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Role & Responsibilities Study Planning & Coordination Develop and maintain study trackers, dashboards, timelines and operational tools Coordinate logistics for investigator meetings, site communications and trial-related events Support study start-up activities including system access, document readiness and compliance checks Study Execution & Oversight Monitor global enrollment, data flow and quality metrics using dashboards and reports Support and lead assigned RBQM activities including risk assessment and mitigation planning Track study progress and resolve operational issues with Study Delivery Managers and vendors Support global recruitment and retention strategies Stakeholder & Site Engagement Serve as a key point of contact for routine study updates Collaborate with internal teams, CROs, vendors and investigator sites Identify, prioritize and escalate study risks in a timely manner Data, Systems & TMF Management Maintain accurate data in CTMS, eTMF and other clinical systems Support query resolution, reconciliation and data quality checks Ensure TMF inspection readiness and version-controlled documentation Process Improvement Contribute to process optimization, automation and best-practice sharing Support CAPA activities and implementation of lessons learned across studies Qualification Basic Qualifications Bachelor’s degree OR Associate degree with 4 years of clinical execution experience OR High School Diploma/GED with 6 years of clinical execution experience Preferred Qualifications Minimum 2 years of experience in life sciences or medically related field At least 1 year of biopharmaceutical clinical research experience Experience working on global clinical trials Hands-on knowledge of CTMS, eTMF, EDC and Microsoft Office tools Skills Strong understanding of clinical trial operations and compliance TMF filing and regulatory documentation knowledge Excellent coordination, communication and problem-solving skills High attention to detail and data accuracy Ability to work in global cross-functional teamsAbout the Company Amgen is a global biotechnology leader focused on developing innovative medicines that improve the lives of patients worldwide. With a strong commitment to science, quality, and patient safety, Amgen delivers breakthrough therapies across multiple therapeutic areas and supports world-class global clinical research operations.
Role & Responsibilities Conduct post-discharge follow-up teleconsultations Monitor recovery progress and identify early warning signs Assess medication, laboratory, diet and physiotherapy adherence Provide evidence-based clinical guidance (non-prescribing) Escalate high-risk cases to the clinical team Educate patients on lifestyle modifications and self-care practices Coordinate referrals, diagnostic services and allied healthcare support Maintain accurate electronic medical records Collaborate with program managers to improve care delivery models Qualification MBBS (Mandatory) Additional certification in Family Medicine or Public Health is an advantage Experience 2–4 years of clinical practice preferred Family Medicine, Internal Medicine, Emergency or Community Health experience desirable Skills Strong clinical judgment and analytical ability Excellent communication and patient counselling skills Knowledge of post-hospitalization recovery protocols Ability to prevent readmissions through early intervention Familiarity with teleconsultation platforms preferred Benefits Fixed daytime working hours Permanent employment Exposure to digital healthcare and population health programs Career growth in HealthTech and Value-Based Care systemsAbout the Company HEAPS Health Solutions is a health-tech organization headquartered in Bangalore with offices in Mumbai, Hyderabad and Delhi. The company leverages data analytics, artificial intelligence and machine learning to deliver value-based digital healthcare and patient care coordination services.
Role & Responsibilities Assist in reviewing clinical study protocols, ICFs and trial-related documents Identify protocol deviations, inconsistencies and missing data Maintain documentation as per SOPs, GCP and regulatory guidelines Conduct literature searches using PubMed, Google Scholar and other databases Summarize clinical, safety and therapeutic literature Support preparation of literature reviews and study summaries Assist in clinical trial monitoring activities under supervision Review CRFs, essential documents and Trial Master File (TMF) Track study timelines, compliance and site-level activities Coordinate with investigators, clinical sites and internal stakeholders Qualification B.Pharm / M.Pharm / Life Sciences graduate Experience 0 to 1 year (Freshers can apply) Skills Basic knowledge of clinical research and clinical trial processes Understanding of GCP, ICH and regulatory guidelines Good documentation and attention to detail Strong written and verbal communication skills Proficiency in MS Word, Excel and PowerPoint Ability to perform scientific literature search and summarization About the Company A growing clinical research organization offering exposure to real-time clinical trials, regulatory documentation, mentorship and long-term career growth in clinical operations and medical writing
Role & Responsibilities Achieve monthly, quarterly and annual clinical and sales support targets Partner with sales teams to provide intensive clinical support to dental professionals Assist dentists with case assessment, ClinCheck usage, record taking and aligner troubleshooting Review ClinChecks for newly trained and existing doctors Transfer complex cases to senior clinical consultants Prepare and provide clinical materials and documentation to customers Deliver clinical training and field coaching to internal teams, distributors and external customers Provide weekly and monthly clinical feedback reports to Clinical Support Manager – India Coordinate mentorship, smile programs and other clinical marketing initiatives Monitor competitor activities and share market intelligence with marketing team Maintain professional conduct, ethical relationships and quality compliance Plan, organize and manage clinical events and speaker programs Build and develop relationships with certified and non-certified Invisalign providers Support new product launches and continuous staff education Manage quality updates and customer product feedback Open to extensive travel Qualification BDS / DDS (Doctor of Dental Surgery) Experience Minimum 2+ years corporate working experience Prior experience in training dentists / orthodontists preferred Skills Strong clinical orthodontic knowledge Excellent communication and presentation skills Proficiency in English Relationship building and training abilities Organizational, reporting and analytical skills About the Company Align Technology is a global leader in clear aligner and digital orthodontic solutions, best known for Invisalign. The organization focuses on innovation, digital dentistry and clinical education while supporting dental professionals worldwide.
Role & Responsibilities Assess, diagnose and treat orthopedic and sports-related conditions Provide rehabilitation programs for injury recovery and performance improvement Conduct clinical Pilates sessions and functional training Manage pre-natal and post-natal physiotherapy care Develop personalized treatment plans based on patient needs Monitor patient progress and update treatment programs Maintain proper clinical documentation Ensure safe, ethical and professional practice Qualification Bachelor’s or Master’s degree in Physiotherapy Preferably MPT (Orthopedics / Sports) Experience Minimum 1–2 years of clinical experience preferred Skills Orthopedic and sports rehabilitation techniques Clinical Pilates knowledge Pre and post-natal physiotherapy care Patient assessment and communication Documentation and record keeping Professional and empathetic patient handling About the Company A specialty orthopedic and sports rehabilitation centre cum Pilates studio providing advanced rehabilitation, fitness and women-centric physiotherapy services Focused on modern, evidence-based therapy, functional recovery and holistic patient wellness
About Role & Responsibilities • Assist with evidence synthesis and health economics-related tasks • Conduct data analysis and report preparation for clinical studies • Work with cross-functional teams to support decision-making Qualification • M.Pharm, M.Sc, or related discipline / MBBS, MD Experience • 0-2 years of experience in evidence synthesis or related roles Skills • Strong analytical and data interpretation skills • Proficiency in health economics methodologies About the Company Sanofi is a global healthcare leader providing innovative treatments in various therapeutic areas
Lead medical strategy for key therapeutic areas. Experience in clinical trials and regulatory affairs needed. **What you will do:** - Lead daily clinical operations. - Mentor junior staff members. - Participate in quality improvement initiatives. **Requirements:** - Proven experience in the field. - Strong communication skills. - Valid license and registration.
Lead medical strategy for key therapeutic areas. Experience in clinical trials and regulatory affairs needed. **Key Responsibilities:** - Provide high-quality patient care. - Collaborate with cross-functional teams. - Ensure compliance with medical standards. - Maintain accurate patient records. **About the Role:** This is a key position within our growing team. We offer competitive compensation and opportunities for professional development.
Key Responsibilities Lead and govern global PV safety systems, data marts, UAT and system validation Ensure data integrity, compliance, inspection readiness and regulatory reporting (PSUR, DSUR, PADER) Oversee EDC–Safety DB integrations and reporting solutions (QBE, dashboards) Drive automation, AI adoption and PV process innovation Develop SOPs, training programs and mentor teams Support audits, inspections and QPPV-delegated activities Required Skills & Experience Strong experience with Argus / ArisGlobal LifeSphere Knowledge of global PV regulations, SDLC and system validation Reporting tools: Cognos, Spotfire, Tableau; Oracle DB, PL/SQL, Python preferred Pharma / Health Authority experience mandatory Education Doctorate OR Master’s + 3 yrs OR Bachelor’s + 5 yrs OR Associate’s + 10 yrs OR High School + 12 yrs relevant experience
Job ID: 25650 About the Role Execute medical affairs strategy in the assigned zone, driving scientific engagement, medical projects, and regulatory support to strengthen Boehringer Ingelheim’s diabetes portfolio. Key Responsibilities Engage with HCPs, attend scientific forums, and review literature to gather insights on therapy trends Deliver clear, non-promotional scientific communication to internal and external stakeholders Execute medical projects including IIS studies Support medico-marketing strategy implementation Identify and develop relationships with KOLs and expert experts (EEs) Provide medical support for product registrations, new indications, and defense of marketed products Prepare and review labeling and regulatory documentation Support regulatory affairs with expert access Eligibility Medical degree (Pharmacology preferred) or Life Sciences qualification 0–3 years pharma/healthcare experience (Fresh MD Pharmacology graduates can apply) 10+ years field experience acceptable for non-doctoral candidates Strong scientific knowledge in diabetes therapy area Good communication and MS Office skills
About Role & Responsibilities • Lead the medical affairs team to support the development and delivery of innovative medicines • Provide medical expertise in the development of marketing strategies • Collaborate with cross-functional teams to ensure medical alignment and compliance • Manage relationships with KOLs, researchers, and healthcare professionals • Ensure the adherence to regulatory standards and medical guidelines Qualification • Medical degree (MBBS/MD) or PhD in Life Sciences or related field Experience • 5+ years of experience in medical affairs, with leadership experience Skills • Strong leadership and team management skills • In-depth knowledge of medical affairs processes • Excellent communication, presentation, and interpersonal skills About the Company Dr. Reddy's Laboratories is a global pharmaceutical company dedicated to providing affordable and innovative medicines
About Role & Responsibilities • Lead and oversee the medical affairs department's operations • Provide strategic and medical expertise to support business goals • Work closely with cross-functional teams to align on medical strategies • Manage relationships with key opinion leaders (KOLs), regulatory bodies, and healthcare professionals • Ensure regulatory compliance in all medical activities and interactions Qualification • Medical degree (MBBS/MD) or PhD in Life Sciences or related fields Experience • 4+ years of experience in medical affairs with leadership or consultancy roles Skills • Strong leadership and team management skills • Excellent communication and collaboration skills • In-depth understanding of regulatory standards and medical practices About the Company Dr. Reddy's Laboratories is a multinational pharmaceutical company focused on providing high-quality, affordable medicines
About Role & Responsibilities • Assist in the development and implementation of medical affairs strategies • Provide medical expertise for marketing and regulatory submissions • Collaborate with internal teams to ensure medical compliance • Manage KOL relationships and facilitate scientific discussions • Support the preparation of clinical and scientific data for publications and presentations Qualification • Medical degree (MBBS/MD) or PhD in Life Sciences or related fields Experience • 2 – 4 years of experience in medical affairs or related roles Skills • Strong communication and interpersonal skills • Knowledge of regulatory standards and medical guidelines • Ability to work in cross-functional teams About the Company Dr. Reddy's Laboratories is a global pharmaceutical company committed to providing innovative, affordable healthcare solutions
Lead medical strategy for key therapeutic areas. Experience in clinical trials and regulatory affairs needed. **What you will do:** - Lead daily clinical operations. - Mentor junior staff members. - Participate in quality improvement initiatives. **Requirements:** - Proven experience in the field. - Strong communication skills. - Valid license and registration.
Lead medical strategy for key therapeutic areas. Experience in clinical trials and regulatory affairs needed. **What you will do:** - Lead daily clinical operations. - Mentor junior staff members. - Participate in quality improvement initiatives. **Requirements:** - Proven experience in the field. - Strong communication skills. - Valid license and registration.
Lead medical strategy for key therapeutic areas. Experience in clinical trials and regulatory affairs needed. **What you will do:** - Lead daily clinical operations. - Mentor junior staff members. - Participate in quality improvement initiatives. **Requirements:** - Proven experience in the field. - Strong communication skills. - Valid license and registration.
About the role & responsibilities • Act as primary client interface for Safety & Pharmacovigilance services • Lead and manage Safety and PV teams across programs • Oversee delivery as per Safety Management Plans and contracted scope • Monitor quality, KPIs, productivity and drive performance improvement • Ensure timely safety reporting and regulatory compliance • Review study budgets, forecasts and invoicing • Serve as escalation point for sponsors • Lead PV projects and inspections readiness activities • Review protocols, CRFs, SAE forms and safety documents • Develop and approve SOPs, WIs and process improvements • Support business development, bids and proposal reviews • Provide PV training and expert consultation Qualification • Bachelor’s degree in Life Sciences / Pharmacy / Nursing / Healthcare Experience • Extensive leadership experience in Safety & Pharmacovigilance • CRO exposure preferred Skills • ICH-GCP and GVP regulations • Safety reporting operations • People and project management • Budgeting and financial oversight • Strong stakeholder communication About the company • Syneos Health is a global biopharmaceutical solutions organization working on most FDA-approved novel drugs
About the role & responsibilities • Support configuration and optimization of global safety databases • Perform UAT, system validation and safety data integrity checks • Generate and review safety outputs for PSUR, DSUR, PADER, audits and inspections • Configure reports, QBE searches and quality review processes • Support study integrations and EDC–safety database mappings • Drive automation and AI-enabled PV innovations • Develop training, SOPs and support regulatory inspections Qualification • Master’s degree • Bachelor’s degree with relevant PV experience accepted Experience • Pharmaceutical industry / health authority experience mandatory Skills • Argus / LifeSphere safety databases • Aggregate safety reporting (PSUR, DSUR, PADER) • PV analytics and data quality • UAT and system validation • Strong stakeholder communication About the company • Amgen is a global biopharmaceutical leader focused on innovation and patient safety
Lead medical strategy for key therapeutic areas. Experience in clinical trials and regulatory affairs needed. **Key Responsibilities:** - Provide high-quality patient care. - Collaborate with cross-functional teams. - Ensure compliance with medical standards. - Maintain accurate patient records. **About the Role:** This is a key position within our growing team. We offer competitive compensation and opportunities for professional development.
Lead medical strategy for key therapeutic areas. Experience in clinical trials and regulatory affairs needed. **Key Responsibilities:** - Provide high-quality patient care. - Collaborate with cross-functional teams. - Ensure compliance with medical standards. - Maintain accurate patient records. **About the Role:** This is a key position within our growing team. We offer competitive compensation and opportunities for professional development.