14 Clinical Evaluation Jobs

Company Overview Angel Care Hospital, a premier healthcare institution headquartered in Bangalore, is committed to delivering world-class healthcare services at an affordable cost. With a team of highly trained, qualified, and dedicated staff, the hospital provides patient-centered, high-quality tertiary and critical care. Serving the community with excellence, Spandana Hospital is a leading establishment in the Hospital Health Care industry. For more information, visit our website at https://spandanahospital.care . Job Overview Angel Care Hospital is seeking a dedicated and experienced Registered Nurse for our Outpatient Department (OPD). This is a full-time, mid-level position based in Ban...

Experience & Eligibility Criteria: 2-6 Years of experience with literature searches/ electronic literature databases and Clinical Evaluation Report (CERs) documents writing Education in any UG/PG in Life Science (1st Pref B/M Pharmacy). Job Description: Scientific Analyst (Scientific Literature search) Design of literature searches to be implemented in electronic literature databases Conducting systematic/targeted/structured literature reviews Developing and performing database searches and writing protocols and reports for literature reviews Identifying relevant evidence for research questions (Literature Screening) Summarizing literature review findings in a report Extracting, analyzing, a...

You will be responsible for ideating and participating in the development of evidence-based yet engaging content for various platforms including social media, ads, blogs, and ebooks. Your role will involve reviewing and evaluating content for accuracy, clinical relevance, and compliance with regulatory requirements. Collaborating with influencers and industry experts to create compelling content and build a strong network will be a key aspect of your work. Additionally, you will work closely with cross-functional teams, such as hardware, software, biotech, and marketing, to brainstorm new product features and support their launch. Ensuring that medical content aligns with product strategy, m...

The job involves counselling amputee clients on amputee rehabilitation exercise programs, limb management, pre and post-amputation counselling, explaining prosthetic services, gait training, and ADL training with prosthesis. The role also includes analyzing gait deviations and collaborating with clinical prosthetists to address issues, providing therapeutic management for gait-related problems, and identifying clients in need of wheelchair, seating, and mobility aid devices. A comprehensive clinical evaluation of clients requiring such aids is required, along with counseling patients and confirming cases related to prosthetics, wheelchairs, seating, and mobility aids. Additionally, the job i...

As a Consultant in Internal Medicine, you will be responsible for providing comprehensive care to adult patients with various medical conditions. Your role is crucial in accurately diagnosing conditions, creating effective treatment plans, and managing overall patient care to ensure high-quality healthcare and improved patient outcomes. Collaboration with other healthcare professionals, leading clinical practices, and continuous quality improvement are key aspects of this position. Keeping updated on the latest medical advancements, incorporating evidence-based practices, and maintaining the highest ethical standards are essential. This challenging yet rewarding role requires a combination o...

The healthcare team in Varanasi is looking for a dedicated and experienced Senior BAMS Physician to join them. As a Senior BAMS Physician, you will be responsible for providing expert Ayurvedic consultation and treatment to patients. Your role will involve diagnosing health issues, prescribing Ayurvedic therapies and medicines, maintaining patient records, and collaborating with other medical professionals for holistic care. Additionally, you will educate patients on Ayurvedic lifestyle practices and ensure high standards of hygiene, safety, and compliance within the clinic or hospital. To qualify for this position, you must have a Bachelor's degree in Ayurvedic Medicine and Surgery (BAMS) f...

As a Clinical Evaluation Medical Writer at Medtronic, you will play a crucial role in developing and updating clinical evaluation documents to support CE Mark submissions and ensure compliance throughout the product lifecycle. Your work will involve close collaboration with cross-functional teams to gather and interpret data on device safety, performance, and benefit-risk according to MEDDEV 2.7/1 Rev. 4 and EU Regulation 2017/745. You will also be responsible for summarizing and disseminating clinical literature and other available data to share relevant evidence, while managing Medical Information activities. This includes tracking inquiries, monitoring key metrics, researching and respond...

Job Purpose : (what contribution is this position supposed to make in business?) The QMS and EU MDR Compliance Executive is responsible for ensuring compliance with ISO 13485, EU MDR (Regulation EU 2017/745), and other applicable quality and regulatory requirements. This role will support the development, implementation, and maintenance of the Quality Management System (QMS), oversee documentation control, conduct internal audits, and support regulatory submissions and audits as required. Key Deliverables/Responsibilities of this position 1- Quality Management System (QMS): Maintain and improve the ISO 9001:2015 / ISO 13485:2016-compliant Quality Management System. Ensure effective implement...

You are a qualified and experienced medical professional sought to join the insurance operations team to handle and review Group Personal Accident (GPA) and Group Mediclaim (GMC) claims. Your responsibilities include ensuring the accuracy and appropriateness of claims, resolving medical disputes, addressing client grievances, and providing expert support in claim-related discussions with insurers and clients. Your key responsibilities will involve scrutinizing GPA and GMC claims from a medical perspective, handling disputed or complex claims such as accidental disability or death due to medical or accidental causes, and liaising with insurance company doctors and TPAs to resolve disputes bas...

Role & responsibilities Design effective product launch & training strategies to improve usage and adoption of UTD and Lexicomp, working clinical departments within hospital and academic institutions • Deliver engaging onsite and Live online (remote) training to end users to increase usage and awareness within each site • Ability to interface with customer contacts at all levels, to develop and strengthen relationships with multiple key contacts and influencers who can support, promote, and coordinate the promotion and use of our products • Uncover and address access challenges and resolve any technical barriers to usage • Provide consistent account feedback and market data to the sales, mar...

We are looking for a skilled and detail-oriented QA Executive to join our team. The candidate will be responsible for ensuring the quality and regulatory compliance of medical devices in line with EU MDR 2017/745 and Indian Medical Device Rules (IMDR). This role involves preparing, reviewing, and updating key technical and regulatory documentation and supporting post-market surveillance activities. Roles & Responsibilities Preparation, review, and updating of Technical Files as per EU MDR 2017/745 and Device Master Files (DMF) as per IMDR . Maintenance of General Safety and Performance Requirements (GSPR) documentation in compliance with applicable guidelines. Preparation of Risk Management ...

Experience & Eligibility Criteria: 2-6 Years of experience with literature searches/ electronic literature databases and Clinical Evaluation Report (CERs) documents writing Education in any UG/PG in Life Science (1st Pref B/M Pharmacy). Job Description: Scientific Analyst (Scientific Literature search) Design of literature searches to be implemented in electronic literature databases Conducting systematic/targeted/structured literature reviews Developing and performing database searches and writing protocols and reports for literature reviews Identifying relevant evidence for research questions (Literature Screening) Summarizing literature review findings in a report Extracting, analyzing, a...

Roles & Responsibilities Ensure on-time development and delivery of various sections of high-quality regulatory documents compliant with MEDDEV 2.7/1 Rev. 4. and MDR for Medical Devices across therapeutic areas Actively engage with internal stakeholders and cross-functional client business teams such as Medical Directors, Post Market Surveillance, Design Quality Engineers, R&D, and Regulatory Affairs Deliver solutions that are customized per client requirements in terms of language, content, format, and presentation Assist the Team Lead/Manager in the development of schedules to ensure timely delivery Manage timelines and communicate with team members to maintain awareness of expectations, m...

Experienced and licensed medical professional (MBBS/MD) with a strong background in medical claims assessment and clinical evaluation within the health insurance or TPA industry. Skilled in reviewing pre-authorization requests, hospitalization claims, and medical documentation to ensure medical necessity, policy compliance, and regulatory standards (IRDAI). Proficient in ICD-10 coding, claims adjudication, and fraud detection, with a focus on accuracy, ethical judgment, and collaborative decision-making. Adept at coordinating with hospitals, TPAs, and internal teams to streamline claim processing and maintain service quality.