ResponsibilitiesClinical Responsibility :To perform procedures independently as per privileges bestowed upon him or her as per hospital policy.To conduct in-patient round independently and with the respective junior consultants, and duty medical officers.To mention post-operative plan of care in the medical record.To supervise registrars and ensure that they discharge their duties in an effective and efficient manner.To verify the examination findings & medication orders written by the junior consultants and registrar.To impart relevant patient education as and when required.To mention date, time, name and signature against all entries in the medical record.To countersign any verbal order given to DMOs, junior consultants and registrars as and when needed.To prepare the ITU rota in coordination with the registrar on call.To take part in the patient management in the intensive care unit and hasten recovery and take steps to reduce ITU/Step down ICU/Hospital stay.To attend to patient’s complaints reported by the registrars or nursing staff as & when required.To give orders for discharge as per the patients conditions & intimate the registrar / resident to do the needful.To attend to all emergencies while on call.To impart training to the residents & registrars.To abide by the policies & procedures of the Hospital.To help ensure compliance with Quality standards & closure of the non-conformities.Research :Conduct medical research to aid in controlling and curing disease, to investigate new medications, and to develop and test new medical techniques.To be a thesis guide for fellows, residents and PhD candidates.Administrative:Coordinate and direct work of nurses, medical technicians and other health care providers.Inform students and staff of types and methods of Cardiac Intervention administration, signs of complications, and emergency methods to counteract reactions.Manage Cardiac Services, coordinate with other medical activities and formulate plans and procedures.Teaching:Must take part in the ongoing teaching activities.Organize workshops, seminars, conferences at local, regional and national level

Responsibilities• Assist in establishing and implementing goals, objectives, policies, procedures and systems.• Gather and report fiscal, statistical and analytical data including audit compliance.• Assist in developing cost-effective administrative and operational policies.• Plan and coordinate daily work assignments and operations.• Resolve administrative and operational issues and escalate appropriately.• Ensure compliance with regulations and standards.• Work with medical staff to ensure quality patient care and confidentiality.• Prepare duty rosters for staff.• Participate in quality improvement initiatives and protocols.• Ensure operational quality and patient safety.• Support smooth functioning and overall performance of the hospital.Qualification & Experience•  Work Experience 10+ years• Qualification BHMS/BAMS/MBBS/MBA/ MHA

Responsibilities Coordinate with Principal Investigators (PIs), Institutional Review Boards (IRB), Sponsors/CROs, and research teams to execute clinical trials. Recruit and follow up with trial participants to ensure their well-being throughout the study. Maintain trial databases, logs, and documentation for regulatory compliance. Ensure adherence to Good Clinical Practice (GCP) guidelines and applicable regulatory requirements. Train staff on trial-related duties and ethical considerations in clinical research. Protect the rights and confidentiality of all trial participants. Ensure timely and accurate reporting of trial data, including adverse events and protocol deviations. Manage documentation, including informed consent forms, Case Report Forms (CRFs), and other regulatory submissions. Archive trial-related documents for the required retention period. Identify potential research opportunities and liaise with sponsors.  QualificationBachelors/Masters in Life Sciences w/ Certificate course in Clinical Research, OR Bachelors/Masters in Clinical Research Excellent written and oral communication skills. Preference for ICH-GCP trained professional.

Qualification & Experience           Experience Required : Fresher/Experienced     Qualification Required : BAMS                   

Responsibilities Evaluates medical information against criteria, benefit plan, coverage policies and determines necessity for procedure and refers to Medical Director if criteria are not met Evaluate itemized bills against reimbursement policies Adheres to quality assurance standards Serves as a resource to facilitate understanding of products Handles some escalated cases; secures supervisory assistance with problem solving and decision making Advises supervisory staff of any concerns or complaints expressed by Health Care Professionals Utilizes effective communication, courtesy and professionalism in all interactions, both internally and externally Performs additional unit duties below as appropriate: Participate on special projects. Perform random or focused reviews as required. Support and assist with training and precepting as required Analyze clinical information Perform claim reviews with focus on coding and billing errors Identify and refer cases for possible fraud/abuse or questionable billing practices to the appropriate matrix partners Handle multiple products and benefit plans Works under moderate direct supervision Qualification & ExperienceMBBS Maintain active Medical as required by state and company guidelines Clinical experience in hospital/clinic for 3 or more years Team player Flexible/Adaptable Excellent time management, organizational, and research skills Experience with MS Office Suite (Outlook, Excel, Access, SharePoint)

Responsibilities People Leadership & Capability Management Provide direct line management to: Data Integration Developers Quality Auditors – Provider Data Quality Provider Data Admin Assistants Set clear objectives, performance expectations, and development plans aligned to Data Enablement strategy. Coach, mentor, and upskill team members, ensuring strong technical capability, quality mindset, and role clarity. Manage capacity planning and work allocation across teams to meet changing business priorities. Lead performance interventions where required, including quality remediation, coaching plans, and escalation.  Operational Delivery & Oversight Own end-to-end delivery of provider data cleansing, validation, audit, and bulk update activities. Ensure adherence to documented operating procedures, controls, and data governance standards. Monitor delivery against agreed SLAs, turnaround times, and quality thresholds. Act as the primary escalation point for complex data issues, bulk update risks, or audit failures. Ensure appropriate segregation of duties between data execution, validation, and audit activities.  Data Quality, Audit & Control Embed robust quality assurance and audit frameworks across provider data activities. Review audit findings, trends, and root cause analysis; ensure corrective actions are defined and implemented.

ResponsibilitiesConducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Qualification & ExperienceBachelor's degree in a scientific or healthcare-related field. Minimum of 3 years of experience as a Clinical Research Associate & On-Site Monitoring In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Oncology/Immunology TA is mandatory Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment.

ResponsibilitiesTo effectively review visit reports as per Protocol and ICON and Sponsor SOPs and to ensure the quality of reports are of the highest standards , errors are minimized and that issues are escalated as appropriate To follow up on action items and protocol deviations and to be a liaison between CRA, CTM and PM for timely resolution of issues. To act as an extension of the CTM/CTM team for the specific purpose of visit report review and approval. To observe and escalate safety trends in patients as identified in visit report Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance . As a Manager, the employee is expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs. Effectively review and approve visit reports as per annotated report, protocol, ICON and/or Sponsor SOPs and ensure errors are minimized , reports are consistent across visits and sites and adhere to the highest standards of quality . Ensure turnaround time of the visit reports per contract, ICON and or Sponsor SOPsQualification & ExperienceBachelor’s degree in life sciences, healthcare, or a related field (advanced degree preferred). Minimum 8-10 years of Clinical Research experience with at-least 5 years of on-site monitoring experience. Experience in On-Site Monitoring and Clinical Trial Management, with a solid understanding of on-site monitoring approaches. Strong analytical skills with proficiency in clinical trial data review and interpretation. Excellent organizational and project management skills, with the ability to manage multiple studies and meet deadlines. Effective communication and interpersonal skills, with the ability to collaborate across diverse teams and functions.

ResponsibilitiesReview & Verification: Check patient demographics, insurance eligibility, benefits, and coverage for specific medical procedures or medications. Submission to Insurance: Prepare and submit authorization requests with complete clinical documentation (e.g., medical necessity) to insurance companies. Communication & Follow-Up: Act as a liaison, contacting providers for more info and following up with insurers on pending approvals. Documentation: Accurately log all communications, authorization numbers, and outcomes in the system, adhering to HIPAA.  Qualification & Experience5+ years experience working in US Healthcare Pre-authorization / Benefit check Strong attention to detail and organizational skills. Excellent communication (written and verbal) and interpersonal abilities. Knowledge of medical terminology and healthcare coding (e.g., CPT, ICD-10). Familiarity with HIPAA regulations and insurance policies. Proficiency with Salesforce and EHR software. Ability to work efficiently under pressure, meeting turnaround times.

ResponsibilitiesEnsures that all allocated projects are carried out in strict accordance with the relevant protocols, global harmonized SOPs, and the specified standards of GCPs. Demonstrates capability to read and follow study timelines for on-time deliverables. Potential to assist with inputs on study design or capable to make suggestions to study timelines when warranted. Assist with review of clinical trial data in accordance with Data Management Plans and/or Data Review Guidelines and raise queries to resolve erroneous, missing, incomplete data. Run and execute additional programs (special listings, reconciliation discrepancy listings, etc.) used to support the review of clinical trial data. Generate, resolve and track queries to address problematic data identified during aggregate data review activities. Interacts with other project team members to support the set-up, maintenance, and closure of the Data Management aspects of the project and attend meetings as required. Generate and QCs data listings for internal data review. May assist or create dummy data to test edit checks and to test database screen design and functionality. Assist or create dummy data to test SAS reports and data listing. Demonstrates the ability to review Edit Check Specifications and Database specifications. Post Data Management documentation and data management related administrative tasks as requested, including maintenance of eTMF as required. Runs study status reports in preparation for Sponsor meetings and to deliver on specific Sponsor request. Assist with the completion of Database Lock and Unlock activities. Supports the training of new staff on project specific Data Management processes. Performs any other duties as assigned.Qualification & ExpeirenceUniversity / college degree (life sciences, health sciences, information technology or related subjects) or a certification in allied health professions from an appropriate accredited institution. Fluent in English, both written and verbal. Experience (Minimum Required): 3 to 5 years of relevant work experience with increasing responsibility in data management with knowledge of one (1) or more therapeutic areas. Demonstrated time management skill and ability to adhere to project productivity metrics and timelines. Knowledge of medical terminology is preferred. Knowledge of effective clinical data management practices.