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

Responsibilities• Achieve assigned activity goals and targets for the territory as agreed with the reporting manager. • Within a specific geographical territory, identify target customers and physician profiling while maintaining and analyzing customer records. • Conduct sales interviews, carry out pre-call planning and preparation and develop a self analytical approach in order to identify learning areas from each call. • Successfully manage objections and/or issues raised, escalating more sensitive or complex queries. • Maintain records in the reporting systems within the required timescales. • Effectively utilize the relevant software (e.g. Electronic Territory Management System, CRM systems) to maintain records updated and to report daily calls • Organize and conduct group events to optimize business while complying with relevant country legislation. • Keep Line Manager informed about changes in competitor activities and other market changes. • Maintain an up-to-date sales / technical knowledge of specialty and disease areas and relevant publications as per customer profile. • Keep all Company equipment safe and in a good state of repair. • Share experiences, ideas and techniques in order to assist with the sales training of colleagues. • Discuss, agree and document assigned activity, Key Performance Indicator tools, and targets as agreed with Line Manager. • Successfully complete career development courses and additional training as required by the customer. • Ensure the reporting of any identified Adverse Events in line with prevailing process and guidelines. • Project a professional impression of the Company and act in accordance with the relevant Pharmaceutical Industry’s Code of Practice • Perform other duties as assigned.Qualification & Experience     • Bachelor's Degree Life Sciences or related field Req • 1 year’s relevant experience Req Or • Equivalent combination of education, training and experience. Req • Good understanding of Pharma Market and related procedures. • Fluency software operating systems, such as MS Office and customer relationship management systems. • Effective verbal and written communication skills. • Strong product knowledge. • Ability to conduct face to face presentations to customers. • Ability to organize and prioritize own workload. • Ability to establish and maintain effective working relationships with coworkers, managers and clients. • Possession of any required industry qualification essential to function as a Medical Representative in the relevant market. Req • AZDL - Driver Licence - Valid And In State Req

Qualification & Experience             Qualification: MD / DNB Paediatrics, DM or Fellowship in Neonatology                 Experience: Minimum 2 years           

Qualification & Experience     Qualification: MBBS  Experience: Fresher's Can Also Apply          Gender: Male / Female        

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.

ResponsibilitiesCheck and ensure with the operating surgeon about his need for standard and special equipment Coordinate with operation theater nurses and Senior Technician to fill the requirements and needs for a particular surgery Liaise with Biomedical Engineer to ensure to smooth functioning of all electrical equipment such as OT lights, OT bed, cautery, ligasure, harmonic, etc Ensure all equipment such as lap monitors are functioning as per requirements Adhere to the Surgical Safety Check list prior to every operation Support in transferring and positioning of the patient prior and after surgeryQualification & Experience    2 years’ + experience post diploma in OT assistance Higher Secondary or Graduation with Diploma / certificate in OT assistance

ResponsibilitiesAggregate Safety Reports & Documentation: Independently lead the preparation/update of complex scheduled and unscheduled aggregate safety reports across multiple product types and regulatory regions, including but not limited to Periodic Safety Update Reports (PSURs), Periodic Benefit Risk Evaluation Reports (PBRERs), United States Periodic Adverse Drug Experience Reports (PADERs), Development Safety Update Reports (DSURs), Addendum to Clinical Overviews (ACOs), Investigational New Drug Annual Report (INDARs), Semi-Annual Safety Reports (SASRs), Annual Risk- Benefit Evaluation (ARBE) report , Safety statements, Health Hazard Evaluation (HHE), Clinical Overview (CO) and any other ad hoc safety documents, ensuring scientific accuracy, regulatory compliance, and timely delivery. Serves as an SME for safety reports, developing templates, guiding teams, and creating strategies to address complex regulatory and data presentation challenges. Facilitate operational coordination, including scheduling and leading meetings, drafting agendas and minutes, tracking action items, and ensuring timely follow-up on open issues to support seamless project execution. Ensure compliance and quality across aggregate safety reports, performing detailed reviews for factual accuracy and internal consistency across documents such as but not limited to PBRERs, DSUR etc.). Manage the distribution of final reports to stakeholders, including partners, affiliates, and health authorities, in accordance with agreed timelines, distribution lists, and email templates (as required). Safety Analysis & Signal Management: Leads advanced safety signal detection and management for key products, integrating diverse data sources and innovative analytical approaches to identify emerging safety concerns. Provides expert interpretation of complex safety data patterns and trends across product lifecycles. Leads clinical safety activities for complex molecules, contributing to strategic decisions as part of the global safety team. Collaborates with cross-functional teams to analyze complex safety data and provide support as part of the study management team. Directs literature review strategies and critically evaluates scientific evidence for inclusion in safety documents. Leads safety evaluations for complex molecules and sensitive indications, providing scientific direction that supports clinical strategy and strengthens regulatory positioning through high-quality safety reports and responses. Qualification & Experience    Preferred qualifications include a university degree in Life Sciences, Health, or Biomedical Sciences—such as Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, Dentistry, or Physiotherapy etc. Or equivalent combination of training and work experience. Clinical exposure in hospital-based environments is considered advantageous.Strong analytical and problem-solving abilities, with the capability to independently evaluate complex data and draw meaningful conclusions. Exceptional communication skills, both verbal and written, including the ability to produce clear, concise, and accurate medical/scientific content. Excellent interpersonal and collaboration skills, fostering productive relationships with clients, cross-functional teams, and stakeholders. Effective organizational and prioritization skills, with the ability to manage multiple tasks enthusiastically and maintain attention to detail under tight timelines. Client-focused mindset, demonstrating flexibility, professionalism, and a proactive approach to meeting client expectations and expanding business opportunities. Strong negotiation and stakeholder management skills, ensuring alignment of resources, timelines, and deliverables across teams and departments. Cultural awareness and adaptability, enabling effective communication and collaboration in global, multicultural environments. Proficient in computer operations and IT tools, with expertise in web-based applications and familiarity with the Windows operating system and Microsoft Office suite (Word, Excel, PowerPoint). Knowledge and Experience: Prior experience in pharmacovigilance, or related fields is preferred. Demonstrates Solid understanding of global pharmacovigilance regulations, medical terminology, and safety-related concepts.:

ResponsibilitiesAggregate Safety Reports & Documentation: Leads the preparation of complex scheduled and unscheduled aggregate safety reports across multiple product types and regulatory regions, including but not limited to Periodic Safety Update Reports (PSURs), Periodic Benefit Risk Evaluation Reports (PBRERs), Periodic Adverse Drug Experience Reports (PADERs), Development Safety Update Reports (DSURs), Addendum to Clinical Overviews (ACOs), Investigational New Drug Annual Report (INDARs), Semi-Annual Safety Reports (SASRs), Annual Risk- Benefit Evaluation (ARBE) report , Safety statements, Health Hazard Evaluation (HHE), Clinical Overview (CO) Develops strategic approaches for challenging safety submissions, incorporating innovative data presentation techniques to enhance clarity and regulatory impact. Reviews and approves high-complexity safety documents, ensuring scientific accuracy, regulatory compliance, and alignment with product strategy. Coordinates multi-document submissions, ensuring consistency and integration across safety documentation packages. Provides expert guidance on evolving global regulatory requirements and advises on their implications for safety documentation. Manages meeting logistics including scheduling, agenda drafting, minute preparation, and tracking of action items, ensuring timely follow-up and resolution of open issues. Safety Analysis & Signal Management:Designs and implements advanced signal detection plans tailored to specific product profiles and diverse data sources. Leads signal detection for priority products by conducting expert-level analyses to uncover subtle safety signals and complex data patterns. Develops robust literature review strategies and critically evaluates complex scientific evidence or inclusion in PSRs, drug safety reports, and RMPs. Supports clinical safety and ad-hoc safety activities for complex molecules, contributing to strategic safety evaluations. Authors and reviews high-priority signal assessment reports and health authority response documents, resolves data challenges, and enhances decision-making through expert analysis and innovative visualizations. Risk Management Plan:Leads the preparation, updating, and integration of Risk Management Plans (RMPs) and Company Core-RMPs (CC-RMPs) across multiple regulatory regions and product types, ensuring alignment with evolving safety profiles and strategic objectives. Prepares and handles reviews of health authority response documents, incorporating safety data and regulatory insights to address queries and support submissions of RMPs. Oversees Reference member state (RMS) updates, ensuring consistency with client conventions, global regulatory expectations, and internal SOPs. Provides strategic input on risk minimization measures and benefit-risk communication, tailoring content to diverse regulatory audiences. Collaborates with cross-functional teams to ensure RMPs are scientifically robust, compliant, and aligned with the overall safety strategy. Qualification & Experience    Preferred qualifications include a university degree in Life Sciences, Health, or Biomedical Sciences—such as Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, Dentistry, or Physiotherapy etc or equivalent combination of training and work experience. Clinical exposure in hospital-based environments is considered advantageous. Demonstrates advanced analytical thinking and problem-solving skills to interpret complex safety data and derive meaningful conclusions to support benefit-risk assessments. Possesses strong scientific writing and communication capabilities, ensuring the production of clear, accurate, and regulatory-compliant documents. Strong capability to lead and collaborate across cross-functional, global teams and build trusted client relationships. Excels in organizational and time management, with the ability to prioritize tasks, manage multiple high-impact projects, and consistently meet deadlines. Proficient in medical writing tools and MS Office applications, with working knowledge of pharmacovigilance databases and coding dictionaries such as MedDRA and WHO-DD. Proactive in adopting new technologies, driving process improvements, and applying innovative approaches to safety documentation. Knowledge and Experience: Prior experience in pharmacovigilance, or related fields is preferred. Demonstrates Solid understanding of global pharmacovigilance regulations, medical terminology, and safety-related concepts.

ResponsibilitiesGeneral Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and global drug safety regulations and guidelines Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting Communicating and discussing issues related to review process with Line Manager/ Project Leader/Designee Interacting with internal and external stakeholders for resolving issues under guidance of senior physicians. Attending and/ or presenting at client/cross functional meetings along with other stakeholders under guidance of senior physicians. Developing knowledge of global regulatory requirements and reporting obligations Case report medical review (as applicable) Performing medical review of cases not limited to (including non-serious and serious spontaneous (including legal cases), clinical trial, and literature cases including combination products {drug-device) according to established client/Parexel Standard Operating Procedures (SOPs; as applicable) and liaising with the client under supervision Writing Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assessing company causality Review appropriateness of medical content in narrative for medical coherence Assessing seriousness, listedness / expectedness of reported events. Providing medical inputs to case processing team Raising appropriate follow-up queries for relevant information from the reporter/HCP (Health Care Professional) Review and verify appropriate selection of adverse events from source documents, assign appropriate Medical Dictionary for Regulatory Activities (MedDRA) code, review narrative Identify and resolve case issues, coordinate with client therapeutic/legal team under supervisionQualification & Experience    Bachelor of Medicine, Bachelor of Surgery (MBBS) / Doctor of Medicine (MD)/ Medically qualified from an acknowledged Medical SchoolCompletion of at least basic training in clinical medicine (residency, internship etc.)Experience in clinical medicine (general or specialist qualifications) which is expected to be kept up to date Ability to work within defined procedures and practices to determine appropriate action Developing knowledge of drug safety, clinical trial and pharmacovigilance principles Good presentation and verbal/written communication skills. Demonstrates potential for technical proficiency, scientific creativity, and collaboration Computer proficiency, ability to work with web-based applications and familiarity with the Windows operating system and Microsoft Office apps. A flexible attitude with respect to work assignments and new learnings. Good understanding of international drug regulation including ICH GCP, GVP, and all other applicable regulations and guidelines. Knowledge and Experience: Experience in pharmacovigilance and medical data review activities is desirable but not essential Good knowledge/understanding of medical terminology. Fresher/ relevant experience in pharmacovigilance/ Drug Safety/clinical practice.

ResponsibilitiesExplain the patient and patient attendants about the present diet recommended as per the medical condition. Resolve patient complaints and act on feedbacks pertaining to nutrition in a timely manner. Counsel and plan diets for the OPD patients. Plan diets for patients in coordination with the Clinical team Approve patients’ meals after evaluating for taste, texture, appearance and temperature of the food.Qualification & Experience    Dietician 2-3 years of experience in the hospital sector Post Graduate Diploma / Masters in Food Nutrition and Dietetics from a reputed university