29 Healthcare jobs in Aurangabad

Job Description – Healthcare Data Engineer – AI/ML Enablement

Location: Remote

Type: Contract

Accelyst is an innovative AI Consultancy that leverages a unique catalog of industry specific Agents and leading-edge AI platforms to deliver tangible, integrated, secure and ROI-optimized solutions. We combine deep industry and technical expertise to enable rapid deployment of innovative AI-driven capabilities to augment and automate client workflows for employees, customers, prospects, and investors.

Why Accelyst?

Join Accelyst to be part of a dynamic team that leverages AI-driven technology to make a positive impact. Our leadership, with Big Four Consulting experience, fosters a nimble, client-focused environment, minimizing bureaucracy to enhance delivery and professional growth. You'll work on complex AI projects that challenge and inspire, meeting high client expectations. Additionally, we benefit from our profit-sharing model, reflecting our commitment to respect and integrity for all employees.

Role Overview

We are seeking a Healthcare Data Engineer to support AI/ML initiatives through advanced data preparation and management. This role involves cleaning, rationalizing, normalizing, and integrating large healthcare datasets (claims, member, provider, clinical data) to ensure readiness for AI-driven analytics and automation. You will collaborate with data scientists, engineers, and AI teams to deliver high-quality, compliant data pipelines for predictive analytics, risk stratification, fraud detection, and other use cases.

In this role, you will be responsible for designing, developing, testing, and integrating data solutions to support automated workflows, bots and AI Agents that span legacy platforms, such as:

• Claims processing systems
• Member management platforms
• Provider network management systems
• Care management platforms

Responsibilities

• Perform data cleaning : identify and resolve errors, inconsistencies, duplicates, and missing values.
• Conduct data rationalization and normalization to align with healthcare data standards and structures (ICD-10, CPT, SNOMED).
• Aggregate and consolidate datasets from multiple systems (EHRs, claims, third-party vendors).
• Execute data extraction workflows to generate AI-ready features.
• Conduct data quality assurance and validation checks to ensure reliability and accuracy.
• Collaborate with data scientists and AI/ML teams to align data preparation with project goals.
• Implement automation and scripting for efficient data handling.
• Maintain thorough documentation of data processes, transformations, and metadata.
• Ensure compliance with HIPAA, data governance, and security standards .

Qualifications

• Strong experience in healthcare data engineering (claims, EHR, clinical datasets).
• Proficiency in data cleaning, normalization, aggregation, and feature extraction .
• Knowledge of healthcare standards and coding systems (ICD-10, CPT, SNOMED, HL7, FHIR).
• Proficiency with SQL, Python, and automation frameworks for data workflows.
• Hands-on experience integrating data from multiple healthcare systems and vendors .
• Knowledge of:
• Cloud-Based Solutions, for example: Amazon Web Services (AWS) with its healthcare-specific services, Microsoft Azure's healthcare cloud, and Google Cloud Healthcare
• APIs that provide scalable infrastructure for data storage, processing, and compliance with healthcare regulations, like HIPAA.
• Specialized Payer Platforms, such as Apixio, Veracyte and Health Catalyst.
• Enterprise Integration Platforms like Mulesoft, Informatica, and Talend.
• Excellent collaboration skills and ability to partner with AI/ML teams.
• Strong understanding of data governance, HIPAA compliance, and audit documentation .

• Study Risk Assessment: Conduct thorough risk assessments for clinical studies, identifying potential issues and developing mitigation strategies, in consultation with functional team leads and PM
• Centralized Statistical Monitoring: Perform centralized statistical monitoring & data analysis on study data to detect anomalies, trends, and potential risks, ensuring data accuracy and compliance.
• RBQM Meetings: support monthly RBQM meetings by supporting review of study data, documenting findings, action plans and coordination of data cleaning activities to support study deliverables
• Data Quality Assurance: Ensure the highest standards of data quality and integrity through proactive monitoring and timely interventions.
• Collaboration: Work closely with clinical operations, data management, biostatistics, and other departments to support proactive oversight and management and data cleaning for studies
• Reporting: Prepare detailed reports and presentations on monitoring activities, findings, and recommendations for sponsors and study teams.
• Operational Insights: Oversee operational study metrics, including data entry trends, SDV backlog, site health trending and proactively communicate issues to study team members to drive towards resolution & proactive remediation
  

• Bachelor’s Degree in a relevant field (life sciences, statistics, data management, clinical operations) or relevant/equivalent combination of education, training, and experience
• Minimum 2 years experience in clinical monitoring, clinical trial management or equivalent
• Working knowledge of ICH GCP guidelines and the clinical development process
  

• Highly effective oral and written communication skills with the ability to communicate effectively with project team members
• Excellent organizational and time management skills
• Excellent written and spoken English, including strong grammar and scientific vocabulary skills
• Ability to work in a team or independently as required
• Strong understanding of RBQM principles and methodologies.
• Demonstrated ability to learn how to extract pertinent information from protocols, electronic study data systems, clinical systems, dashboards, and to leverage these data to assess risk
• Proficiency in statistical analysis and data monitoring tools.
• Detail-oriented with strong analytical and problem-solving skills
  

• CRO experience as a Central Monitor
  

• Statistical analysis and data monitoring
• Risk assessment and mitigation
• Report writing and presentation
• Collaboration and teamwork
  

Live Medical Scribe Manager - 8AM - 5PM EST Time Zone

We’re seeking a Medical Scriber who is ready to work with new technologies and help our

providers with saving time and money. The ideal candidate has experience using the EHR

to scribe visitation notes into the patient’s chart while understanding the difference nuances between multiple providers in real time.

Objectives of this role

Responsibilities

• Reviews Physician dictation and transcribes to clinical notes in EMR/Billing systems

• Prepares and assembles medical record documentation/charts for physician(s).

• Ensures medical record compliance by self-documentation attestation.

• Updates patient history, physical exam, and other pertinent health information in the patient

• Prepares and sends all documentation to physicians for review and approval via authentication of detailed data entry and facility-specific procedures.

• Monitors the duration of basic lab results and screening procedures.

• Complies with hospital and medical facility policies, including those relating to HIPAA and Joint Commission.

• Performs other clerical duties and tasks to improve provider productivity and clinic workflow as assigned.

• Assign codes to diagnoses and procedures, using ICD (International Classification of Diseases) and CPT (Current Procedural Terminology) codes

• Ensure codes are accurate and sequenced correctly in accordance with government and insurance regulations

• Follow up with the provider on any documentation that is insufficient or unclear

• Communicate with other clinical staff regarding documentation

• Search for information in cases where the coding is complex or unusual

• Receive and review patient charts and documents for accuracy

• Review the previous day's batch of patient notes for evaluation and coding

• Ensure that all codes are current and active

Required skills and qualifications

• 3-5 years of experience as a Live Medical Scriber

• Administrative writing skills

• Reporting skills

• Organizational skills

• Record-keeping

• Microsoft Office skills

• Professionalism, confidentiality, and organization

• Typing

• Solid oral and written communication skills

• Education, Experience, and Licensing Requirements:

• Medical coding or successful completion of a certification program

• Bachelor’s degree with pre-health career track preferred

• Strong knowledge of anatomy, physiology and medical terminology

• Familiarity with ICD-X codes and CPT Procedures

• Skilled in operating various medical record software and hardware, word-processing, and database software programs

Role: Clinical Data Scientist / Trial Lead

Key Responsibilities

• Lead clinical data management activities across assigned clinical trials, ensuring high-quality data acquisition, database design, and data integrity.
• Act as a technical resource for Data Management (DM) and Risk-Based Monitoring (RBM) standards, tools, and reporting.
• Collaborate with cross-functional teams, external vendors, and internal stakeholders to ensure timely, compliant, and efficient data management processes.
• Ensure study-specific documentation is complete and maintained in the Trial Master File (TMF).
• Support data cleaning, integrity monitoring, e-data processing, and database release according to SOPs and industry best practices.

Qualifications

• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Clinical Research, or related field.
• 3+ years of experience in Clinical Data Management within the pharmaceutical or CRO industry.
• Strong knowledge of EDC systems, clinical trial processes, and regulatory compliance (ICH-GCP).
• Experience in Risk-Based Monitoring (RBM), data cleaning, and data visualization tools.
• Excellent analytical, communication, and problem-solving skills.

APPLICATION PROCESS

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Position: Health & Wellness Coach (100% Work from Home)

Experience: 5 Years Full-time in Fitness Industry

Salary: INR ₹60,000.00 - ₹75,000.00 per month (based on experience and qualifications)

Working Hours : Monday to Saturday, 8-9 hours per day.

Type: Full-time, Permanent

-- NO FRESHERS (OR INTERNS) ---

About Us:

We are a dynamic fitness start-up offering an Online Personal Training platform, TNV Method, that combines evidence-based fitness and nutrition coaching. Our holistic approach is designed to empower passionate fitness enthusiasts in achieving their health and wellness goals.

Why Join Us?

• Work from Home: Enjoy the flexibility of a 100% remote position.

• Impactful Role: Make a significant impact on clients’ lives by guiding them towards their fitness and health goals.

• Growth Opportunities: Continuous learning and professional development in a supportive environment.

• Competitive Compensation: Attractive salary based on your experience and expertise.

How to Apply:

Complete the assessment (Desktop only)

We are looking for dedicated, high-achieving individuals who are passionate about health and wellness. If you meet the qualifications and are ready to make a difference, apply now!

Essential Qualifications :

• MSc in Nutrition Science, Metabolic Disorders, and Meal Plan Development

• MSc Exercise Science, Strength & Conditioning, and Workout Programming

Experience:

• Minimum of 5 years in clinical and body transformations in full-time capacity.

Expectations and Responsibilities:

• Proficient in using Google Meet, Zoom, and email for seamless client and staff interactions.

• Always punctual and well-prepared for all sessions and meetings.

• Deep commitment to coaching individuals with a purpose, providing exceptional customer service.

• Ability to inspire and motivate clients towards their fitness and health goals.

• Dedicated to maintaining personal health, fitness, and professional ethics.

• Strictly follow all company protocols and policies.

• Actively engage in mandatory and optional staff training sessions.

• Effectively promote and sell personal training programs and services.

• Stay updated with the latest certifications and industry trends to deliver top-notch coaching.

Technical Areas of Expertise:

• Expertise in helping clients achieve their goals through meal planning, healthy recipes, supplement guidance, and balanced exercise routines.

• In-depth understanding of anatomy, functional exercise, basic nutrition, and exercise science.

• Exceptional service orientation with outstanding verbal and written English communication skills.

• Proficiency in designing tailored exercise programs and executing them safely and effectively.

• Capability to demonstrate exercises and provide constructive feedback on techniques.

APPLICATION PROCESS

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Location: Remote

Reports To: CEO / VP of RCM (U.S.-based)

Team Oversight: 25–40 offshore billers, AR callers, credentialing specialists, and auditors (India-based team)

The Director of RCM will provide strategic leadership and operational oversight for our offshore billing operations, ensuring end-to-end revenue cycle performance for U.S. healthcare provider clients. This leader will be responsible for building robust processes, maintaining payer compliance, driving collections, minimizing denials, and mentoring offshore teams to deliver world-class results.

• Define and execute the vision for RCM operations in alignment with company growth and client expectations.
• Develop policies, SOPs, and workflows that optimize revenue cycle performance across specialties (Orthopedics, Physical Therapy, Dermatology, Behavioral Health, Rheumatology, etc.).
• Partner with U.S. leadership to ensure client needs, compliance standards, and performance goals are consistently met.

• Oversee the daily operations of the billing team in India, including charge entry, payment posting, AR calling, denial management, credentialing, and reporting.
• Implement audit and QA frameworks to monitor accuracy, timeliness, and compliance.
• Standardize reporting cadence: daily, weekly, and monthly dashboards for AR, denials, collections, and payer trends.
• Ensure smooth onboarding of new clients and practices into billing workflows.

• Manage and mentor offshore managers, team leads, and billers to ensure accountability and career growth.
• Build a performance-driven culture with clear KPIs, evaluation frameworks, and feedback mechanisms.
• Drive recruitment, training, and upskilling initiatives to maintain high-quality output.

• Act as a bridge between U.S. leadership and offshore teams to ensure clear communication and alignment.
• Participate in client calls, providing updates on revenue performance, denial trends, and improvement initiatives.
• Proactively identify client risks and recommend process improvements.

• Ensure adherence to U.S. healthcare billing regulations, HIPAA compliance, and payer-specific requirements.
• Monitor payer changes, industry trends, and regulatory updates to update internal SOPs.
• Leverage technology and automation tools (e.g., practice management systems, RPA, reporting dashboards) to drive efficiency.

• Bachelor’s degree required; Master’s in Business, Healthcare Administration, or related field preferred.
• Minimum 8+ years of U.S. healthcare RCM experience , with at least 5 years in leadership roles overseeing offshore teams.
• Deep knowledge of the end-to-end RCM cycle (charge capture, claim submission, payment posting, AR follow-up, denial management, credentialing, patient collections).
• Proven experience managing teams of 30+ billers in India, Pakistan, or the Philippines.
• Strong understanding of U.S. payers, EHR/PM systems (e.g., Athena, eClinicalWorks, AdvancedMD, Kareo, Epic, DrChrono, Experity), and compliance frameworks (HIPAA, CMS).
• Excellent communication, leadership, and analytical skills.

• Strategic thinking and operational execution
• Strong analytical/reporting abilities (Excel, Power BI, or similar tools)
• Team leadership across multiple geographies
• Client management and presentation skills
• Problem-solving and process optimization

• AR Days: Maintain <35 days
• Clean Claim Rate: > 95%
• Denial Rate: <5%
• Collection Rate: > 95% of net collectible revenue
• Productivity: Calls/claims processed per FTE per day
• Team Performance: Adherence to SLAs and quality scores

Job Role: Ayurveda Consultant - Teleconsultation Services

Location : Bangalore (Bellandur) , 1 weeks training from office, Post training WFH.

About Kapiva Ayurveda: Kapiva Ayurveda is a pioneering wellness brand rooted in the ancient and holistic science of Ayurveda. We are committed to bringing traditional Ayurvedic wisdom through high-quality products and accessible health services.

Role Overview: We are seeking Ayurvedic doctors to join our dynamic teleconsultation team. As an Ayurvedic Doctor at Kapiva Ayurveda, you will be at the forefront of delivering expert Ayurvedic consultations, lifestyle advice, and personalized treatment plans to patients across the country via our digital platform.

This role is ideal for passionate Ayurvedic practitioners who are committed to leveraging their knowledge for the betterment of patient health while embracing tech to reach a wider audience.

Key Responsibilities:

• Conduct comprehensive online Ayurvedic consultations with patients, including diagnosis, treatment, Suggesting Investigations, and follow-up advice.
• Develop personalized treatment plans based on Ayurvedic principles, considering patient's health conditions and suggestive reports.
• Offer lifestyle and dietary recommendations under Ayurvedic practices to help patients achieve optimal health.
• Maintain accurate and detailed patient records in compliance with confidentiality and data protection laws
• Handling BAU responsibilities like ensuring Standard SOPs are followed.
• Participate in continuous learning and training to stay updated with the latest advancements in Ayurveda and telehealth for the benefit of the organization.
• Collaborate with the teleconsultation team and contribute to the development of the platform by providing insights and feedback.
• Assisting Market research teams with sharp insights into doctor <> patient consultation needs.

Requirements :

• B.A.M.S. degree from a recognized Ayurvedic college.
• Valid registration with a state or national Ayurvedic board/council.
• Minimum of 2 years of clinical experience in Ayurveda, with a strong understanding of Ayurvedic diagnostics and treatment protocols.
• Freshers can apply for a 3-round selection process which the team performs for young talents.
• Excellent communication skills, with fluency in English, Hindi, and at least one regional Indian language.
• Comfortable with using digital health platforms and technology for teleconsultation purposes.
• Strong interpersonal skills with the ability to empathize with patients and build trust.
• Self-motivated, with the ability to work independently and as part of a remote team.

What We Offer:

• The opportunity to be part of a leading Ayurvedic brand that is revolutionizing the wellness industry.
• A flexible and remote working environment, allowing you to consult from anywhere.
• Continuous professional development opportunities in Ayurveda and digital health.
• A supportive and collaborative team environment.
• Competitive compensation and incentives based on experience and performance.

How to Apply: If you are passionate about Ayurveda and possess the skills and qualifications we are looking for, please submit your application, including your resume at and why you are interested in this role

Kapiva Ayurveda is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all

Commitment: Full-Time Contract (30–40 hours per week)

Location: Based in India, Remote – Eastern Time Zone (preferred) or Mountain Time Zone

Reports To: Clinical QA Lead / Director of Quality

Position Overview

We are seeking an experienced QA Specialist / Manager-level contractor to provide day-to-day clinical quality assurance (QA) support across ongoing clinical trials. This individual will play a key role in guiding study teams, maintaining compliance with Good Clinical Practice (GCP) , and ensuring quality oversight. The ideal candidate brings strong experience with Veeva QMS , is highly tech-savvy, and can support clinical operations teams in a fast-paced, remote environment.

Key Responsibilities

• Serve as the primary QA support resource for clinical study teams, ensuring compliance with GCP and internal quality standards.
• Provide QA expertise during study calls, including:
• Protocol deviation meetings
• Risk-based quality management discussions
• Study operations and trial oversight meetings
• Write, review, update, and format standard operating procedures (SOPs) and other quality documentation.
• Manage and track quality processes within Veeva QMS , including document control, training, and CAPA management.
• Address QA-related questions from study teams in real time, providing clear and actionable guidance.
• Support inspection readiness and contribute to continuous improvement of QA systems and processes.
• Partner with cross-functional stakeholders (Clinical Operations, Data Management, Regulatory, etc.) to align on quality expectations and risk mitigation.

Qualifications

• Education: Bachelor’s degree in life sciences, healthcare, or related discipline (advanced degree preferred).
• Experience:
• 5+ years of Clinical Quality Assurance experience with a strong foundation in GCP.
• Prior experience supporting clinical study teams in a QA capacity.
• Hands-on experience with Veeva QMS .
• Technical Skills:
• Proficient in MS Office (Excel, PowerPoint, Word).
• Skilled in technical writing, SOP drafting, and document formatting.
• Soft Skills:
• Excellent communication and interpersonal skills.
• Strong organizational skills with the ability to work independently.
• Availability: Must be available during Eastern or Mountain Time Zone working hours to attend study calls and provide timely QA support.

Contract Opportunity

This is a full-time contract role offering 30–40 hours per week of consistent work. The contractor will act as a core member of the QA function, providing essential support to ongoing clinical programs and ensuring regulatory compliance.

Project role : Associate clinical lead

Work experience : 5 to 10 years.

Work location : Homebased.

Must have skills : Senior Clinical Research associate , CRA, Unblinded Monitoring, Onsite Monitoring.

Job overview : Unblinded Clinical Lead working as a oversight for global unblinded CRA team as well as providing technical support for Unblinded clinical operations.

Job Responsibility:

• Accountable for meeting projects’ recruitment targets and ensuring appropriate recruitment strategies are in place.
• Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project’s lifecycle.
• Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.
• Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.
• Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.
• Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.
• Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.
• May work as the Unblinded Clinical Lead on projects with 1-2 service lines and single/few countries or alongside more senior Clinical Leads to deliver large, global trials.;
• May attend site visits as applicable in support of project delivery.

Technical Skills :

• Requires 5+ years clinical research/monitoring experience or equivalent combination of education, training and experience
• Unblinded Monitoring experience preferred.
• Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.
• Requires basic understanding of project finances