ResponsibilitiesLead the overall product life cycle from conception to launch, aligning product vision with customer needs and business goals, for multiple products. Conduct market research and analysis to identify trends, opportunities, and competitive threats in the life sciences sector. Conduct market research to identify vendors available in this space and analytically decide between build vs. buy. Define (hands-on) and prioritize product requirements, features, and functionalities in collaboration with data management operations teams, engineering, data and other teams. Develop and maintain product roadmaps, ensuring clear communication and alignment across all stakeholders. Monitor and evaluate product performance metrics, adjusting strategies as necessary to achieve success.Qualification & ExperienceBachelor’s degree in engineering, Life Sciences, Health Care, or a related field. Extensive experience working on standard EDC products like Medidata, Veeva, CTMS and other similar systems Knowledge of CDISC, ICH frameworks and keeps track of recent changes and advancements Experience of understanding data concepts for data management systems and Business Intelligence products

Qualification & ExperienceEligibility Criteria:       Exp : Candidate with 5+ Years working experience in NABH Accredited hospital      Qualification: Degree /Diploma in Clinical Research                  

ResponsibilitiesPrepare and manage IPQA shift rosters to ensure adequate coverage across all manufacturing and packing areas. Allocate qualified personnel based on activity criticality, workload, and skill matrix. Ensure no gaps during critical operations and maintain backup planning. Ensure IPQA presence during dispensing, granulation, compression, coating, and packing activities to maintain real-time compliance and control. Ensure proper line clearance before starting any activity. Verify equipment cleanliness, status labeling, and removal of previous product/material. Perform and monitor in-process checks such as weight variation, hardness, thickness, disintegration, and coating parameters as per BMR/BPR and SOP requirements. Conduct real-time and final review of batch documents to ensure completeness, accuracy, and compliance with US FDA expectations. Initiate and review deviations, out-of-specification (OOS), and out-of-trend (OOT) events. Drive root cause analysis and ensure effective CAPA implementation.Monitoring of reject handling on shopfloor. Tracking of in-process samples and ensuring timely release of areas for manufacturing and packing. Identification of opportunity of process and practice improvement on shop floor. Ensure all time compliance at manufacturing, packing and warehouse shop floor. Immediate reporting of observed non-compliance to IPQA In charge/ QA Head.Qualification & ExperienceB. Pharm/ M. Pharm/ M.Sc. With relevant experience in pharma. Must have knowledge of working on the shop floor as an in-process quality assurance. Exposure to various regulatory bodies such as US FDA, EU-GMP, MHRA, TGA Exposure to specific dosage forms like OSD.

ResponsibilitiesWorked in a global environment or part of a global study team, having managed relationships with key stakeholders First-hand experience of vendor management and oversight as well as being the primary point of contact for vendor management activities across the lifecycle of global clinical trials Have experience with direct vendor management & oversight including (but not limited to) IRT/eCOA/Central Labs/Cardiac/ECG/PR&R on a global level Management of vendor performance, quality, compliance, timelines, and budget Experience with vendor?related risk management and tracking, issue escalation, and process improvement. Collaboration with cross?functional teams (e.g., Study Leadership, Data Management, Medical, procurement etc.) Strong communication, negotiation, and stakeholder management skills Knowledge of GxP/ICH guidelines and operational processes within clinical studies Experience with study start?up activities, translating protocol/concept sheet to vendor specifications, collecting documents for submissions, UAT (eCOA, IRT etc.), site readiness, and systems/tools Experience handling multiple vendors in parallel, including how they manage complexity and competing priorities Their personal role in UAT such as identifying issues from both patient and trial operational perspectives. Following up with vendors for resolutions before the go-live date and managing fixes and any re?testing prior to go?live Close-out activity and reconciliation experience; invoice and vendor budget reconciliation oversight is preferrable Audit experience is preferrable Sponsor/CRO/vendor transition studies experience is preferrable Protocol amendment experience.Qualification & Experience     Any lifescience education background Minimum 3–5 years of clinical trial experience as PM / GTM - i.e. to have the chance to face different situations and demonstrate experience CRA experience not counted toward the 3–5 years PM requirement Could consider CRA experience + 2-3 years clinical trial experience as PM / GTM - ensuring CRA experience can be extrapolated to demonstrate relevant skills Global experience is required – understand all CTT roles Exposure to EU Clinical Trial Regulation (CTR) is a plus Procurement background is not aligned with this role

ResponsibilitiesTo attend any new patient (admission) immediately. To 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 out of patient from the ICU. Prepare 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 respond to emergency calls immediately. 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 sheet To instruct the nursing staff about orders and follow them up To 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 activate code blue if any medical emergency is encountered beyond your control. Always contact primary consultant if found necessary at any point of time. To assist/ perform procedures as per instructions Discharges/ LAMA/ Death: Prepare summaries according to the policy Fill the medical certificate of cause of death after discussing with ICU In-charge/ Primary consultant Always inform concerned (MLC Nurse/ Casualty In Charge) in case of MLC Pre Surgical & Post Surgical Patients: To follow pre-operative orders in the treatment sheet. To check whether the consents (Surgical, Anesthesia, etc) for the surgery has been taken from the patient. If not inform the respective person. To get the PAC done. To carry out all the pre-operative orders. Inform the consultant over phone during night shift about patient status who are scheduled for surgery next day. To attend patients complaints. To calm the patients if they are apprehensive. Inform the consultant if needed. General: To attend camps according to the policy. To work as per Policies and procedures of organization. To get the cross referral form filled and call cross consultants according to the policy. Use capital letters for medicines (Generic Names/ Salt) and always put sign, name, date and time with every entry you make. To take care about completeness of records To act accordingly as per communicated by hospital management team

ResponsibilitiesClinical responsibility: Performs triage on incoming patients to become part of the ER’s current load Oversees patient care, treatment, and recovery Participates in research efforts and clinical studies Maintains clinical records in line with regulations and standards Clears patients for discharge or further procedures with specialists Conducts follow-up to monitor patient’s condition Research: Conduct medical research to aid in controlling and curing disease, to investigate new medications, and to develop and test new medical techniques. Be thesis guide for fellows, residents and PhD candidates. Administrative: Coordinate and direct work of nurses, medical technicians and other health care providers. Inform students and staff of types and methods of critical care administration, signs of complications, and emergency methods to counteract reactions. Manage Critical Care services, coordinating them with other medical activities and formulating plans and procedures. Teaching: Must take part in the ongoing teaching activities. Organize and attend workshops, seminars, conferences, CME’s at local, regional and national level.

ResponsibilitiesHandles the sourcing, negotiation, and procurement of medical supplies, equipment, and services. Key roles, such as Purchasing Managers or Officers, ensure cost-effective, timely acquisition of quality products while maintaining inventory levels to support clinical operations.Qualification & ExperienceWork Experience : 1 - 5 Qualification : Any Graduate

Responsibilities  Hands-on data scientist or machine learning engineer that will be expected to ideate, design, develop, model and deploy advanced solutions  Collaborate with stakeholders to define project objectives, formulate data-driven hypotheses and identify KPIs for analysis  Gather, preprocess and explore large-scale structured and unstructured data from diverse sources, including clinical trials, patient records and genetic data  Apply advanced statistical analysis, machine learning algorithms, and predictive modelling techniques to extract insights and develop models that drive actionable recommendations  Conduct exploratory data analysis (EDA) to identify patterns and anomalies in the data and propose solutions to business problems  Develop and implement predictive models (e.g., regression, clustering, time series forecasting) and generative models (e.g. LLMs) to solve complex business challenges  Collaborate with data engineers and IT teams to ensure data availability, quality and reliability for analysis and modeling  Create and present complex analytical findings and insights to both technical and non-technical stakeholders through clear and compelling visualizations, reports and presentations  Stay up-to-date with the latest methodologies and best practices in statistical analysis, machine learning, and the biopharma industry.Qualification & ExperienceWe welcome a master's or Ph.D. in a relevant fields such as Data Science, Statistics, Computer Science or a related discipline. Proven experience (typically 5+ years) in a data science role, preferably within the biopharma or pharmaceutical industry Strong background in statistical analysis, machine learning and predictive modelling techniques Experience in handling and analyzing large-scale structured and unstructured data sets using SQL, NoSQL or similar technologies Demonstrated ability to develop and implement predictive models and machine learning algorithms Experience working with healthcare data, clinical trials, or related domains is highly desirable Solid understanding of the biopharma industry, including regulatory requirements, clinical trial design, and healthcare data sources

ResponsibilitiesSupport the development and maintenance of comprehensive architecture strategies tailored to the needs of managing and transferring clinical trial data, from research and collection to submission. Research and implement innovative data technologies and methodologiesfor Master Data Management and Data Quality (e.g. Reltio, Data Quality checks etc.) Develop and implement data strategies to ensure the accuracy, integrity, and security of clinical data. Provide technical support and guidance to users as needed. Collaborate closely with other DigitalX team members and data professionals to integrate assigned systems or environments with other systems and workflows, ensuring a smooth and controlled flow of data. Support designing scalable architectures to track and maintainproduct data and associated automated jobs. Oversee and support development of APIs, interfaces, and middleware solutions for seamless communication and data exchange between clinical software systems and databases. Lead or take part in projects related to system upgrades, migrations, or new implementations. Liaise with software vendors and service providers to address issues, manage licenses, and support negotiate contracts. Actively participate in or lead Agile activities, including backlog grooming, using Azure DevOps Services. Stay updated on industry guidelines (e.g. IDMP compliance) and advancements to recommend and implement new tools and practices. Responsible for Data Quality (DQ) business rules implementation, DQ Analysis, and DQ Remediation activities. Identify, document and track DQ violations and defects, work with development, data lake teams to resolve issues. Assistorganizations stay ahead of data trends and discover new ways to useproduct data.Quaification & ExperienceBachelor of Science degree in Computer Science, Information Systems, Data Science, or a related field. Minimum of 5 years of relevant experience working in Master Data Management solutions and Data Quality framework within a healthcare industry. Deep understanding of clinical data systems, as well as related environments and tools. Proficient in Reltio data model configuration (Entity types, attributes), matching rules, operational values and survivorship rules, relationships, User Interface, and hierarchies.

ResponsibilitiesPrioritizes, and performs the day-to-day operations of Clinical Transparency or Public Disclosure, ensuring the timely completion, review and approval of registration, updates and results disclosure activities or public disclosure strategy plans and public disclosure tracking mechanisms for studies and assets conducted globally. Makes appropriate decisions regarding the applicability and timing of clinical transparency or public disclosure activities according to national laws, regulations, industry guidance and corporate position. Manages the review and approval process for Clinical Transparency (clinical trial registrations, updates and results disclosures) and related documents (plain language and redacted documents) or public disclosure strategy plans and public disclosure tracking mechanisms, including communication with partner companies or collaborators. Facilitates periodic review of active registrations or public disclosure strategy plans to ensure records are updated or verified as required. Uses appropriate problem solving to determine escalation of issues to management.Qualification & ExperienceBachelor’s Degree, or equivalent experience required. Proficient organizational skills and high attention to detail. Self-directed and motivated, with ability to work without significant direct supervision, asking questions when necessary. Ability to manage multiple tasks and readily switch activities to accommodate priority needs. Proficient computer skills, including experience with MSWord and Excel. Healthcare professional background preferred.2 years pharmaceutical industry experience in writing content for Clinical Transparency purposes. Clinical trials experience including study management, statistics, medical writing and / or data management preferred. Working knowledge of clinical drug development and clinical trial protocols preferred.