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Role & Responsibilities • Diagnose and treat a wide range of dermatological conditions and skin diseases • Perform comprehensive skin evaluations and review medical histories • Develop and implement personalised treatment plans • Provide dermatology consultations and follow-up care • Perform dermatological procedures including biopsies, excisions, and minor surgeries • Prescribe and administer treatments such as topical and oral medications, laser therapy, cryotherapy, and phototherapy • Deliver cosmetic dermatology services including Botox, dermal fillers, chemical peels, and laser treatments • Educate patients on skincare routines, preventive care, and treatment adherence • Maintain accurate and compliant patient medical records • Stay updated with the latest dermatology advancements through continuous medical education • Collaborate with multidisciplinary healthcare teams for comprehensive patient care • Ensure a safe, sterile, and professional clinical environment Qualification • Doctor of Medicine (MD) or equivalent from a recognised institution Experience • Minimum 3 years of clinical experience in dermatology • Experience in both medical and cosmetic dermatology preferred License / Registration • Valid Abu Dhabi medical license or eligibility to obtain one Skills • Strong clinical expertise in dermatology • Proficiency in dermatological and aesthetic procedures • Excellent communication and patient interaction skills • Ability to manage diverse patient cases independently • Attention to clinical quality, safety, and compliance Language • English – fluent • Arabic – advantageAbout the Company The organisation is a well-established and reputed healthcare facility in Abu Dhabi, delivering high-quality medical and aesthetic dermatology services.

Role & Responsibilities • Conduct comprehensive product induction sessions for new employees • Plan, organise, and deliver internal training on product knowledge (theoretical and practical) • Provide continuous education on product usage and patient care techniques • Coordinate and manage hospital workshops, training programs, and awareness activities • Develop and maintain monthly activity and training calendars • Track and monitor activities across territories to ensure timely execution • Collect, analyse, and report data post workshops and training events • Develop, update, and enhance training materials and learning modules • Track newly generated leads and ensure appropriate follow-up • Oversee and guide teams handling patient and caregiver communication • Share field insights to support product improvement and new product development initiatives Qualification • B.Sc Nursing or M.Sc Nursing Experience • Clinical training or patient care experience preferred • Exposure to product training or medical devices is an advantage Mandatory Certification • Enterostomal Therapy Nurse (ETN) qualification Skills • Strong presentation and communication skills • Training and facilitation expertise • Good understanding of nursing and patient care practices • Ability to manage field activities independently • Analytical skills for activity tracking and reporting • Willingness to travel extensively Work Location • On-site – Hyderabad, Telangana About the Company • Colostocare Pvt Ltd specialises in patient-focused medical care solutions, Committed to improving quality of life through clinical education and product innovation

Role & Responsibilities • Contribute to a culture of process improvement and operational excellence • Review and process Serious Adverse Events (SAEs), spontaneous ADRs, and safety data • Perform safety review of clinical and diagnostic data • Ensure case processing accuracy as per SOPs, study procedures, regulatory and sponsor requirements • Maintain and review safety tracking systems for data quality and compliance • Liaise with investigational sites, reporters, sponsors, and cross-functional teams on safety issues • Attend project team meetings and sponsor teleconferences as required • Serve as a safety resource for investigational sites and internal teams • Assist in training and mentoring junior Drug Safety Associates • Support generation of study-specific procedures and identify out-of-scope activities • Act as Lead Drug Safety Associate for local or regional projects • Support MSS Functional Lead under supervision • Travel up to 10% (domestic/international) as required Qualification • Life Sciences / Pharmacy / Healthcare background preferred Experience • 4–10 years of experience in Pharmacovigilance / Drug Safety • Experience in Pharma, Biotech, CRO, or Clinical Research environments Skills • Strong knowledge of Pharmacovigilance processes • Hands-on experience with Oracle Argus • Knowledge of EudraVigilance and global safety databases • Exposure to aggregate reporting activities • Strong attention to detail and data quality focus • Effective communication and stakeholder coordination skills • Ability to work independently and lead safety activities About the Company • Covalent Trainings specialises in pharmacovigilance training and industry placements, Supports global PV projects across pharma, biotech, and CRO sectors

Roles & Responsibilities: • Ensure MAH pharmacovigilance compliance with EU GVP Modules and UK MHRA requirements • Act as operational PV representative for UK and EU markets • Support QPPV / UK QPPV in maintaining PV system oversight • Ensure PV agreements with partners, distributors, and service providers are in place • Provide oversight of outsourced PV providers (ICSRs, literature, signals, aggregate reports) • Monitor vendor performance against KPIs and SLAs and lead governance meetings • Ensure timely and compliant ICSR reporting to EudraVigilance, MHRA, and partners • Oversee PSUR/PBRERs, RMPs, signal management, and benefit–risk evaluations • Maintain MAH PV Quality Management System and ensure SOP compliance • Support PV inspections and audits (MHRA, EMA, partners) and manage CAPAs • Act as PV contact for Regulatory, Quality, and Commercial teams • Ensure safety information is accurately reflected in SmPC, PIL, and submissions Qualifications: • M.Pharma in Pharmacy Experience: • Proven pharmacovigilance experience within UK and/or EU • Experience working in an MAH environment • Hands-on experience managing outsourced/third-party PV providers Skills: • Strong regulatory and compliance mindset • Excellent vendor and stakeholder management skills • Strong documentation, review, and inspection readiness abilities • Ability to work independently and manage multiple priorities • Experience in generics and post-marketing PV • Exposure to global PV operations and EudraVigilance systems About the Organization: B&S Group is a global distribution and supply chain organization operating across pharmaceuticals and healthcare, with a strong focus on regulatory compliance, quality, and patient safety across international markets.

Role & Responsibilities • Assist in diagnosis and management of patients under assigned departments • Provide inpatient and outpatient clinical services as per institutional protocols • Support senior residents and consultants in patient care and procedures • Maintain accurate medical records and clinical documentation • Participate in ward rounds, academic activities, and clinical discussions • Ensure adherence to hospital policies, ethics, and patient safety standards Qualification Name of the PostsNo.of VacanciesQualificationJunior Resident 06MBBS, MD/MS  Experience • Freshers and eligible postgraduates may apply • Relevant clinical exposure preferred Age Limit • Minimum: 21 years • Maximum: 30 years • Age relaxation as per government rules Selection Process • Walk-in Interview Application Fee • No application fee How to Apply • Check the Junior Resident Recruitment 2026 notification • Verify eligibility criteria • Attend the walk-in interview at the venue mentioned below Walk-in Venue • Office of the Head, Clinical Hematology & Medical Oncology • PGIMER, Chandigarh • Room No. 18, Block-F, 4th Floor, Nehru Hospital Application Date • Walk-in Interview Date: 03-02-2026 About the Organisation • PGIMER is a premier medical education and research institute in India , Known for excellence in clinical care, research, and postgraduate trainingOfficial NotificationClick Here

Roles & Responsibilities: • Report safety information from India and India cluster (South Asia countries) to Global Safety • Follow up with reporters for additional safety information • Review and manage safety mailbox for incoming reports • Perform monthly reconciliation and compliance checks from a pharmacovigilance perspective • Prepare and submit Periodic Safety Update Reports (PSURs) to regulatory authorities as per regulations • Gather requirements and prepare regulatory dossiers for new products, clinical trials, variations, and renewals • Prepare responses to regulatory authority queries and coordinate with global teams • Support preparation for regulatory authority and expert committee meetings • Prepare and follow up on regulatory submissions for South Asia countries • Prepare and update product labeling materials • Review promotional materials for compliance with approved product registrations • Ensure timely updates to regulatory databases • Update and maintain local SOPs • Update and renew safety agreements with partners, manufacturers, and distributors • Coordinate price updates and ensure timely entry into NPPA pricing database • Manage lifecycle maintenance activities and update commercial teams on key milestones Qualifications: • Bachelor’s degree in Pharmacy, Life Sciences, Microbiology, Chemistry, or related field Experience: • Minimum 1+ year experience in India Regulatory Affairs and Pharmacovigilance • Experience within pharmaceutical or biotechnology industry preferred Skills: • Knowledge of Indian regulatory and pharmacovigilance requirements • Strong documentation and dossier preparation skills • Ability to coordinate with global and cross-functional teams • Good communication and regulatory compliance understanding • Attention to detail and ability to manage multiple submissions About the Organization: Ferring Therapeutics is a global, research-driven biopharmaceutical company committed to developing innovative treatments in areas of high unmet medical need. The company focuses on maintaining the highest standards of quality, regulatory compliance, and patient safety while delivering life-changing therapies worldwide.

Roles & Responsibilities: • Perform medical assessments of client’s product ranges and evaluate adverse events • Conduct medical reviews of aggregate reports and prepare clinical expert statements • Detect signals for client’s medicinal products and manage risk management plans • Provide guidance and participate in follow-up of adverse events, offering backup medical support • Interact with staff at various levels to resolve issues during reviews • Contribute to enhancing pharmacovigilance processes and writing SOPs • Ensure compliance with local regulations and global pharmacovigilance requirements • Assist in developing SOPs for the department and clients, and communicate with clients and regulatory agencies if needed Qualifications: • Relevant degree in Life Sciences, Pharmacy, or related field Experience: • 0–1 year in pharmacovigilance or related field Skills: • Knowledge of local and national pharmacovigilance requirements • Strong communication and client interaction skills • Ability to work effectively with staff at various levels and functional areas • Marketing, business generation, direct sales, and client servicing skills About the Organization: This organization is a dynamic employment and recruitment services firm providing specialized healthcare and pharmacovigilance staffing solutions. They focus on regulatory compliance, quality processes, and client satisfaction while fostering a collaborative environment for professional growth.

Roles & Responsibilities: • Prepare and review clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and other clinical trial documents in line with regulatory guidelines and industry standards • Collaborate with cross-functional teams, including clinical operations, regulatory affairs, and biostatistics, to ensure accuracy and completeness of deliverables • Interpret and summarize clinical trial data from study reports, statistical analyses, and scientific literature • Assist in preparation of regulatory submissions (INDs, NDAs, BLAs, MAAs) with high-quality medical writing support • Participate in project meetings, provide updates on medical writing activities, and contribute to project planning and timelines • Stay current with developments in medical writing, regulatory requirements, and therapeutic areas relevant to projects • Mentor junior medical writers and provide guidance on best practices for document preparation Qualifications: • Bachelor’s degree in Life Sciences, Pharmacy, or related field; advanced degree (MD, PhD, PharmD) preferred Experience: • Minimum 5 years of experience in medical writing within pharmaceutical, biotechnology, or CRO industry • Proficiency in interpreting clinical trial data, including statistical analyses and safety reports • Strong understanding of regulatory guidelines (ICH, FDA, EMA) for clinical trial documents and submissions Skills: • Excellent written and verbal communication skills • Detail-oriented with strong organizational and time management abilities • Ability to work independently and collaboratively in multidisciplinary teams • Proficiency in Microsoft Office Suite and familiarity with document management systems (e.g., SharePoint) About the Organization: MS Clinical Research Pvt Ltd is a dynamic and innovative clinical research organization specializing in clinical trials and comprehensive medical writing services. The company is committed to advancing medical research, supporting regulatory submissions, and improving patient outcomes through high-quality, scientifically accurate documentation and collaborative project execution.

Roles & Responsibilities: • Conduct site initiation, routine monitoring, and close-out visits to ensure compliance with study protocols, GCP, and regulatory requirements • Build and maintain strong relationships with investigative sites, investigators, and study coordinators • Perform routine monitoring visits to assess site performance, data integrity, and regulatory compliance • Ensure timely resolution of data queries and issues identified during monitoring visits • Ensure all study activities are conducted according to approved protocols, SOPs, and regulatory guidelines • Collaborate with investigators to address and resolve protocol-related queries • Assist in preparation and submission of regulatory documents to ethics committees and regulatory authorities • Collaborate with data management teams for accurate and timely data collection and entry • Perform source data verification and data validation activities • Monitor and report adverse events as per regulatory and safety reporting procedures • Provide training and support to site staff on study protocols, data collection, and regulatory compliance • Act as a resource for investigators and site staff throughout the study Qualifications: • Bachelor’s degree in Life Sciences or a related field Experience: • Minimum 3 years as a Clinical Research Associate with proven site management and monitoring experience • Familiarity with regulatory requirements and guidelines governing clinical trials Skills: • Excellent verbal and written communication skills • Strong organizational and time management skills with attention to detail • Ability to work effectively in cross-functional teams and independently • Willingness to travel to investigative sites as required About the Organization: MS Clinical Research Pvt Ltd is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. The company focuses on conducting high-quality clinical trials, ensuring regulatory compliance, and supporting the development of innovative medical solutions in a collaborative and dynamic environment.

Role & Responsibilities • Provide overall clinical oversight and administrative leadership for addiction treatment services • Formulate, review, and implement organisational healthcare policies, procedures, and ethical standards • Oversee all clinical services, ensuring alignment with evidence-based addiction treatment practices • Ensure safe and compliant use of controlled medications • Provide direct psychiatric or medical care to a limited caseload of patients • Integrate behavioural health, addiction services, and medical care for comprehensive treatment delivery • Lead quality improvement, patient safety, and risk management initiatives • Analyse clinical data, outcomes, and participate in peer review processes • Mentor, guide, and supervise medical staff including psychiatrists, physicians, and clinical directors • Collaborate with the CEO and executive leadership on strategic planning and execution • Oversee recruitment, training, performance management, and professional development of clinical teams • Ensure compliance with local regulations and international accreditation standards (e.g. Joint Commission) • Act as the primary liaison between administration, medical staff, regulators, insurers, and external stakeholders • Manage medical department budgets, resources, and inventory efficiently Qualification • Western-trained Consultant Psychiatrist (Addiction) • Recognised postgraduate qualification in Psychiatry • Eligible for senior leadership and clinical practice in the UAE Experience • Minimum 15 years’ experience in addiction treatment or behavioural health • Mandatory prior experience in a C-suite leadership role (Chief Medical Officer or equivalent) • Experience leading large drug & alcohol rehabilitation facilities essential Skills • Strong clinical leadership and strategic decision-making skills • Deep expertise in addiction psychiatry and rehabilitation medicine • Proven ability to lead multidisciplinary clinical teams • Strong governance, compliance, and accreditation knowledge • Excellent stakeholder engagement and executive communication skills • High ethical standards and patient safety focus About the Opportunity • Senior executive role in a cutting-edge addiction rehabilitation centre, Opportunity to shape clinical strategy and quality of care at an organisational level

Roles & Responsibilities: • Conduct clinical trials as per ICH-GCP guidelines, study protocols, and SOPs • Operate, handle, and maintain lab instruments as per SOPs and manuals • Document instrument data accurately and maintain calibration records • Perform routine instrument calibration and ensure proper record keeping • Coordinate with floor teams to ensure smooth execution of study activities • Assist in scheduling study subjects and ensure adherence to timelines • Submit study-related data on time for analysis • Report deviations, anomalies, or concerns to line manager and escalate when needed Qualifications: • Bachelor’s degree or diploma in Life Sciences, Pharmacy, or related field Experience: • Prior experience in clinical research or laboratory environment preferred Skills: • Knowledge of ICH-GCP and clinical trial procedures • Strong attention to detail and documentation accuracy • Good communication and coordination skills • Ability to work collaboratively in a fast-paced research environment About the Organization: MS Clinical Research Pvt Ltd is a leading clinical research organization focused on conducting high-quality clinical trials. The company is committed to maintaining international standards, ensuring data integrity, and supporting innovative healthcare solutions.

Role & Responsibilities • Perform signal detection activities across global safety databases • Conduct medical review and assessment of aggregate safety reports (PSUR, PBRER, DSUR) • Perform medical evaluation of Individual Case Safety Reports (ICSRs) • Support benefit–risk evaluation and safety decision-making • Ensure compliance with global pharmacovigilance regulations and guidelines • Collaborate with pharmacovigilance, regulatory, and cross-functional teams • Maintain high standards of documentation and medical review quality Qualification • MBBS or MD (mandatory) • Registered medical practitioner in India Experience • Minimum 1 year of experience in pharmacovigilance or drug safety • Hands-on exposure to signal detection and aggregate reporting preferred Skills • Strong knowledge of signal detection methodologies • Experience with aggregate safety reports (PSUR, PBRER, DSUR) • Understanding of global PV guidelines (ICH, GVP) • Good analytical and medical writing skills • High attention to detail and compliance orientation Availability • Immediate joiners or candidates with up to 1 month notice period preferred About the Company • OrciMed Life Sciences is a growing pharmacovigilance and life sciences services organisation

Role & Responsibilities:• Provide general dental care and treatment to patients• Perform routine dental procedures including diagnosis, cleaning, fillings, and minor surgeries• Assess patients’ oral health and recommend appropriate treatment plans• Maintain accurate patient records and documentation• Deliver patient care with professionalism and a commitment to quality• Collaborate with the dental team to ensure smooth clinic operationsQualifications:• Bachelor’s degree in Dentistry (B.D.S) from a recognized institutionExperience:• 1–2 years of relevant experience preferred (Freshers can also apply)Skills:• Patient assessment and diagnosis• Medical documentation and record keeping• Strong communication and interpersonal skills• Commitment to learning and professional growthAbout the Company:Rootz Dental, Bengaluru, is a professional dental clinic group dedicated to providing high-quality dental care. The clinic focuses on patient-centric treatments, continuous professional growth, and a supportive environment for both freshers and experienced dental professionals.

Roles & Responsibilities: • Develop, program, and validate ADaM datasets as per CDISC standards. • Create Tables, Listings, and Figures (TLFs) using SAS and/or R. • Implement Statistical Analysis Plans (SAP) and Statistical Programming Plans (SPP). • Ensure compliance with regulatory and industry standards (CDISC – SDTM, ADaM). • Collaborate closely with biostatisticians and clinical teams to ensure data accuracy. • Develop reusable macros and automate programming processes for efficiency. • Perform independent QC checks on statistical outputs and deliverables. • Support programming activities across multiple therapeutic areas including Oncology, Neuroscience, and Immunology. Qualifications • Graduate / Postgraduate in Life Sciences, Engineering, Statistics, or related disciplines.Experience: • 3 to 12 years of experience in clinical or biostatistical programming. • Hands-on experience in ADaM, TLF development, and clinical trial data analysis. Skills: • Strong expertise in SAS and/or R programming. • In-depth knowledge of CDISC standards (SDTM, ADaM). • Experience working with clinical trial protocols and regulatory guidelines. • Proficiency in TLF generation and data manipulation techniques. • Strong analytical, problem-solving, and attention-to-detail skills. • Exposure to additional tools such as Python or SQL (preferred). • Basic understanding of machine learning concepts applied to clinical data (preferred). About the Organisation: The organization is a leading clinical research and data analytics-driven company supporting global clinical trials across multiple therapeutic areas, offering a collaborative work environment, exposure to regulatory-compliant projects, and long-term career growth opportunities in statistical and clinical programming.

Role & Responsibilities:Dental Care• Perform diagnosis, restorations, RCTs, extractions, crown & bridge• Handle routine OPD and dental emergencies• Maintain sterilization and clinic safety protocols• Provide treatment counselling, post-care advice, and follow-upsAesthetic Procedures• Perform Hair & Skin treatments: HydraFacial, Chemical Peels, PRP/GFC, Laser Hair Removal, Acne/Pigmentation care, Anti-Aging facials• Customize session plans based on patient needs• Track improvements and maintain case files with before/after recordsClinic & Patient Handling• Deliver smooth patient experience and educate patients about procedures• Work with front desk and tele-calling team for patient conversions• Maintain documentation, consent forms, and treatment reviewsQualifications:• BDS / MDS with Aesthetic Certification• 0–5 years experience (Freshers with training also considered)• Skills: RCT, Cosmetic Dentistry, Dermal Procedures• Certification in Aesthetic Medicine (Preferred & mandatory)Skills Required:• Strong patient communication and interpersonal skills• Confidence in diagnosis and clinical procedures• Attention to detail and ability to handle dental & aesthetic cases ethicallyBenefits:• Opportunity to practice in a multi-specialty clinic setup• Hands-on training in advanced dental & aesthetic systems• Growth towards Senior Doctor / Branch Head roles• Attractive salary plus performance incentivesSchedule:• Day shift• Weekend availability (weekly off provided)About the Company:H-CURA PVT LTD is a multi-specialty clinic in Guntur focused on providing high-quality dental and aesthetic treatments. The clinic emphasizes patient-centric care, clinical excellence, and ethical practices. With a team of skilled professionals and advanced treatment technologies, H-CURA aims to deliver exceptional dental care along with comprehensive aesthetic solutions, offering opportunities for career growth and hands-on learning.

Role & Responsibilities:• Meet patients to assess dental concerns and explain treatment options• Perform regular dental check-ups, cleaning, and preventive dental procedures• Carry out basic dental procedures as per clinical standards• Establish and guide patients on effective oral hygiene and dental care plans• Maintain accurate patient records and medical documentation• Coordinate and communicate with clinic staff to ensure quality patient care• Deliver patient-centric care with strong interpersonal interactionQualifications:• Bachelor’s degree in Dental Surgery (BDS)Experience:• Freshers and experienced candidates are welcome• Strong communication and interpersonal skills are mandatorySkills Required:• Patient assessment and case understanding• Knowledge of medical terminology and dental procedures• Good communication and patient-handling skills• Ability to work collaboratively in a clinical team• Professional attitude and willingness to learnBenefits:• Flexible work scheduleAbout the Company:Apollo Dental Clinic – Ambattur is a trusted dental care provider offering comprehensive dental treatments with a focus on patient comfort, ethical practice, and clinical excellence. The clinic provides an encouraging environment for both freshers and experienced dentists to grow professionally.

Roles & Responsibilities: • Manage day-to-day medical coding operations. • Assign accurate diagnosis and procedure codes to patient charts. • Maintain a minimum of 95% quality on production. • Adhere to internal and external coding compliance policies and client requirements. • Improve performance based on feedback from reporting managers. • Follow organizational policies related to information security, HIPAA, and HR compliance. Qualification: • Life Science or Paramedical graduate. • No backlogs with complete academic documentation. Skills: • Strong analytical and logical thinking skills. • High attention to detail and accuracy. • Average written and spoken English communication skills. • Ability to understand medical terminology and coding standards. Assessment / Interview Process: • HR Interview. • Online Assessment – Anatomy & Physiology. • Medical Transcription (MT) Training. • MT-cleared candidates will be onboarded into Medical Coding training batch. Compensation & Benefits: • Competitive remuneration. • Annual performance-based bonus. • Standard industry benefits. • Relocation package as per company policy (for candidates outside base city). About the Organisation: AGS Health is a global leader in healthcare revenue cycle management, combining AI-enabled technologies with expert services to support leading U.S. health systems, physician groups, and academic medical centers, with 12,000+ professionals serving 100+ clients worldwide.

Role & Responsibilities • Build and maintain peer-level scientific relationships with Neuroscience KOLs • Drive high-quality scientific discussions across Parkinson’s disease, Multiple Sclerosis, migraine, and related indications • Support upcoming product launches, CMEs, and advisory board meetings • Conduct compliant scientific exchange with neurologists and HCPs • Generate actionable medical insights from field interactions • Collaborate cross-functionally with Medical Affairs, Marketing, and Commercial teams • Contribute to medical strategy execution and launch readiness Qualification • MBBS / BDS / PharmD / MSc / PhD Experience • 1–2 years’ experience in Medical Affairs or MSL roles • Neuroscience therapeutic experience preferred Skills • Strong scientific communication and presentation skills • Ability to engage neurologists and senior clinicians in scientific dialogue • Good understanding of clinical data and treatment paradigms • Self-driven and capable of working independently in the field • Willingness to travel within assigned territories Why Join • Opportunity to work with an innovation-driven neuroscience portfolio • Early exposure to launch excellence and strategic medical affairs activities • Direct impact on patient care through scientific engagement • Strong platform for long-term growth in Medical Affairs and leadership roles

Roles & Responsibilities: • Manage day-to-day medical coding operations. • Assign accurate diagnosis and procedure codes to patient charts. • Maintain a minimum of 95% quality on production. • Adhere to internal and external coding compliance policies and client requirements. • Improve performance based on feedback from reporting managers. • Follow organizational policies related to information security, HIPAA, and HR compliance. Qualification: • Life Science or Paramedical graduate. • No backlogs with complete academic documentation. Skills: • Strong analytical and logical thinking skills. • High attention to detail and accuracy. • Average written and spoken English communication skills. • Ability to understand medical terminology and coding standards. Assessment / Interview Process: • HR Interview. • Online Assessment – Anatomy & Physiology. • Medical Transcription (MT) Training. • MT-cleared candidates will be onboarded into Medical Coding training batch. Compensation & Benefits: • Competitive remuneration. • Annual performance-based bonus. • Standard industry benefits. • Relocation package as per company policy (for candidates outside base city). About the Organisation: AGS Health is a global leader in healthcare revenue cycle management, combining AI-enabled technologies with expert services to support leading U.S. health systems, physician groups, and academic medical centers, with 12,000+ professionals serving 100+ clients worldwide.