25 Medical Support Jobs

- Assist patients in multiple hospitals at the given location with insurance form filling for the prescribed therapy, collect/verify documents, resolve discrepancies, and ensure compliance. - Maintain accurate records, update CRM, track form status. Required Candidate profile - Any graduate capable of health insurance / data entry / form processing is an advantage. - Good communication skills in English & Local Language - Proficiency in basic computer applications.

As a General Manager reporting to the Sr. VP of Clinical Research, you will be responsible for overseeing various aspects of clinical trials and BA-BE studies. With an educational background of MBBS and MD, you are expected to bring 15-20 years of experience to the role. Your primary duties will include preparing, reviewing, and approving clinical trial documents, providing medical support to the study team, and assisting in regulatory approvals in NDAC Meetings. Your role will also involve CRO evaluation and selection for outsourcing clinical research projects, as well as preparing and implementing CAPA. Real-time management of SAEs and monitoring responsibilities will be crucial aspects of your job. Additionally, you will be involved in developing clinical trial documents, assisting in site feasibility and selection, and conducting site initiation, interim monitoring, and close-out visits. In the realm of medical writing, you will be responsible for preparing medico-regulatory documentation, SmPC, package inserts, patient information leaflets, clinical overviews, summaries, expert reports, safety efficacy reports, and more. Your technical skills should include a solid understanding of medical concepts, clinical trial designs for vaccines, pharmacokinetics, and safety evaluation. Being a team player with attention to detail, good analytical skills, and effective communication abilities will be essential for success in this role. Overall, your role as a General Manager in Clinical Research will require a project-oriented approach, strong scientific acumen, and the ability to collaborate effectively with various stakeholders to ensure the successful execution of clinical trials and research projects.,

IntegriMedical is a market leader in providing comfort for patients and transformative safety for healthcare professionals through Needle Free Drug Delivery Technology. Our global teams design, develop, manufacture, and sell Needle Free Injection Systems (NFIS) worldwide. Using high velocity mechanical power, our NFIS effectively and consistently administer biologics and drugs. Approved for use in multiple markets, our innovative solutions allow healthcare providers to focus fundamentally on patient care. We are seeking a dynamic and proactive "Application Specialist" to join our team in Bangalore. In this role, you will work closely with nursing staff and healthcare professionals, manage vaccination processes, monitor training sessions, and foster strong relationships with children's parents and the healthcare team. This position offers an excellent opportunity for someone looking to grow in the healthcare industry, from entry-level to advanced experience. The ideal candidate will have experience or interest in healthcare, nursing, or medical support roles. Strong communication and interpersonal skills are essential, with the ability to build rapport with both nursing staff and parents. The ability to work in a fast-paced environment and manage multiple tasks effectively is crucial. Excellent presentation skills are also required to represent the organization professionally.,

Are you an experienced medical professional passionate about Medical Affairs Do you thrive in a dynamic environment and enjoy implementing medical affairs strategies Novo Nordisk India Private Limited is looking for a Regional Medical Advisor to join their Semaglutide North department. In this role, you will actively contribute to medico-marketing activities and support the implementation of the Medical Affairs strategy in the country. Your responsibilities will include: - Executing the Indian medical strategy in your designated region. - Building and maintaining strong scientific relationships with key influencers and stakeholders. - Conducting training and educational activities for Physicians and other Health Care Professionals (HCPs) specializing in diabetes and obesity. - Providing medical support to the brand team. - Assisting the marketing and sales team in developing product and promotional strategies, anticipating market challenges, and taking timely actions. - Keeping updated on scientific knowledge through participation in scientific meetings, gathering insights from key opinion leaders, and communicating with internal stakeholders. - Educating and training field and marketing personnel on disease, product, and therapy aspects relevant to the promotional strategy. - Establishing a strong advocacy of Novo Nordisk's portfolio with key external stakeholders through ongoing scientific interactions. To qualify for this position, you should hold an MBBS/MD in Pharmacology from a reputed institution. Strong scientific knowledge and interest in diabetes and obesity, collaboration skills, communication abilities, and analytical capabilities are essential. Additionally, skills in planning, execution, and follow-up, along with a creative and innovative attitude, are required to excel in this role. The Clinical, Medical, and Regulatory (CMR) department at Novo Nordisk is known for its diversity and collaboration. From interactions with healthcare professionals to regulatory strategies and medical education, CMR plays a crucial role in supporting Novo Nordisk's products with a patient-centered focus. At Novo Nordisk, every day is dedicated to finding solutions for defeating serious chronic diseases. The company values an unconventional spirit, determination, and curiosity in approaching work. With a focus on improving patients" quality of life through innovative solutions, Novo Nordisk is committed to making a difference in healthcare. If you are ready to contribute to Novo Nordisk's mission, apply by submitting your CV and motivational letter online before the deadline on 12/08/2025. Internal candidates are advised to inform their line Managers before applying. Novo Nordisk emphasizes an inclusive recruitment process and equal opportunities for all job applicants. The company does not extend unsolicited employment offers or charge fees to prospective employees during the recruitment process. Join Novo Nordisk in shaping the future of healthcare with an unordinary approach that drives real, lasting change in health.,

Job Description: As a Drug Safety Physician at ICON, you will play a crucial role in providing medical and safety support to the activities of ICON Project Teams. Your primary responsibility will be to ensure that projects are conducted in adherence to the highest ethical principles and medical standards, following Good Clinical Practice (GCP) and good pharmacovigilance practices, and in compliance with applicable legal and regulatory standards. Your key responsibilities will include reviewing and accurately assessing Adverse Events (AEs) and Adverse Drug Reactions (ADRs) in terms of seriousness, expectedness, listedness, and relatedness using coding such as MedDRA. You will also be responsible for reviewing aggregated reports, providing safety profile assessments, identifying safety issues in clinical trials or post-marketing settings, and escalating them to the appropriate channels within ICON for resolution with the client. Additionally, you will be involved in providing support and training on regulatory requirements for expedited and periodic reporting of AEs/ADRs, participating in project-related meetings, communicating with the client as per the Project Specific Procedures, assisting in code-break activities, reviewing and providing input to product information, and offering pharmacovigilance consultancy to clients regarding regulatory reporting requirements. Furthermore, you will provide guidance to Medical and Safety Services staff on regulatory reporting of adverse events and undertake any other responsibilities as assigned. Your role will require collaboration, communication, and a commitment to upholding the highest standards of patient safety and regulatory compliance. Role requirements: To be successful in this role, you should be a qualified and licensed physician with 2-3 years of patient diagnosis and treatment experience in a hospital-based setup. Prior experience in clinical research or pharmacovigilance is optional but beneficial for this position. Benefits of Working in ICON: At ICON, we value our people and strive to create a culture that rewards high performance and fosters talent development. We offer competitive salary packages that are regularly benchmarked against industry standards, with annual bonuses tied to performance goals for both the organization and individuals. In addition to competitive salaries, we provide a range of health-related benefits for employees and their families, as well as comprehensive retirement plans and life assurance to support long-term financial planning. Our work environment encourages individuals to pursue their sense of purpose and drive meaningful change, contributing to a fulfilling career at ICON. What ICON can offer you: In addition to competitive compensation, ICON provides a variety of benefits tailored to support employee well-being and work-life balance. These benefits include various annual leave entitlements, diverse health insurance options, retirement planning offerings, and a Global Employee Assistance Programme for 24-hour access to specialized professionals for support. We also offer life assurance and country-specific optional benefits such as childcare vouchers, bike purchase schemes, discounted gym memberships, and health assessments to promote employee well-being. At ICON, we are committed to diversity, inclusion, and supporting our employees in achieving their personal and professional goals. If you require a reasonable accommodation for any part of the application process due to a medical condition or disability, please inform us so we can assist you accordingly. Interested in joining ICON but unsure if you meet all the requirements We encourage you to apply regardless, as your unique skills and experiences may align with our needs for this role or other opportunities within the organization. At ICON, we are always looking for talented individuals who share our vision and values.,

As a Medical Advisor at our company, you will be responsible for supporting medical and scientific initiatives related to our product portfolio. Working closely with internal teams including regulatory, marketing, and R&D, you will ensure that our products are supported by accurate clinical data and adhere to industry regulations. Your role will be crucial in generating medical insights, supporting product launches, providing medical information, and ensuring the safe and effective use of our products. You should hold a degree in MBBS, BDS, PharmD, or a related field, with a preference for a Masters Degree or relevant certifications in Medical Affairs. Ideally, you will have 2-3 years of experience in medical affairs, clinical research, or a similar role within the pharmaceutical industry. Exposure to scientific communications, clinical data interpretation, or medical support in product launches will be advantageous. Your responsibilities will include supporting the development and dissemination of clinical and scientific data to ensure product safety and effectiveness, providing medical expertise during product launches and marketing activities, and collaborating with internal teams to align medical and scientific information. Additionally, you will assist in preparing scientific reports, presentations, and medical education materials, ensuring compliance with regulations and internal policies, and participating in medical training sessions for internal teams. Key performance indicators for your role will include the accuracy and timeliness of clinical and medical data dissemination, contribution to product launches and alignment with marketing strategies, compliance with industry regulations and company policies, and participation in internal medical training programs. To succeed in this role, you should possess a strong understanding of clinical data and medical communications, excellent communication and presentation skills, the ability to collaborate with cross-functional teams, strong attention to detail and organizational skills, knowledge of pharmaceutical regulations and industry standards, and proficiency in medical writing and scientific documentation. Your operating network will include internal stakeholders such as the Head of Medical Affairs, Regulatory team, Marketing team, R&D, and Sales team, as well as external contacts in healthcare professionals and scientific communities.,

The position within the EPD Medical organization with medical/scientific qualifications involves providing scientific/medical support in a non-sales capacity. This role requires significant contact with Abbott customers in the field while excluding employees primarily involved in monitoring or managing clinical studies. Reporting to the Senior Manager RMA/Head RMA, the role entails participation in the initiation, oversight, and follow-up of clinical studies and medical projects within the EPD Medical Organization. Activities must adhere to relevant processes and procedures, with collaboration among key members of the EPD Medical Organization, such as Medical Managers, Clinical Research Managers, and Medical Advisors, in the respective therapeutic area. The role includes fostering relationships, enhancing the Company's scientific credibility with Regional/National Opinion leaders, providing scientific and medical information, and maintaining key scientific knowledge for effective communication with physicians and opinion leaders. Responsibilities: - Ensure compliance with local, global, and national laws, regulations, guidelines, codes of conduct, and Company policies - Offer scientific and technical support to key opinion leaders and academic centers, facilitating access to current medical and scientific information - Design and deliver engaging high-science activities for Physicians and Key Opinion Leaders to drive Therapy Shaping - Assist in the oversight of clinical studies and medical projects within the relevant therapeutic area - Deliver unbiased scientific presentations to physicians individually or in groups - Collaborate in selecting qualified physicians for research collaborations or lecture/meeting support - Stay updated on competitor intelligence and communicate relevant information within the Company - Support Medical/Marketing teams in gathering insights from HCPs and Patients for brand plans/New products - Attend Scientific Societies meetings and Conferences, providing summaries of key messages for internal use - Assist physicians in directing requests for access to Company products based on legal and regulatory requirements - Support sales/marketing/internal teams in enhancing scientific and technical expertise - Participate in real-world data collection programs alongside Medical Affairs & Clinical Operations team Technical Competencies: - Therapeutic Area Expertise - Management Skills - Communication Skills - Compliance & Process Improvement Skills - Problem/Conflict Solving Ability - Priority Setting - Relationship Building Core Competencies/Attributes: - Adaptability - Initiative - Innovation - Integrity - Teamwork & Collaboration Key Interfaces: - EPD medical personnel, Marketing department, Sales organization, Healthcare personnel, Patients, Research Investigators, Key Opinion leaders, Institutions, Scientific or Medical Societies, International Medical Development/Global Project Team personnel Reporting Lines: - This position reports to the medical department's Senior Manager RMA/Head RMA Location: - Field-based Ideal Candidate Criteria: - Graduate or Post Graduate Medical Degree in Pharmacology or Allied Sciences - Keen interest in developing and maintaining expert knowledge in the assigned therapeutic area/product and medical research - Knowledge of scientific methods in clinical research and legislative/regulatory controls - Strong commitment to compliance, scientific quality, and integrity - Proficient in spoken and written English Career Development: Possible career development roles include Manager-Medical Affairs or Medical Advisor, Head of Affiliate Medical, Area Medical Advisor, EPD Strategic Medical Affairs, Clinical Development, GPRD, I & D, and Product Management.,

Job Title: Staff Nurse Location: Thoothukudi Department: Nursing/Healthcare Reports To: Nurse Supervisor/Head Nurse Job Summary: The Staff Nurse will provide high-quality patient care in accordance with clinical protocols, policies, and ethical standards. This role includes assessing patient needs, delivering medical care, and supporting recovery while maintaining a compassionate and professional approach. Key Responsibilities: Patient Care: Assess, plan, implement, and evaluate individualized care for patients. Monitor and record patient vital signs, symptoms, and medical history. Administer medications, injections, and treatments as prescribed by physicians. Medical Support: Assist doctors during examinations, procedures, and surgeries. Prepare and maintain equipment for diagnostic and therapeutic procedures. Provide wound care, dressing changes, and other nursing interventions. Documentation and Reporting: Maintain accurate and detailed patient records. Report any changes in patient condition to the medical team promptly. Ensure compliance with documentation standards and confidentiality protocols. Health Education and Counseling: Educate patients and their families about health conditions, treatments, and preventive care. Provide emotional support and guidance to patients and families during recovery. Team Collaboration: Work closely with other healthcare professionals to develop and implement patient care plans. Participate in interdisciplinary team meetings and case discussions. Supervise and guide junior nursing staff and trainees when required. Safety and Hygiene Compliance: Adhere to infection control policies and procedures. Ensure proper sterilization of equipment and cleanliness of the healthcare environment. Respond effectively to medical emergencies and follow safety protocols. Qualifications and Skills: Educational Requirements: Diploma/Bachelors Degree in Nursing (B.Sc Nursing or DGNM). Licensure: Registered Nurse with a valid [Insert country/state] Nursing Council license. Experience: 13 years of nursing experience (freshers may also apply depending on role specifics). Skills: Proficiency in patient assessment and clinical care. Knowledge of medical terminology and procedures. Excellent communication and interpersonal skills. Empathy, patience, and ability to handle stress in challenging situations. Key Competencies: Attention to detail and critical thinking. Strong organizational and time management skills. Ability to work collaboratively in a team-oriented environment. Commitment to patient safety and quality care. Work Environment: May require standing for extended periods and working in shifts, including nights, weekends, and holidays. Exposure to potentially infectious materials and stressful situations.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.

Act as a bridge between pharma companies and healthcare professionals, providing medical insights and scientific support.