Browse the latest opportunities in Hyderabad.
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.
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 • Lead and manage pharmacovigilance safety teams • Oversee ICSR case processing, quality and regulatory compliance • Manage safety projects, deliverables and timelines • Monitor workload distribution, productivity and performance metrics • Review safety budgets, expenses and invoicing • Ensure compliance with GVP, ICH, GCP and global PV regulations • Support audits, inspections and CAPA activities • Review clinical protocols, CRFs, SAE forms and safety documentation • Support SOP development, process improvements and business development Qualification • Bachelor’s degree in Life Sciences / Biological Sciences / Healthcare / Nursing Experience • Minimum 8 years pharmacovigilance experience • Minimum 5 years people management experience • CRO experience preferred Skills • ICSR management and safety project leadership • ARGUS / ARISg Safety database expertise • Advanced MS Excel skills • SQL / Power BI knowledge (preferred) • Strong communication, leadership and client management skills About the company • Syneos Health is a global biopharmaceutical solutions organization operating in 110+ countries, supporting majority of FDA and EMA approved products
About the role & responsibilities • Lead Medical Affairs strategy for oncology portfolio • Provide scientific and ethical oversight for promotional and medical activities • Support marketing & brand strategy with medical inputs • Approve promotional and educational materials • Lead KOL engagement, CMEs, advisory boards and clinical research support • Provide medical training to sales and marketing teams • Support product registration, safety reporting and regulatory documentation • Manage Medical Affairs team and ensure performance and compliance • Support new product planning, launches and business development Qualification • Postgraduate degree in Pharmacology or other Medical specialty • OR Graduate degree in Medicine Experience • 6–8 years Medical Affairs / Medical Advisor experience • Minimum 3 years Oncology therapy area experience • Prior oncology new launch experience required Skills • Oncology therapeutic expertise • Medical writing and presentation skills • Clinical trial knowledge and regulatory understanding • KOL engagement and stakeholder management • Strategic thinking and people management About the company • Dr. Reddy’s Laboratories Ltd is a leading global pharmaceutical company operating in 66+ countries, delivering affordable and innovative medicines worldwide
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 Company • Boehringer Ingelheim is a global, research-driven pharmaceutical company focused on innovative therapies across human and animal health • Strong presence in medical affairs, clinical research, and regulatory compliance worldwide About the Role & Responsibilities • Execute medical affairs strategy and scientific engagement activities • Engage Key Opinion Leaders (KOLs) and Healthcare Professionals (HCPs) • Support medical projects and Investigator Initiated Studies (IIS) • Provide scientific communication and medical education • Support advisory boards, CMEs, and scientific meetings • Provide field-based medical support Qualification • MD preferred (Pharmacology desirable) or Life Sciences degree Skills • Strong scientific communication and presentation skills • Medical affairs and clinical research understanding • KOL and HCP engagement skills • Medical strategy execution capability • Good documentation and reporting Experience • 0–3 years Medical Affairs / Pharma experience • Fresh MD Pharmacology graduates are welcome Salary • Competitive salary package Benefits • Exposure to global medical affairs projects • Career growth opportunities • Continuous learning and development
About the Company • Medifodil Smart Pharma Solutions is a global pharmacovigilance and drug safety organization supporting human and veterinary medicinal products • Works with international pharma and biotech clients to ensure regulatory compliance and safety management About the Role & Responsibilities • Process adverse event cases for veterinary medicinal products • Review and document Individual Case Safety Reports (ICSRs) • Perform medical review, causality assessment, and case follow-ups • Ensure compliance with global and local veterinary PV regulations • Support signal detection, risk management, and regulatory reporting • Maintain accurate documentation in PV safety databases • Collaborate with internal teams to deliver high-quality PV outputs Qualification • BVSc / MVSc (Veterinary Science) Skills • Knowledge of veterinary pharmacovigilance concepts • Understanding of ICSR processing and regulatory guidelines • Good documentation and reporting skills • Strong communication and attention to detail Experience • Freshers welcome • 2+ years of Veterinary PV experience preferred Salary • ₹15,00,000 – ₹24,00,000 per annum Benefits • Hybrid work model • Global project exposure • Professional growth opportunities • Supportive work culture
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. **Job Duties:** - Diagnose and treat patients. - Prescribe medications as necessary. - Order and interpret diagnostic tests. - Advise patients on preventative health. **Benefits:** - Health insurance. - Paid time off. - Continuing education support.
Lead medical strategy for key therapeutic areas. Experience in clinical trials and regulatory affairs needed. **Job Duties:** - Diagnose and treat patients. - Prescribe medications as necessary. - Order and interpret diagnostic tests. - Advise patients on preventative health. **Benefits:** - Health insurance. - Paid time off. - Continuing education support.
Lead medical strategy for key therapeutic areas. Experience in clinical trials and regulatory affairs needed. **Job Duties:** - Diagnose and treat patients. - Prescribe medications as necessary. - Order and interpret diagnostic tests. - Advise patients on preventative health. **Benefits:** - Health insurance. - Paid time off. - Continuing education support.
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.
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.
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.