Doctor Jobs

Role & Responsibilities • Perform quality control (QC) of pharmacovigilance cases • Conduct medical evaluation of adverse event reports • Enter vigilance case data into agreed databases and formats • Perform follow-up of cases via phone and email • Pre-analyse complex cases prior to data entry • Evaluate cases for medical coding as per applicable dictionaries • Assess causality between suspect product and reported events • Determine seriousness and expectedness of events • Identify regulatory submission requirements for each case • Validate documents prepared by Vigilance Associates or Data Managers • Close vigilance case files in compliance with timelines • Support setup and review of ICSR / MLM filters • Analyse inclusion or exclusion of EV / MHRA cases • Provide medical input to the Medical Information division • Support client-specific pharmacovigilance activities within the business unit Qualification • Doctor (MBBS or equivalent) or Pharmacist by training Experience • Minimum 3 years’ experience with service providers in pharmacovigilance • Hands-on experience in QC of safety cases • Experience with SafetyEasy database (mandatory) Skills • Strong knowledge of global pharmacovigilance regulations • Experience working with safety databases • Process-oriented and detail-focused approach • Ability to multitask and manage multiple priorities • Proficiency in Microsoft Office tools • Excellent written and verbal communication skills in English • Strong teamwork and collaboration skills • Flexible and adaptable in a dynamic environment About the Company • ProductLife Group is a global life sciences consulting and services company , Supports pharmaceutical, biotech, and medical device companies across the product lifecycle.

Role & Responsibilities • Provide and supervise comprehensive medical care to people in prison • Deliver, monitor, and evaluate medical programs and healthcare services • Coordinate clinical hours and on-call duties with the Health Services Manager and Director, Medical Services • Work collaboratively within a multidisciplinary healthcare team • Maintain high standards of clinical governance and quality care • Operate effectively within a secure correctional healthcare environment Qualification • Medical Practitioner registered with the Medical Board of Australia (from 1 July 2010) • Documentary evidence of current medical indemnity insurance Experience • Minimum 5 years post-graduate clinical experience • Experience in mental health, drug and alcohol, and emergency care (desirable) • Demonstrated ability to deliver high-quality patient-centred care Skills • Strong written and verbal communication skills • Ability to work effectively within multidisciplinary teams • Sound clinical judgement and professional accountability • Computer literacy relevant to clinical documentation and reporting • Commitment to ongoing professional development About the Company • GEO Healthcare delivers primary and related health services in Victorian men’s public prisons , Subsidiary of The GEO Group Australia Pty Ltd with over 30 years of experience.

Role & Responsibilities • Promote company’s therapy-focused pharmaceutical products to specialist doctors • Develop strong scientific engagement and long-term professional relationships with consultants • Conduct effective product detailing with strong clinical knowledge • Organize CMEs, RTMs, and scientific promotional activities • Achieve therapy-wise prescription generation and sales targets • Monitor competitor brands and market trends in the therapy segment • Ensure product availability at hospitals and key pharmacies • Maintain daily call reports, doctor data, and sales records Qualification • B.Sc (Biology) / B.Pharm Experience • Minimum 1–2 years of pharmaceutical field sales experience • Experience in specialty/therapy segment preferred Skills • Strong therapy and product knowledge • Scientific communication ability • Relationship building with specialist doctors • Target-oriented approach • Good presentation and interpersonal skills About Company Unifaith Biotech Private Limited is a growing pharmaceutical company focused on delivering quality healthcare solutions. The company emphasizes scientific promotion, strong doctor relationships, and expanding its presence in specialized therapy segments.

Roles & Responsibilities:• Deliver comprehensive clinical onboarding, training, and implementation support to dental professionals on SureSmile aligner workflows• Assist clinicians with case selection, treatment planning guidance, and troubleshooting throughout aligner therapy• Conduct chairside and virtual training sessions to ensure smooth adoption of SureSmile in clinical practice• Collaborate with sales and product teams to drive clinical conversions and support practice growth• Build and maintain strong professional relationships with clinicians to ensure satisfaction and protocol adherence• Support and facilitate workshops, webinars, and regional clinical education programsQualifications:• BDS or MDS with specialization or substantial experience in Orthodontics (mandatory)• Strong hands-on knowledge of aligner therapy, digital workflows, and core orthodontic principlesExperience:• Clinical experience in orthodontics and aligner-based treatments preferred• Experience in clinical training, implementation, or education roles is an advantageSkills Required:• Strong understanding of aligner systems and digital orthodontics• Experience with CAD/CAM systems, dental software, or digital dentistry platforms preferred• Excellent communication and presentation skills• Ability to train, educate, and support clinicians effectively• Strong interpersonal and relationship-building abilities• Professional, proactive, and performance-driven approachAbout the Company:Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with over 130 years of innovation. The company develops, manufactures, and markets comprehensive dental and oral healthcare solutions, empowering dental professionals worldwide to deliver safer, more effective, and advanced patient care.

MBBS Doctors

Lead cross-functional medical programs to ensure clinical and scientific support for products. Engage healthcare professionals, support clinical trials, and disseminate medical data. Requires coordination of medical education, compliance, and real-world evidence generation.

About the Role: Johnson & Johnson is seeking an accomplished Associate Director, Global Medical Affairs to lead scientific strategy and medical excellence across its global portfolio. This role is pivotal in shaping evidence generation, scientific communication, and external engagement to advance patient outcomes worldwide. The successful candidate will collaborate closely with cross-functional teams and serve as a scientific leader and strategic partner within the organization. Key Responsibilities: Develop and execute comprehensive global medical affairs strategies for assigned products or therapeutic areas. Lead scientific communication planning, including publications, congresses, and medical education initiatives. Provide medical insights to R&D teams and support global clinical development and evidence-generation activities. Establish and maintain relationships with global Key Opinion Leaders (KOLs) and external scientific experts. Guide real-world evidence (RWE) programs, post-marketing studies, and other data-generation initiatives. Represent medical affairs at advisory boards, congresses, and cross-functional strategic meetings. Ensure adherence to global medical, ethical, and regulatory standards in all medical affairs activities. Qualifications: Advanced degree (MD, PharmD, PhD, or equivalent) is required. 8–12 years of experience in Medical Affairs or related roles in pharmaceutical or biotech industries. Strong expertise in medical strategy, evidence generation, and scientific communications. Proven leadership experience within a global/matrix organizational structure. Excellent communication, stakeholder management, and analytical skills. Why Johnson & Johnson: Opportunity to influence patient outcomes on a global scale. Collaborative and innovative work environment. Professional growth and leadership development opportunities.

About the Role The Medical Affairs Specialist will support Roche’s medical strategy by providing scientific expertise, engaging with healthcare professionals, ensuring compliant dissemination of medical information, and contributing to evidence generation activities. This role plays a key part in aligning medical insights with business objectives and improving patient outcomes across therapeutic areas. Key Responsibilities Scientific & Medical Expertise Provide accurate, balanced, and up-to-date scientific information to internal teams and external stakeholders. Support the development and review of medical/scientific materials, including slide decks, publications, and promotional content. Maintain deep knowledge of assigned therapeutic areas, clinical data, competitors, and market trends. Medical Insights & Stakeholder Engagement Build trusted relationships with Key Opinion Leaders (KOLs), clinicians, and scientific communities. Capture and communicate medical insights to shape Roche’s medical strategies and evidence-generation plans. Support advisory boards, scientific meetings, and investigator-initiated studies. Evidence Generation & Medical Governance Assist in planning and executing local clinical studies, real-world evidence projects, and post-marketing surveillance. Ensure scientific accuracy and compliance with local/global regulatory, legal, and ethical standards. Support pharmacovigilance teams with medical evaluation and safety reporting when required. Cross-Functional Collaboration Partner with commercial, regulatory, market access, and marketing teams to ensure medically sound strategies. Provide medical training to internal teams, including sales and field force, to enhance scientific competency. Contribute to launch readiness, disease education programs, and patient support initiatives. Qualifications & Experience Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine (MBBS/MD preferred). 2–5 years of experience in Medical Affairs, Clinical Research, or related pharmaceutical industry roles. Strong understanding of clinical trials, medical governance, and scientific communication. Excellent communication, analytical, and stakeholder management skills. Ability to work in a fast-paced, matrixed environment and manage multiple priorities. Why Join Roche? Work in a globally respected healthcare company committed to innovation and patient-centricity. Opportunity to collaborate with world-class medical professionals and access cutting-edge scientific resources. Inclusive work environment with strong career development pathways.

Role Overview Responsible for driving medical strategy, providing scientific leadership, and supporting AstraZeneca’s therapeutic areas through evidence-based medical activities, stakeholder engagement, and compliance-driven execution. Key Responsibilities Develop and implement medical plans aligned with global/regional strategies. Serve as scientific expert and deliver accurate, balanced medical information. Engage and build strong relationships with KOLs and external HCPs. Support clinical trials: feasibility, protocol review, and execution. Lead medical reviews of promotional and non-promotional materials. Provide medical training to internal teams and support product launches. Ensure strict compliance with regulatory, ethical, and AstraZeneca governance standards. Skills & Competencies Strong clinical and scientific knowledge. Excellent communication and presentation skills. Ability to interpret scientific data and provide actionable insights. Collaborative mindset with high ethical standards. Qualifications MBBS/MD required. 2–5 years in Medical Affairs or relevant clinical/scientific roles preferred.

Role Overview: Lead Bayer India’s Medical Affairs function, shaping scientific strategy, driving evidence generation, and strengthening external medical engagement across the Pharmaceuticals portfolio. Responsible for medical excellence, compliance, and cross-functional partnership to support patient outcomes and business growth. Key Responsibilities: Develop and execute national Medical Affairs strategy aligned with global/regional plans. Provide scientific leadership for launches, lifecycle management, and evidence-generation (IITs, RWE, Phase IV). Lead KOL engagement, advisory boards, medical education, and scientific communications. Oversee medical review, governance, and regulatory-compliant scientific exchange. Partner with Commercial, Market Access, Regulatory, and PV to shape brand plans and market strategy. Lead, coach, and develop medical managers and MSL teams. Qualifications: MBBS/MD with 12–18+ years of Medical Affairs experience in pharma MNCs. Strong expertise in scientific strategy, clinical research, compliance, and stakeholder management. Proven leadership skills with high scientific, ethical, and strategic acumen.

Remote design work

Python backend development

Data analysis role

Marketing role

Another marketing role

Roles & Responsibilities: • Develop and implement sales strategies for assigned territory to achieve monthly, quarterly, and annual targets. • Promote company products ethically through science-based discussions with doctors, chemists, and other stakeholders. • Organize CMEs, retail meets, market blitzes, and other promotional activities as per division strategy. • Plan and execute merchandising, sampling, and brand visibility activities across clinics and trade. • Facilitate new product launches by identifying and targeting customers, ensuring proper engagement, and providing feedback. • Maintain and update customer and distributor databases; ensure 100% doctor coverage and regular customer interactions. • Monitor prescriptions for Abbott and competitor brands; collect market intelligence and retailer-level inventory data. • Manage distributor network including appointment, credit assessment, stock & sales statement tracking, and claim settlement. • Lead, mentor, and set example for junior team members in adherence to Abbott Code of Business Conduct, FCPA, and pharmacovigilance. • Ensure compliance with company financial, administrative, statutory, and regulatory systems. • Promote Abbott’s values—Pioneering, Achieving, Caring, Enduring—and ensure high-level customer service. • Participate in strategy meetings, workshops, training programs, and other company initiatives to drive performance and brand image. • Adhere to EHS policies, complete required trainings, wear safety gear, report incidents, and contribute to safety improvements. Qualification: • Graduate degree in Life Sciences, Pharmacy, or relevant field. Experience: • Relevant experience in pharmaceutical sales, brand management, or territory management preferred. Skills: • Strong communication, negotiation, and customer relationship management. • Strategic thinking and ability to execute business plans effectively. • Leadership and team mentoring capabilities. • Analytical skills for market intelligence, sales monitoring, and decision-making. • Knowledge of compliance, pharmacovigilance, and ethical promotional practices. About the Organisation: Abbott is a global healthcare company committed to improving lives through innovative medicines, diagnostics, and medical devices. The company emphasizes ethical practices, patient safety, and professional development while fostering a culture of care, innovation, and excellence.

Roles & Responsibilities: • Develop global regulatory project plans for moderate-to-high complexity submissions (CTA/IND, MAA/NDA/BLA, HA meetings/Scientific Advice). • Track regulatory deliverables, ensuring timely submission and life cycle management of products. • Collaborate with Global Regulatory Lead, Regulatory Affairs Manager, and Submission Manager to execute submissions. • Orchestrate Submission Task Force activities, manage risks, interdependencies, and resolve issues impacting timelines. • Set up hypercare for critical submissions to Health Authorities. • Consolidate budget planning and track actuals for regulatory projects; coordinate with project controllers and global project management. • Support operational aspects of in-licensing/out-licensing deals, including asset transfer planning and internal activity initiation. • Improve project management tools, templates, and ensure compliance with Health Authority requirements. • Maintain strong collaboration across cross-functional teams and matrix organization stakeholders. • Ensure documentation and dossier readiness, including CPPs, GMP Certificates, MLs, AtOs, AFs, CLs, PoAs, and legalization frameworks. • Manage regulatory affairs knowledge for post-approval changes, dossier types, and main global procedures. Qualification: • Degree in Life Sciences, Medicine, Pharmacy, PharmD, or related discipline (minimum MSc or equivalent; PhD preferred). • Advanced training in portfolio and project management preferred. Experience: • 8–14 years of work experience in pharmaceutical, regulatory authority, or R&D environments. • Minimum 6–8 years in regulatory affairs or regulatory project management. • Hands-on experience with global regulatory submissions and life cycle management. • Contributor-level experience with RIM and EDMS RA applications. Skills: • Excellent written and spoken English communication. • Strong project management, organizational, and result-oriented skills. • Ability to influence teams, work collaboratively in a matrix organization, and take ownership of deliverables. • Strong customer orientation, problem-solving, and strategic thinking. • Knowledge of EU & international regulatory requirements and frameworks. About the Organisation: A leading global pharmaceutical and life sciences company focused on innovative solutions for healthcare, life sciences, and electronics. The organization fosters a culture of curiosity, inclusion, and collaboration, emphasizing scientific excellence, regulatory compliance, and patient-centric innovation. Employees are encouraged to take ownership, innovate, and contribute to impactful global health outcomes.

Roles & Responsibilities: • Lead end-to-end dose surveillance activities across multiple clinical trials from start-up to close-out. • Perform routine and ad-hoc dose reviews, identify discrepancies, and coordinate follow-ups with sites and medical partners. • Document dose-related operational risks in SPOT/COSMOS, ensuring inspection-ready records. • Provide data-driven insights to trial teams, Clinical Monitoring Managers (CMMs), Medical Advisors, and functional stakeholders. • Ensure audit and inspection readiness, adhering to ICH-GCP, SOPs, and regulatory expectations. • Collaborate with Trial Managers on dosing and retention issues, strengthening relationships with site staff and internal partners. • Coach site staff to improve dose compliance and documentation quality. • Contribute to departmental training, knowledge sharing, and continuous improvement of surveillance methodologies. • Support global cross-functional improvement projects and drive innovation in dose surveillance processes. Qualification: • Graduate degree in Life Sciences (M-Pharma, PharmD, BDS/MDS, Pharmacy, MSc Nursing) with strong understanding of clinical trial conduct and ICH-GCP. Experience: • Minimum 4 years in clinical trials within pharmaceutical, biotech, CRO, or hospital settings. • Strong working knowledge of trial data, systems, and global clinical operations. • Experience collaborating with diverse global stakeholders. Skills: • Excellent communication, relationship-building, and stakeholder management skills. • Strong analytical mindset and familiarity with clinical IT systems. • Ability to independently solve complex issues in evolving environments. • High motivation, ownership, and continuous improvement mindset. • Ability to coach, influence, and guide site and internal staff effectively. About the Organisation: Novo Nordisk is a global biopharmaceutical company dedicated to defeating serious chronic diseases and improving long-term health outcomes. The Centralized Monitoring Unit (CMU) in Bangalore leads Risk-Based Quality Management (RBQM), ensuring robust oversight of clinical trial data, early risk identification, and mitigation strategies. The organization fosters innovation, collaboration, and excellence in clinical development, while maintaining a patient-centric, inclusive, and purpose-driven culture.

Roles & Responsibilities: • Perform medical review and clarification of trial-related adverse events (AEs) and post-marketing adverse drug reactions (ADRs), including narratives, coding, expectedness, seriousness, causality, and summaries. • Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases as per regulatory requirements. • Review coding of AEs, SAEs, SADRs, past medical history, concomitant medications, and other clinical data listings. • Serve as an internal consultant to pharmacovigilance case processing teams on assigned projects. • Perform medical safety review of protocols, Investigator Brochures, and Case Report Forms (CRFs) for safety content and data capture. • Provide aggregate reviews of safety information, including clinical data, post-marketing data, literature, and observational studies (e.g., DSUR, RMP, PBRER, ad hoc reports). • Lead and participate in training, product transitions, audit preparation, and knowledge exchange initiatives. • Review and approve Project Safety Plans and Medical Monitoring Plans per agreed medical safety scope. • Attend project and medical safety team meetings, representing safety and clinical data review findings to clients. • Act as Lead Safety Physician or provide backup support on assigned projects, including 24-hour medical support when required. • Support signal detection efforts and provide medical escalation support for regulatory and safety queries. Qualification: • Medical degree from an accredited and internationally recognized medical school. • Valid medical license or equivalent preferred. Experience: • Minimum 3 years of clinical practice experience post-medical degree. • Minimum 2 years of experience in the pharmaceutical industry preferred, or equivalent combination of clinical and pharma experience. • Knowledge of GCP, ICH guidelines, pharmacovigilance processes (ICSRs and aggregate reports), and departmental SOPs. Skills: • Strong medical knowledge and ability to evaluate safety data. • Experience with multiple safety databases and Microsoft Office (Word, Excel, PowerPoint). • Excellent verbal and written communication skills. • Ability to build and maintain effective working relationships with colleagues, clients, regulatory agencies, and study sites. About the Organisation: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company leverages data, technology, and advanced analytics to accelerate the development and commercialization of innovative medical treatments, improving patient outcomes and population health worldwide.