5 Medical Review jobs in India

Assoc Medical Data review Manager

Bengaluru, Karnataka IQVIA

Posted 5 days ago

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Job Description

Job Title / Primary Skill: Associate Medical Data Review Manager

Years of Experience: 2 + Years.

Job Location: Bangalore/Thane (Hybrid)

Educational qualification: MBBS/MD is a must.


Job Overview:

  • Serve as a Subject level Data reviewer (SLDR) and identify any anomalies in patient reported data by performing Subject
  • Level Data Review that requires further investigation with the clinical site to determine overall accuracy
  • Conduct in-stream data trend analysis in support of data quality and integrity (includes protocol compliance and targeted review of patient data)
  • Provide project management to the team in the area of Project Management and viewed as an expert in data management.
  • Drive the delivery of end-to-end study data quality and integrity.
  • Provide medical, clinical, and scientific advisory expertise.
  • May act as a clinical data scientist for performing data analytics by reviewing the visualizations, identify potential issues of concern and present at multi-disciplinary team meetings and external meetings.
  • Ensure data quality focus to audit readiness with Clinical Compliance and Systems Validation Compliance. .
  • Define data capture requirements in line with protocol and reporting needs.
  • Maintain strong customer relationships
  • Ensure timely follow-up and resolution of compliance issues
  • Serve as Subject Matter Expert (SME)
  • Serve as POC/ Back-up POC


REQUIRED KNOWLEDGE, SKILLS AND ABILITIES


  • Good understanding of clinical/medical data.
  • Knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology.
  • Proven expertise in the proactive identification of issues.
  • Demonstrated ability to plan, organize and manage resources to bring to successful completion specific study or project goals and objectives in accordance with defined quality and time based metrics.
  • Proven ability to work within a matrix team environment requiring minimum level of supervision


MINIMUM REQUIRED EDUCATION AND EXPERIENCE

  • MBBS or MD with 2 + years of work experience.
  • Experience in clinical data sciences at a CRO, pharmaceutical company or other medical environment with demonstrated leadership experience
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Medical Records Technician

Dr. Moopens Medical College

Posted 23 days ago

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Job Description

full-time

Company Overview

Dr. Moopens Medical College is a prominent institution in the Hospital & Health Care industry, located in Meppadi, Wayanad, Kerala. With a workforce of employees, the college is dedicated to providing exceptional medical education and healthcare services. For more details, visit our website at


Job Overview

We are seeking a Medical Records Technician to join our team at Dr. Moopens Medical College in Wayanad. This is a full-time position suitable for candidates with 1 to 2 years of experience. The ideal candidate will have proficiency in handling electronic health records and managing health information efficiently.


Qualifications and Skills

  • Diploma/Degree/Masters in Medical records.
  • Proficiency in electronic health records systems for efficient medical data management (Mandatory skill).
  • Accurate data entry skills to ensure precise recording and updating of patient information (Mandatory skill).
  • Understanding of health information management principles to maintain and organize health records effectively (Mandatory skill).
  • Knowledge and application of ICD-10 coding standards to ensure accurate diagnosis and billing processes.
  • Experience with medical billing software for processing and tracking healthcare billing operations.
  • Familiarity with HIPAA compliance standards to guarantee patient information privacy and security.
  • Good command of Microsoft Office Suite to support various administrative tasks and report generation.
  • Attention to quality assurance for ensuring accuracy and consistency of medical records and documentation.


Roles and Responsibilities

  • Manage and maintain accurate and up-to-date electronic health records for all patients.
  • Input, process, and verify the integrity of patient data into EHR systems effectively.
  • Collaborate with medical staff to ensure accurate and complete documentation of patient information.
  • Adhere to HIPAA guidelines to maintain confidentiality and organization of patient health information.
  • Assist in the coding and classification of diseases, procedures, and other medical information according to ICD-10 standards.
  • Analyze and review medical records for accuracy, completeness, and quality assurance purposes.
  • Support billing operations by ensuring correct and timely submission of claims and insurance requirements.
  • Participate in ongoing training and development to stay current with EHR systems and healthcare industry standards.
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Medical Records Technician

Chikkaballapur, Karnataka Refining Skills Academy

Posted 23 days ago

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Job Description

full-time
Medical Records Technician


Location: Muddenahalli, Chikkaballapur, Karnataka

Experience: Minimum 2 years in hospital medical records or health information management

Qualification: Diploma or Degree in Medical Records Technology / Health Information Management

Employment Type: Full-time | 6-day workweek


Why Join Us?

At SMSIMSR , accurate and timely medical documentation is at the heart of effective and ethical patient care . As a Medical Records Technician , youll play a key role in organizing and maintaining patient records , supporting clinical departments, and ensuring compliance with regulatory and data protection standards .


This is an excellent opportunity for someone with attention to detail and familiarity with hospital systems , looking to contribute to a healthcare institution focused on service, learning, and transparency .


Key Responsibilities:

Maintain and update electronic and physical medical records of inpatients and outpatients

Ensure accuracy, completeness, and timely entry of patient information into the hospital database

Support clinical departments, insurance teams, and administrative units in retrieving patient records

Ensure strict confidentiality and compliance with data privacy protocols and hospital policies

Work with doctors and nurses to clarify case details, discharge summaries, and missing documentation

Organize medical record files, reports, X-ray films, and lab reports in structured formats

Assist in internal audits, data requests, and statutory inspections

Maintain records in compliance with NMC, NABH, and health authority guidelines


What We Offer:

Structured, process-driven work environment

Exposure to hospital health information systems (HIS)

Opportunities for skill development in hospital informatics and compliance

Housing and other benefits discussed during hiring


If you are an organized and detail-oriented professional passionate about supporting healthcare operations, apply now!

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Medical Reviewer MLR, Scientific Communications

Hyderabad, Andhra Pradesh Amgen

Posted 2 days ago

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Job Description

**Role Description:**
The Scientific Communications MLR Technical Reviewer is responsible for checking all medical content for data and scientific accuracy, and reference appropriateness for materials submitted through the Medical, Legal, and Regulatory (MLR) process. This role ensures that all content adheres to Amgen's scientific and compliance standards, while supporting timely review and approval of assets that inform and engage healthcare providers, patients, and internal stakeholders.
Working closely with the US Scientific Communications MLR Reviewer, the Technical Reviewer brings scientific expertise, attention to detail, and compliance awareness to evaluate the submissions. This role contributes to the quality and consistency of Amgen's communications by safeguarding scientific integrity across materials.
**Roles & Responsibilities:**
+ Conducting a review of proactive materials for scientific accuracy and reference appropriateness
+ Reviewing the material and ensuring appropriate medical context, scientific balance, and compliance are maintained in submitted content
+ Ensuring the timely and high-quality review of MLR materials within established SLAs and agreed-upon timeframes
+ Collaborating with the US Scientific Communication MLR Reviewer to ensure clear guidance on action items
+ Working within Amgen's MLR systems to apply clear review comments per company process
+ Conducting and participating in knowledge-sharing sessions to align on therapeutic areas, products, and review best practices
+ Providing scientific guidance to cross-functional teams regarding appropriate interpretation and use of data in promotional and medical content
+ Supporting standardization of review practices, templates, and criteria to drive efficiency and consistency across reviews
+ Staying current on therapeutic area developments, industry guidelines, and regulatory requirements relevant to MLR reviews
+ Contributing to process improvement initiatives and adoption of new technologies that enhance review workflows
**Basic Qualifications and Experience:**
Doctorate degree & 2 years of directly related experience
OR
MBBS or Master's degree & 4 years of directly related industry experience
OR
Bachelor's degree & 4 years of directly related industry experience
OR
Associate's degree & 6 years of directly related industry experience
**Functional Skills:**
**Preferred Qualifications:**
+ Doctorate degree in life sciences, pharmacy, biomedical sciences, or a related field
+ 5+ years of experience in medical review, medical writing, scientific communications, publications, or related industry role
+ Familiarity with the MLR review process and regulatory requirements for medical and promotional materials
+ Strong ability to critically evaluate data, references, and claims for scientific accuracy and compliance
+ Prior experience with content management and MLR review systems (e.g., Veeva PromoMats or equivalent)
+ Excellent attention to detail and organizational skills to manage multiple, concurrent submissions under tight timelines
+ Strong written and verbal communication skills to interact effectively with cross-functional stakeholders
+ Knowledge of therapeutic areas such as oncology, cardiovascular, inflammation, bone, and rare diseases is a plus
+ Understanding of US compliance, copyright, and transfer-of-value requirements
**Competencies:**
+ **Scientific Integrity:** Upholds rigorous standards in data accuracy and interpretation
+ **Collaboration:** Works effectively with cross-functional global teams in MLR review cycles
+ **Attention to Detail:** Ensures consistency, accuracy, and compliance in content review
+ **Time Management:** Prioritizes high-volume review workload and meets critical deadlines
+ **Adaptability:** Adjusts to evolving review practices, systems, and regulatory expectations
+ **Compliance:** Demonstrates commitment to integrity in all aspects of review work
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
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Medical Reviewer-Drug Safety Physician

Bengaluru, Karnataka Indegene

Posted 5 days ago

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Job Description

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out Looking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast track career where you can grow along with Indegene’s high-speed growth. We are purpose-driven. We enable healthcare organizations be future ready and our customer obsession is our driving force. We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work. If this excites you, then apply below:


Job Title: Medical Reviewer – Pharmacovigilance

Location:

Work from office: Bangalore, Hyderabad, Mumbai, Pune, Delhi

Willingness to relocate to one of the above locations is mandatory.

Education Requirements:

  • MBBS and MD (mandatory)
  • Candidates without both qualifications will not be considered.


Job Title: Medical Reviewer – Pharmacovigilance

Location:

Work from office: Bangalore, Hyderabad, Mumbai, Pune, Delhi

Willingness to relocate to one of the above locations is mandatory.


Education Requirements:

  • MBBS, MD(mandatory)
  • Medical council of India registration ( Mandatory)



Job Description:

As a Medical Reviewer – Pharmacovigilance , you will be responsible for the comprehensive medical review of individual case safety reports (ICSRs) and ensuring compliance with regulatory and client-specific requirements. You will play a critical role in safeguarding patient safety through high-quality medical evaluation and regulatory reporting.

Key Responsibilities:

  • Perform medical review of ICSRs for accuracy , medical relevance , and consistency with the source documents and safety database entries, in alignment with client requirements.
  • Conduct second-level triaging of non-serious cases to identify any potential serious adverse events (SAEs), as per client-specific conventions.
  • Review and validate:
  • Suspect product coding
  • Event selection and MedDRA coding (current version)
  • Grouping/subsuming and event ordering
  • Confirm and correct:
  • Event coding and classification
  • Ranking of events, seriousness criteria, and listedness/expectedness
  • Perform comprehensive medical evaluation of adverse event reports including serious/expedited cases and pregnancy-related reports.
  • Assess adverse events for seriousness , listedness , and causality , ensuring all medically relevant data from source documents is accurately reflected.
  • Review and enhance narratives in compliance with client conventions.
  • Provide or verify company pharmacovigilance (PV) comments as needed.
  • Initiate appropriate follow-up queries based on the clinical context of the case.
  • Identify and escalate potential safety signals or concerns in line with client procedures.
  • Ensure completeness and medical soundness of cases before providing final medical sign-off .
  • Assess malfunctions and serious injury/death outcomes in relation to combination products.
  • Participate in literature surveillance and aggregate report medical review, ensuring compliance with regulatory timelines and SOPs.
  • Track and document inconsistencies in data entry and provide feedback for continuous improvement.
  • Collaborate closely with cross-functional teams to maintain scientific accuracy , clarity , and regulatory compliance in all case documentation.
  • Stay updated with international pharmacovigilance regulations and follow all applicable SOPs , guidelines , and best practices .
  • Attend mandatory internal and client-specific trainings to ensure continuous compliance.

Required Skills and Competencies:

  • Strong analytical and critical thinking abilities
  • High attention to detail and scientific accuracy
  • Sound medical judgment and decision-making in line with pharmacovigilance standards
  • Proficiency in medical terminology , disease pathology, pharmacology, and therapeutics
  • Ability to analyze and interpret adverse event data
  • Strong written and verbal communication skills
  • Good comprehension and the ability to summarize complex medical data
  • Team player with effective interpersonal and collaboration skills
  • Familiarity with pharmaceutical industry practices and drug development processes (preferred)


Additional Requirements:

  • Willing to relocate to any of the listed office locations.
  • Ready to work from the office with hybrid options
  • Must possess MBBS and MD degrees (non-negotiable)



EQUAL OPPORTUNITY:

Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

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