinical drug development with deep understanding of data flows, data review processes, and ICH-GCP regulatory requirements. Proven leadership capabilities at study or program level, with experience in stakeholder and resource management. Strong collaboration skills with the ability to work effectively with physicians, scientists, CROs, and global cross-functional teams. Proficiency in eDC and clinical data systems, combined with strong analytical, communication, and problem-solving skills and a quality-driven, continuous improvement mindset.

Qualification & Experience                     Experience: 0-1 Years (Freshers can apply)       Qualifications: MBBS                   

Qualification & ExperienceEligibility Criteria: To assist in the management of patients and provide support to the consultants.Qualification: MBBS Experience: 1-2 Years of experience in 100 + bedded NABH accredited Hospital

ResponsibilitiesAdministering radiopharmaceuticals and medications for patient imaging and therapeutic proceduresProcessing data and enhancing digital images using advanced computer technologyProviding images, data analysis and patient information for diagnostic interpretation or therapeutic proceduresEvaluating images to determine the technical quality and calibration of instrumentationEvaluating new protocolsQualification & ExperienceAble to work accurately and with minimal supervision.Ability to comprehend written instructions given by the related departmental personnel.Ability to plan & organize ones work schedule effectively.Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel.Affinity to work in team.Enthusiasm.

ResponsibilitiesTo attend any new patient (admission) within prescribed time frameTo examine & take a proper history of the patient (If he is in a position to give it on his own) or from his relative.Check any previous records, if available.Charts down all the details in the history sheet.Inform the respective consultant about the admission follow his orders.Instruct the nursing staff about the necessary orders to be carried out.If there’s a transfer in-patient from the ICU. Read the transfer summary/ clinical notes carefully and act accordingly.Inform the respective consultants whenever seems significant.Shift Duty:To take rounds and examine individual patients at least once in every shift and as & when needed. Inform the respective consultant/ Registrars if any new findings.To put the notes in clinical sheet.To enter the relevant details of each and every patient accordingly.Attend rounds with the respective consultants and carry out the necessary changes in the order. Enter them in the treatment sheet.Fill the Medicine Card and Non Drug Order sheetTo instruct the nursing staff about orders and follow them upTo follow up with all the investigations to be seen and trace their results. Note down investigation results in the investigation sheet.To Document Verbal Orders correctly in clinical notes if given by consultants.To respond to emergency calls and to activate code blue if any medical emergency is encountered beyond your control.To identify the critical status of patient and shift him to critical care area in time.Always contact primary consultant if found necessary at any point of time.Qualification & ExperienceAble to work accurately and with minimal supervision.Ability to comprehend written instructions given by the Doctors and the other related departmental personnel.Ability to plan & organize ones work schedule effectively.Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel.Affinity to work in team.Verbal Ability/Communication Skill: Ability to comprehend verbal instructions given by the supervisor or head of the department.To give accurate and tactful explanations to patients. Problem solving/ Decision-makingTo think independently and exercise own judgment in consensus with the supervisor.Enthusiasm.Open-mindedness.