Find Your Dream Medical Job in India

Role & responsibilities

Provide medical care to inpatients across various specialties Conduct daily ward rounds and monitor patient progress Manage medical emergencies and provide first-line treatment Assist consultants during procedures, surgeries, and clinical rounds Initiate investigations and prescribe medications as per protocols Coordinate referrals between departments when required

Handle emergency cases during duty hours and night shifts Ensure smooth clinical handover between shifts Respond promptly to code blue and emergency calls

Maintain accurate patient records, case sheets, and progress notes

Coordinate with nursing staff, ICU teams, diagnostic departments, and allied services Communicate effectively with patients and their families regarding treatment plans Participate in clinical meetings, audits, and quality improvement initiatives Adhere to infection control and patient safety protocols Report adverse events and participate in corrective actions Support continuous improvement in clinical care standards

Role: Medical Officer

Industry Type: Medical Services / Hospital

Department: Healthcare & Life Sciences

Employment Type: Full Time, Permanent

Role Category: Doctor

Education

UG: MBBS - Bachelor of Medicine and Bachelor of Surgery in Any Specialization

Key Responsibilities

• Support product lifecycle management through medico-marketing and medical strategy execution
• Review promotional materials and provide scientific inputs for launches and campaigns
• Plan and facilitate CMEs, advisory boards, symposiums, speaker programs, and scientific meetings
• Drive medical projects including registries, real-world evidence (RWE), and observational studies
• Build and maintain strong scientific relationships with KOLs and medical societies
• Develop scientific content, presentations, manuscripts, and support journal publications
• Support new product evaluation, competitor intelligence, and global scientific tracking
• Deliver therapy-area training and medical information to internal stakeholders
• Ensure compliance with internal policies and regulatory guidelines across all activities

Eligibility & Skills

Qualification: MBBS / MD / PhD / BDS / PharmD / M.Pharm / M.Sc

Experience: 0–3 years in Medical Affairs / Medical Services (Freshers can be considered only if MD; others must have relevant experience)

Key Skills & Requirements:

• Strong scientific communication and medical writing skills
• Ability to work with cross-functional teams and handle multiple projects
• Proactive, adaptable, and open to trav

Key Responsibilities:

•Lead Medical Affairs Strategy: Plan, prepare, and execute medical affairs strategies for key products within assigned therapeutic areas, ensuring alignment with overall business goals.

•Cross-Functional Collaboration: Collaborate with internal teams such as Marketing, Sales, Regulatory, and Clinical Research to drive product strategy, communication strategy, and interactions with external stakeholders.

•Medical Insights: Provide insights and feedback to the Clinical Research teams for new and ongoing clinical trials, development programs, and medical evaluations.

•Regulatory Input: Offer key medical input to Regulatory teams on product-related matters, ensuring alignment with medical and scientific goals.

•Research & Development Input: Offer key medical input on clinical relevance, guidelines and strength of evidence, strategic directions towards developmental methodology, changing global therapy landscape, public health perspectives of various R&D Projects.

•Clinical Research & Publication: Direct contribution to important CR Projects with critical medical input and drive publication of research work and other RWE projects.

•Medical Education: Lead and participate in various medical symposiums/events, including CME activities, “Key-Speaker-Training,” and expert meetings. Engage in medical education and digital education platforms for healthcare professionals (HCPs), driving physical-digital H

Continuia is a second-opinion platform for complex, high-stakes cases the ones where diagnosis is uncertain, the workup is incomplete, or the clinical picture doesn’t add up. We built it around a network of experienced physicians who review cases on their terms, not ours.

As a peer reviewer, you’ll receive curated cases not routine, not high-volume. You’ll produce structured second-opinion assessments asynchronously, on your schedule, with full clinical context provided. Diagnostic complexity is the norm here: multi-system presentations, ambiguous findings, cases where a second perspective genuinely moves the needle.

This is peer-level work. You’ll be part of a clinical network that takes rigor seriously, with structured tools that support your reasoning rather than shortcut it. If you’ve ever wished tumor boards and case conferences were easier to access this is built around that instinct.

What we’re looking for:

• MD or equivalent with an active license
• strong diagnostic reasoning, and the ability to write clear clinical assessments.
• Experience in diagnostics, internal medicine, or complex case management is a natural fit.
• Telemedicine or consultation experience is a plus.

Contract engagement. Remote. Flexible hours that fit around your existing practice.

Role: Senior Medical Safety Advisor

Total Experience: 5+ Years.

Pharmacovigilance/PV Experience : 1+ Years

Work location & Mode : PAN India -Homebased

Education : MBBS/MD Graduates.

Must Have Skills: Pharmacovigilance, ICSR.

Job Overview

The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of the product’s safety profile as well as other products within the same therapeutic area. Also, this position plays a greater role as a senior technical leader and participate in matrix management activities including preparation or participation in evaluating safety issues and preparation of aggregate reports in collaboration with the Post-Marketing Safety Experts and Safety Surveillance Group and be responsible for surveillance activities for selected products.

Essential Functions

• Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality, and company summary
• Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited ca

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 a

Company Description

HealthAssure Private Ltd. is a trusted name in the Primary health ecosystem, offering innovative solutions to enhance access to medical services.

The company has build a pan-India network across 1200 cities and over last 14 years of healthcare service providers, enabling better health outcomes and operational efficiency.

We have multiple lines of businesses from Insurance Medicals, Corporate Health Benefits and OPD Insurance and have serviced more than 13 million customers

Role Description

This is a full-time on-site role for the Business Head - Insurance Medicals, based in Mumbai.

The individual in this role will be responsible for

-engaging end to end our Insurance Relationships,

-Operational deliveries,

-building new sales and

-managing existing accounts

It would also include

• developing and implementing business strategies,
• fostering relationships with insurance and healthcare providers,
• analyzing industry trends to identify opportunities, and enable innovation
• ensuring the effective management of the division's financial and operational goals.
• team leadership, setting performance benchmarks, and ensuring client satisfaction.

Qualifications

• Strong experience and aptitude in Business Development, Strategic Planning, and Client Relationship M

Who we are

At Progenesis, we are a team of experts fighting against infertility issues that couples often face, ensuring

a hurdle-free journey towards pregnancy.

It was in 2014 when we first stepped into the area of healthcare with the sole motto of being companions

in highs & lows of couples journey to parenthood.

Company Website -

What you will do | Job Responsibility

● Proper and Detailed History Taking of the Patients.

● Counsel, the patient & the accompanying family members about the benefit of IVF and other

Line of Managements we Provide for Infertility Issues.

● Monitor the reporting & monitoring mechanism with respect to the quality at centre & the clinic

benchmark Adherence to SOP & Protocol.

● To check for various Consents in relevance to the Infertility Treatments we provide.

● Counselling Patients for Various services we provide to give Add on Results.

● To focus on patient Conversion.

● To guide the Smooth Functioning of OPD flow.

What you need to have | Job Specification

Experience 2 Years of Relevant Experience

Education B.A.M. S , B.H.M.S.

Language Marathi (Mandatory) Hindi and English

About Us : Kauvery Group of Hospitals launched its first hospital more than two decades ago. The founders of Kauvery Hospital were determined on creating world-class healthcare facilities that shall be affordable. The founding doctors set off on this dream in 1999 with a 30-bedded hospital in Trichy, focus on offering the best-in-class healthcare, with a personal touch. This was a very new concept in a tier 2 city like Trichy which lacked a tertiary care hospital at the time. Today, Kauvery is a multi-specialty hospital chain with 2250+ beds in six locations including Trichy, Chennai, Salem, Hosur, Tirunelveli and Bengaluru. With twelve hospitals and a workforce of over 8000+, Kauvery’s mission is to provide exemplary secondary and tertiary care

Our Vision

To be the most respected and trusted healthcare provider

Our Mission

To make great healthcare affordable

Our Values

• Continual Improvement
• Heartfelt Personal Touch
• Ethical
• Empathetic Care
• Real Accountability
• Service Excellence

Job Description

Position: Medical Administrator

Industry: Hospital / Healthcare

Role Overview

A Medical Administrator oversees the non-clinical operations of a hospital or healthcare facility, ensuring smooth functioning, regulatory compliance, and high-quality patient care support.

Hiring for an Reputed Insurance Company based at Muscat, Oman.

Job Title: Supervisor – Claims Audit & Risk (Medical Insurance)

Job Purpose

We are seeking a medically qualified professional to support Quality Assurance within the medical insurance function, focusing on claims auditing, utilization review, and risk identification with exposure to fraud detection . The role is ideal for candidates with strong clinical and insurance experience looking to expand into fraud and audit leadership.

Experience in utilization review, pre-authorization, medical claims auditing, and exposure to fraud detection and abuse patterns…

Key Responsibilities

• Perform detailed audits of inpatient and outpatient medical claims
• Identify irregularities, billing discrepancies, and potential abuse patterns
• Support investigations into suspicious claims and document findings
• Conduct retrospective reviews and assist in recovery of overpayments
• Apply clinical knowledge to evaluate treatment appropriateness and medical necessity
• Collaborate with providers and internal teams for claims validation and control measures
• Analyze claims data to identify trends and improvement opportunities
• Support development of reports and dashboards for audit tracking and savings
• Assist in provider reviews and highlight non-compliance or risk ind

About the Company

IKS Health enables the enhanced delivery of exceptional healthcare for today’s practicing clinicians, medical groups and health systems. Supporting healthcare providers through every function of the patient visit, IKS Health is a go-to resource for organizations looking to effectively scale, improve quality and achieve cost savings through integrated technology and forward-thinking solutions. Founded in 2007, we have grown a global workforce of 14,000 employees serving over 150,000 clinicians in many of the largest hospitals, health systems, and specialty groups in the United States.

IKS Health revitalizes the clinician-patient relationship while empowering healthcare organizations to thrive. We take on the chores of healthcare — spanning administrative, clinical, and operational burdens — so that clinicians can focus on their core purpose: delivering great care. Combining pragmatic technology and dedicated experts, our solutions enable stronger, financially sustainable enterprises. By bringing joy and purpose back to medicine, we’re creating transformative value in healthcare and empowering clinicians to build healthier communities.

Vision : Healthier Communities, Happier Clinicians, Thriving Organizations, Successful Healthcare for All.

Mission : Our mission is to enable the efficient delivery of excellent care. We will deliver on this promise in a man

Attention please！

• Only short NP-less than 30 days accepted, kindly pay attention to this to save your efforts, thank you for understanding

Project Description:

This role involves integrating bedside medical devices with healthcare systems to enable real-time clinical workflows and device-to-EHR data exchange. You will work with devices such as vital signs monitors, ventilators, infusion pumps, anesthesia machines, ECG/telemetry, and smart beds, ensuring seamless connectivity and compliance with healthcare standards. The position requires strong knowledge of HL7 messaging, device communication protocols, and troubleshooting connectivity issues. Exposure to FHIR/REST APIs and emerging technologies like AI (LLMs, Agentic AI) is a plus.

Responsibilities:

• Integrate bedside medical devices (vital signs monitors, ventilators, infusion pumps, anesthesia machines, ECG/telemetry, smart beds) with EHR systems.
• Implement and troubleshoot HL7 messaging (ADT, ORU, ORM) and flowsheet mappings.
• Support real-time clinical workflows and ensure accurate device-to-EHR data exchange.
• Configure and maintain serial-to-IP connectivity and converters for medical devices.
• Monitor device connectivity using SNMP, syslog, and other monitoring tools.
• Collaborate with clinical and IT teams to ensure compliance with healthcare standards.
• Document integration pr

Non-Clinical Job in US based MNC located in Vadodara, Gujarat Location (On-site job)

Company budget: 6,20,000 PA. (For FRESHER'S)

1-2 year experienced can get up to 8,50,000 PA.

About the Role - The role will be to review and verify large volumes of patient's full medical records with precision, perform clinical reviews as defined by the specific review methodologies and prepare a detailed report that includes chronologies and timelines, summaries, mass tort matrix and medical opinions on case validity and valuation.

Responsibilities

• Analyzing and summarizing medical records for pre and post settlement projects.
• Interpreting clinical data in terms of medical terminology and diagnosis.
• Adhering to company policies & principles, hence taking good care of Company culture.
• Adhere to Health Insurance Portability and Accountability Act (HIPPA) all the time.
• Daily reporting to Medical team lead for productivity & quality

Qualifications - MBBS (Freshers & Experienced both can apply)

BHMS & BAMS (2+ YEARS CLAIM PROCESS EXPERIENCE IN ANY INSURANCE SECTOR - Mandatory)

Required Skills

• Knowledge of basic level of health care data analysis and clinical review.
• Sound knowledge of medical terminology, ass

Company Description

Theia Health specialises in AI-powered automation of coronary CT scan analysis, aiming to accelerate and improve coronary artery disease detection, staging, and monitoring, particularly in the ASEAN region.

About the Role

We are seeking a Medical Imaging Annotation Specialist with a radiology background to support the development of AI models for medical imaging analysis. The role involves reviewing and annotating CT scan datasets, ensuring high-quality labelling of anatomical structures and pathological findings. This position plays a critical role in improving model accuracy and reliability by providing clinically accurate annotations and quality control for training datasets.

Key Responsibilities

• Review and analyse cardiac CT scan images to identify anatomical structures and relevant pathological findings.
• Perform precise medical image annotations according to internal annotation guidelines.
• Ensure high accuracy and consistency in labelling imaging datasets used for AI model training.
• Conduct quality checks and revisions of existing annotations to correct inaccuracies.
• Collaborate with the AI/ML team to refine annotation guidelines and improve dataset quality.
• Assist in identifying model errors by comparing AI predictions with ground truth annotations.
• Maintain proper documentation of a

Role Objective:

A key objective of this role is to lead and manage the end-to-end distribution and supply chain operations across the organization’s subsidiaries, ensuring efficient product availability, inventory management, logistics coordination, and distributor/channel performance across international markets.

The role oversees distribution operations across APAC, EMEA & LATAM regions, ensuring a 99% OTIF (On-Time In-Full) customer service level while continuously improving the end-to-end order-to-delivery experience.

The position is responsible for harmonizing supply chain practices across subsidiaries, optimizing logistics in terms of cost and delivery timelines, implementing regional warehouse strategies and ensuring product availability at branch locations through effective demand planning and coordination with sales, commercial teams, central planning and manufacturing plants. The role will also lead supply chain teams across subsidiaries as well as the corporate team responsible for servicing countries, ensuring alignment between demand, supply, inventory, and logistics operations.

Desired Candidate Profile:

• Education: Bachelor’s degree in Pharmacy / Science / Engineering / Supply Chain Management. MBA in Operations / Supply Chain is preferred.
• Experience: 15–20 years of experience in distribution, logistics, or supply chain management in pharmaceuticals / medical devices /

Job Title: Assistant / Associate Professor Medical Laboratory Technology (MLT) Location: MNR School of Medical & Health Sciences (MNR SMHS), Sangareddy

Job Summary: We are seeking a qualified and experienced professional in Medical Laboratory Technology (MLT) to join as Assistant/Associate Professor. The candidate will be responsible for academic teaching, laboratory training, and student mentoring, with a strong focus on diagnostic laboratory practices and quality standards.

Key Responsibilities:

• Deliver lectures and practical sessions in Medical Laboratory Technology
• Train and supervise students in clinical laboratory procedures
• Guide students during clinical postings in hospital laboratories
• Perform and demonstrate diagnostic tests in hematology, biochemistry, microbiology, and pathology
• Ensure proper usage and maintenance of laboratory equipment
• Maintain lab quality standards, safety, and infection control protocols
• Prepare lesson plans, assessments, and academic records
• Mentor students in academic and career development
• Participate in research, workshops, and institutional activities

Qualifications:

• Bachelor’s/Master’s degree in Medical Laboratory Technology (MLT) or related field
• 3–8 years of teaching and/or clinical laboratory experience

Key Skills:

• E

Overall Purpose of the Job

The Medical Writer is responsible for developing high-quality scientific and medical content for marketing, and clinical purposes. This includes creating submission-ready documents, ensuring compliance with medical, legal, and regulatory standards, and serving as the subject matter expert for scientific writing within the team.

Key Responsibilities

Content Development:

• Create accurate, clear, and compliant medical communications for various channels (e.g., Veeva-approved emails, CLMs, websites, videos).
• Draft and review promotional and educational materials for medical affairs.
• Review content/creative files developed from master assets and provide feedback based on client requirements

Regulatory & Compliance:

• Ensure adherence to Medical Legal Regulatory (MLR) approval processes.
• Manage referencing and annotation in Veeva Vault PromoMats.
• Perform reference and annotation of the promotional assets of Veeva Vault Promomat for further processing.

Scientific Expertise:

• Interpret and document clinical data accurately.
• Conduct literature searches and analyze client assets for evidence-based content.

Collaboration:

• Communicate effectively with cross-functional stakeholders to meet timelines.
• Provide intellectual input across multi

Esco Lifesciences Group provides enabling technologies, products, and services to the life sciences and healthcare industries, supporting academic research and scientific discoveries, clinical practice, as well as biopharmaceutical R&D and manufacturing. Headquartered in Singapore, Esco has an extensive sales network in over 100 countries, direct sales and service offices in over 20 countries, 8 manufacturing, and R&D hubs in the US, Europe, the UK, China, Singapore, Indonesia, and over 1300 employees worldwide.

Esco is poised to benefit from the sustained growth of the healthcare and biopharma industries in Asia and globally. Esco has achieved market leadership in China, and globally, in multiple categories within some of the fastest-growing segments — with China being its largest and fastest-growing market. As a Singapore-headquartered company, Esco is a nexus of East and West, bridging technologies, products, and talent across the world, with global operations spanning the US, Europe, and Asia.

Service Engineer for Medical

Responsibilities:

• Field service support for Esco products

• Handle all breakdown calls in the earliest response time

• Ensure high level of customer satisfaction and effectively manage customer expectations

• Prepares monthly reports to present the overall performance of the service and technical application management

• Monitors repairs and maintenanc

Job Description

1. Writing, editing, reviewing, formatting, publishing regulatory (clinical and post-marketing) documents and dossier sections in a manner compliant with FDA, EMA, CDSCO, ICH, CONSORT guidelines and other similar standards.

2. Collaborating with the clinical team in developing and strategizing the Clinical Development Plan. 3. Collaborating across line functions in preparing SOPs for Regulatory documents.

4. Interpreting, representing and summarizing clinical and scientific data.

5. Planning, organizing, tracking, and archiving clinical and post-marketing regulatory dossiers.

6. Managing stakeholders across line functions and geographies.

7. Managing assigned individual projects and holding complete responsibility throughout the document/project lifecycle.

8. Ensuring consistency at all times with compulsory and voluntary codes of conduct, appropriate legislations and compliance with internal SOPs.

9. Building-up newer competencies and enhance existing competencies; analyzing skill/process gaps and bridging the gaps by developing expertise/process maps. Developing cross-functional skills in publication writing.

10.

Training peers in regulatory writing.

11. Mentoring and coaching of direct reportees, if any

Position: Front Desk Receptionist

Experience: 2-5 Years

Qualification: Minimum bachelor’s degree / MBA will be an added advantage.

Location: Bund Garden Road, Pune, India

Type: Full-time — On-site (6 days/week)

Reports to: CX/Operations Lead / Clinic Head

Works with: Doctors, Nursing, Customer Service, Marketing, Accounts

Immediate Joinee Preferred

About Solo

Solo Clinic – IVF & ObGyn, a Center of Excellence in Obstetrics, Gynecology, Infertility & Laparoscopy. Founded in 1992, it offers ethical, data-driven, world-class fertility and laparoscopic care led by renowned expert Dr. Sunita Tandulwadkar.

Role Summary

This is one of Solo Clinic IVF’s most critical business roles. You are the first voice and first impression of the clinic and the person responsible for ensuring inquiries convert into consults, consults convert into therapies, and therapies convert into long-term relationships. You will own communication, coordination, tracking, follow-ups, and front-desk operations—nothing should slip.

Core Responsibilities

A) Communication & Patient Coordination (End-to-End)

1) First-time Inquiry Handling (Phone/WhatsApp/Walk-ins)

• Understand patient needs quickly; ask the right discovery questions.
• Explain Solo

We are seeking Psychiatrists (MD/DPM/DNB) to join our Offline Sexual Health Clinic in Madhya Pradesh. Our company is dedicated to improving the sexual health of individuals and communities through innovative technology and personalised medical care.

Locations in MP:

Indore

Gwalior

Jabalpur

Ujjain

Role:

-Part-time medical consultant for Allo Health's Offline Clinic (can be scaled to full-time)

-Timing: 3hrs fixed part time ( Between 4-9pm )

-Days: 6 days working with weekends mandatory (We get the highest demand). One day in the week between Monday and Friday will be your week off.

Eligibility:

-Psychiatrists (MD/DPM/DNB)

-Active medical license

-Fluent in English & Hindi

Process:

-15 days of orientation and training in the Sexual Medicine Certificate Course (done remotely)

-Start offline duty from the clinic.

A brief about Allo: We are India’s first dedicated Sexual Health Digital Clinic providing end-to-end solutions for all Sexual Health Disorders & Infections. We currently have 50+ clinics across Tier-1 and Tier-2 cities in India and are expanding further.

A few things you can go through to get a better understanding of us:

About us

-Website:

-Founder:

-Clinical Lead:

-Our Panel of HealthCare experts:

Company Description

Atean Healthcare Solutions is a specialized provider of cost-effective medical coding and medical billing services. The organization is committed to delivering accurate, efficient, and compliant solutions tailored to healthcare providers' needs. Atean Healthcare Solutions focuses on enabling healthcare organizations to optimize their revenue cycles while maintaining the highest standards of data integrity and compliance. With a client-centric approach, Atean is a trusted partner for healthcare businesses aiming to streamline operations.

Role Description

This is a full-time, on-site role for a Medical Billing Coder located in Chennai. Responsibilities include accurately coding medical records, analyzing and assigning proper healthcare codes for diagnoses and procedures, and ensuring compliance with relevant coding guidelines and regulations. The role involves reviewing patient data for completeness and accuracy, collaborating with healthcare providers for clarification, and staying updated on ever-evolving coding standards and facilitating timely claim submission and reimbursement.

Roles and Responsibilities:

• Review patient medical records, physician notes, and clinical documentation to determine appropriate codes
• Assign accurate ICD-10, CPT, and HCPCS codes for diagnoses and procedures
• Ensure coding accuracy and compliance with healthcare regulations and

About Alkem:

Alkem Laboratories Limited is an Indian multinational pharmaceutical company headquartered in Mumbai, that manufactures and sells pharmaceutical generics, formulations and nutraceuticals in India and globally over 50 countries. We have consistently been ranked amongst the top five pharmaceutical companies in India. Our portfolio includes illustrious brands like Clavam, Pan, Pan-D, and Taxim-O, which feature amongst the top 50 pharmaceutical brands in India.

Objective / Purpose of the Job:

To actively contribute to the organization/division by taking responsibility for the scientific, technical, and ethical soundness of all policies, statements, and endeavors.

To support the division medically in all activities related to the portfolio and provide high-quality and timely service to internal and external stakeholders.

Key Result Areas / Accountabilities:

• To actively support the development of promotion of allocated portfolio under supervision from the Line manager or the mentor, provide strategic inputs and support towards the creation of marketing/brand plans/medical development plans, and towards design and execution of medical-marketing programs/clinical programs, including initiatives to enhance access to medicines
• Under supervision from the Line manager or mentor, create/review promotional, training, and Continuing Medical Education (CME) mate