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3.0 - 7.0 years

0 Lacs

haryana

On-site

You will be leading the launch and day-to-day operations of Everhope Oncology's clinics in the city. From infrastructure and staffing to doctor engagement and patient experience, you will own every aspect of center performance. This is a high-impact, execution-focused role at the frontlines of scaling accessible cancer care across India. Your responsibilities will include setting up and launching new clinics/daycare centers, managing all aspects of center readiness such as infrastructure, design equipment, staffing, and supplies. You will lead clinic operations to ensure efficient processes, optimal resource utilization, and financial oversight. Implementing and monitoring Standard Operating Procedures (SOPs) to maintain high standards of care, safety, and service delivery will be crucial. Building and maintaining strong relationships with doctors and healthcare professionals/providers, ensuring effective communication and coordination with medical teams to support patient care and clinic growth will be part of your role. You will also oversee all aspects of the patient journey to ensure a superior patient experience, implementing strategies to enhance patient satisfaction, address concerns, and promote a culture of empathy and patient-centric care. To excel in this role, you should have 3-6 years of experience in hospital management, healthcare operations, or a related field. Preferred candidates will have experience in setting up or managing healthcare facilities/clinics and possess in-depth knowledge about clinical operations. Strong interpersonal and communication skills are essential, along with the ability to build and maintain relationships with healthcare providers. Strategic thinking, problem-solving skills, experience in driving digital initiatives, and managing revenue targets will be advantageous for this position.,

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5.0 - 9.0 years

0 Lacs

noida, uttar pradesh

On-site

As the Director - Clinical Services at Clinitech India, you will be responsible for shaping the clinical strategy, operations, and customer success of the healthcare solutions offered by the company. You will oversee the implementation and improvement of products like Cliniedge and Clinilearn in clinical settings, ensuring they adhere to the highest standards of clinical excellence, regulatory compliance, and customer satisfaction. Your role will involve leading the clinical strategy and operations for Clinitech India's products, providing clinical expertise to ensure alignment with industry standards, and acting as the clinical liaison between customers, product teams, and internal departments. Additionally, you will oversee the development of Cliniedge, collaborate with the Clinilearn team for continuous improvement, and drive custom publishing of books in coordination with the publishing team. You will work closely with customers to understand their clinical needs and ensure the products meet their specific requirements. Furthermore, you will be responsible for ensuring that Clinitech's products comply with all relevant healthcare regulatory standards and stay updated on evolving healthcare policies to ensure compliance. Monitoring the clinical effectiveness of Cliniedge and Clinilearn, implementing quality improvement initiatives, and driving clinical excellence in product delivery will also be part of your responsibilities. The ideal candidate for this role should have a clinical background, understanding of healthcare technology, and the ability to lead cross-functional teams to deliver top-notch services to clients. A minimum of 5 years of experience in Medico Marketing in Pharmaceuticals/Healthcare organization, along with additional clinical experience, will be beneficial. Strong problem-solving skills, excellent communication, stakeholder management abilities, and organizational skills are essential for this position. Joining Clinitech India will offer you the opportunity to be part of an innovative environment driving clinical transformation with cutting-edge healthcare technologies. You will have the chance to lead clinical operations at a strategic level, influencing healthcare across the country and directly impacting healthcare providers to enhance patient care quality and clinician knowledge nationwide. To apply for this role, please send your resume and cover letter to rajesh.singh@clinitechindia.com.,

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4.0 - 8.0 years

3 - 5 Lacs

Patna, Jaipur, Delhi / NCR

Work from Office

Clinical/ KOL engagement - Various engagement activities including scientific discussions, RTMs, Meetings with KOLs, technical approval for new or existing brands Therapy Awareness and Adoption through conducting CNEs, workshops, nursing awareness. Required Candidate profile must be open to traveling in assigned state. Experience in Infection control / Nursing Training / Nurse educator role in Medical Disposables Organization/ Hospital in Critical Care/ Vascular Access

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7.0 - 11.0 years

0 Lacs

karnataka

On-site

As the Manager, Clinical Operations at Kenvue, you will be responsible for coordinating the operational aspects of Higher complexity clinical studies for Consumer Health products in India, APAC, or EMEA. Your role will involve collaborating with key stakeholders within the Clinical Operations global organization, local India leadership, Study directors, Clinical IT, and Bioresearch Quality & compliance (BRQC). Your primary responsibilities will include leading operational aspects of clinical studies, ensuring compliance with ICH GCP guidelines, company SOPs, and local regulations. You will serve as the point of contact for local projects funded by India R&D, participate in pipeline planning, and mentor junior team members globally. Additionally, you will oversee the selection and evaluation of external service providers, train site personnel, identify quality risks, and develop corrective action plans as needed. Furthermore, you will be responsible for preparing or reviewing essential study documents, overseeing the preparation and release of investigational products, ensuring sponsor oversight, reporting adverse events, maintaining the Trial Master File, coordinating clinical trial disclosures, and writing/reviewing Clinical Study Reports. Your role will also involve providing administrative and technical support to junior Study Managers and aiding in site activation activities. To be successful in this role, you should possess a Bachelor's Degree in a scientific discipline or health care, with a minimum of 7 years of prior clinical study management experience, including at least 2 years in a people/team management capacity. You should have in-depth knowledge of global clinical research regulatory requirements, electronic trial master file management, and clinical trial management systems. Strong leadership, communication, organizational, and problem-solving skills are essential, along with proficiency in Microsoft Word, Excel, and PowerPoint. In return, Kenvue offers a competitive Total Rewards Package*, including paid company holidays, vacation, learning & development opportunities, and employee resource groups. The specific salary range and benefits will be discussed during the recruitment & hiring process. Join us at Kenvue in shaping the future and impacting the lives of millions of people every day through your work as a Manager, Clinical Operations in Bangalore, India.,

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5.0 - 9.0 years

0 Lacs

noida, uttar pradesh

On-site

You will be joining Vital Clinic as a Consultant Dermatologist, with the opportunity to advance to the role of Chief Dermatologist. In this position, you will be responsible for managing clinical operations, overseeing patient care, and contributing to the clinic's growth through patient engagement, marketing, and content creation. The clinic caters to patients seeking aesthetic procedures, non-surgical, and small surgical cosmetic treatments, with a focus on expanding its services. Your primary responsibilities will include providing dermatological consultations and treatments, engaging and converting new patients, managing clinic operations to ensure high standards of care, collaborating on marketing strategies to increase footfall, creating educational content for digital platforms, and eventually taking on a leadership role as the clinic expands. To excel in this role, you should hold an MBBS with MD/DNB in Dermatology or equivalent, have experience in aesthetic dermatology, possess strong leadership and communication skills, and demonstrate a keen interest in marketing and content creation. Your ability to blend clinical expertise with strategic marketing and operational leadership will be crucial for success in this position. This is a full-time, permanent position at Vital Clinic, which has a joint venture with Ratti Brands Private Limited. The role offers the potential for growth into the Chief Dermatologist position based on performance. As a key member of the clinic, you will play a vital role in its success and contribute to its growth and reputation in the field of Aesthetic Dermatological Medicine.,

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15.0 - 24.0 years

15 - 30 Lacs

Chennai

Work from Office

Please reach out to consultwithjanani@gmail.com with your resume or DM your resume to 8825735142. Monitor the functioning of entire business operations, sale in outlets, Doctor’s critical queries on a daily basis & shall report to Functional Head. Required Candidate profile Recent 5 Years of experience with Hospital Pharmacy Background. Age: 30 to 40 Years Willing to Travel, Preferably Male Languages Known: Hindi Must, Fluent English & Local Language (Tamil or Telugu)

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12.0 - 15.0 years

7 - 11 Lacs

Kolkata, Mumbai, New Delhi

Work from Office

As a (Manager, Clinical Operations) you will be joining the worlds largest & most comprehensive clinical research organisation, powered by healthcare intelligence, What You Will Be Doing The responsibilities of the Operations Manager include, but are not limited to: Complete ICON induction and orientation for newly employed employees, Ensure client-specific induction and orientation is planned, communicated and completed, Monitor performance and conduct annual appraisal for each employees, as applicable, Ensure timely identification and resolution of critical issues Client Relationship Managements, Agree Key Performance Indicators with client and periodically review results, You Are Bachelors Degree or local equivalent, in life sciences, medicine or related discipline, Minimum of 12 years of relevant industry experience, Previous experience in clinical project management or/and line management is helpful, Proven ability to identify, analyze and tackle problems, Excellent interpersonal, organizational and management skills, Excellent verbal and written communication skills in English and local language, Strong computer skills, Ability to operate in a multi-cultural environment, Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your familys needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your familys well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

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3.0 - 6.0 years

12 - 18 Lacs

Ranchi

Work from Office

Strong clinical acumen and OT experience Ability to handle emergency surgeries Team player with excellent communication skills Commitment to patient-centric care : MBBS + MS (General Surgery) or equivalent DNB 8169631633

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8.0 - 12.0 years

0 Lacs

varanasi, uttar pradesh

On-site

You are a highly motivated and experienced VP of Hospital Operations responsible for taking complete ownership of hospital functioning and driving operational excellence across various departments. Your key responsibilities include overseeing end-to-end operations of the hospital, such as OPD, IPD, pharmacy, reception, diagnostics, nursing, procurement, maintenance, housekeeping, HR, and finance coordination. You will ensure smooth day-to-day clinical and non-clinical operations, focusing on delivering exceptional patient experiences. In this role, you will lead and supervise departmental heads to ensure compliance with standard operating procedures (SOPs) and proper documentation. Collaboration with medical teams to streamline processes and ensure efficient treatment delivery is essential. You will also be responsible for planning and implementing cost-effective resource management, inventory control, and budgeting. Regulatory compliance, including adherence to NABH, Clinical Establishment Act, and safety norms, will be under your ownership. Monitoring performance metrics and driving improvements in quality, patient outcomes, and service delivery are crucial aspects of your responsibilities. Additionally, you will represent hospital leadership in cross-functional meetings and strategic partnerships. This is a full-time position that requires in-person work at the designated location. For further details or to discuss this opportunity, please contact the employer at +91 9372976783.,

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4.0 - 6.0 years

7 - 9 Lacs

Hyderabad, Bengaluru

Hybrid

Job Title : Pharmacovigilance Specialist Location : Bangalore / Hyderabad Experience : Minimum 4 Years in PV ICSR Job Summary We are seeking a skilled and detail-oriented Pharmacovigilance (PV) Specialist with hands-on experience in Individual Case Safety Reports (ICSR) . The ideal candidate will be responsible for end-to-end case processing and ensuring compliance with global PV regulations and internal SOPs. Key Responsibilities : Perform case intake, triage, data entry, quality review, and submission of ICSRs. Evaluate and code adverse event reports using MedDRA and WHO-DD coding. Ensure timely reporting of adverse events to regulatory authorities and clients. Maintain compliance with pharmacovigilance regulations (e.g., FDA, EMA, CDSCO). Collaborate with cross-functional teams to ensure accurate and complete safety data. Contribute to audit and inspection readiness. Prepare periodic safety update reports (PSURs) and other regulatory documents when required. Qualifications : Bachelors or Masters degree in Pharmacy, Life Sciences, or related field. Minimum 4 years of hands-on experience in PV ICSR processing. Strong understanding of global PV regulations and ICH-GCP guidelines. Familiarity with PV databases (e.g., Argus, ArisG) is an advantage. Excellent attention to detail and strong analytical skills. Good communication and documentation skills. Preferred Attributes : Certification in Pharmacovigilance will be an added advantage. Ability to work independently and as part of a team. Willingness to work in shifts if required (based on client/region).

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2.0 - 4.0 years

4 - 5 Lacs

Hyderabad, Bengaluru

Hybrid

Job Title : Pharmacovigilance Specialist Location : Bangalore / Hyderabad Experience : Minimum 2 Years in PV ICSR Job Summary We are seeking a skilled and detail-oriented Pharmacovigilance (PV) Specialist with hands-on experience in Individual Case Safety Reports (ICSR) . The ideal candidate will be responsible for end-to-end case processing and ensuring compliance with global PV regulations and internal SOPs. Key Responsibilities : Perform case intake, triage, data entry, quality review, and submission of ICSRs. Evaluate and code adverse event reports using MedDRA and WHO-DD coding. Ensure timely reporting of adverse events to regulatory authorities and clients. Maintain compliance with pharmacovigilance regulations (e.g., FDA, EMA, CDSCO). Collaborate with cross-functional teams to ensure accurate and complete safety data. Contribute to audit and inspection readiness. Prepare periodic safety update reports (PSURs) and other regulatory documents when required. Qualifications : Bachelors or Masters degree in Pharmacy, Life Sciences, or related field. Minimum 2 years of hands-on experience in PV ICSR processing. Strong understanding of global PV regulations and ICH-GCP guidelines. Familiarity with PV databases (e.g., Argus, ArisG) is an advantage. Excellent attention to detail and strong analytical skills. Good communication and documentation skills. Preferred Attributes : Certification in Pharmacovigilance will be an added advantage. Ability to work independently and as part of a team. Willingness to work in shifts if required (based on client/region).

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1.0 - 5.0 years

0 - 0 Lacs

Kolkata

Work from Office

Monitor the protocol /compliance for all medical services in the unit. Set up & ensure the regular functioning of the following clinical committees, in consultation with the supervisor - Hospital Infection Control Committee, Academic Council, Monthly Medical Forum, Pharmacy and therapeutic Council and Quality Management Services. Facilitate clinical audit. Coordinate with Infection Control Department to ensure efficient functioning. Ensure adequate coverage through rostering of junior doctors and technicians. Track and maintain medical equipment maintenance requirement and utilization. Manage interdepartmental communication, resolve disputes and / or operational working issues. Ensure proper upkeep& confidentiality of medical records & patient documentation. Work closely with the nursing superintendent and take all necessary steps to ensure high standards of patient care. Ensure that proper procedures are in place for the efficient admission, care & discharge of patients. Coordinate with the Emergency team for all medico-legal cases received at the hospital. Assess and Ensure performance level of staff People-assessment, efficiency etc. Promote continuing professional education of medical, nursing & paramedical staff Management reserves the right to revise JD at any point of time.

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8.0 - 12.0 years

10 - 18 Lacs

Bhiwandi

Hybrid

Role & responsibilities Accountable for: Responsible for clinical trial supply project delivery and quality for strong financial performance & customer satisfaction, in accordance with Clinical Reach's Guidelines, SOPs and practices. Act as mentor to colleagues in regional and local teams Lead or support process improvement initiatives driven by Global Project Management Department DUTIES AND RESPONSIBILITIES: 1. Project Management Operational delivery and reporting of awarded studies. Project delivery is achieved through collaboration with multiple parties including but not limited to client, client's CRO/vendors, sponsor, ZP depots, partner depots, Account Managers, Proposals, Contracts, Clinical Sourcing, Global Operations, Finance, Legal and Compliance colleagues. 2. Contract Management, Budget Control and Monthly Billing Manage project contracts (client work orders, partner depot work orders, change orders etc) and project budgets. Ensure accurate and timely invoicing for client and vendor billings. Participate in the monthly billing process for all projects 3. Client Management Account management of own projects or oversight of projects on assigned client accounts (if any) 4. DPI (Depot Project Instructions documents) Review of DPIs written by other Project Managers (global/ regional/ local) 5. Guidelines/SOPs Adhere to applicable company Guidelines and SOPs. Maintain good knowledge of Good Manufacturing Practice (GMP), Good Storage Distribution Practice (GSDP), Good Documentation Practice (GDP), Data Integrity Policy, Good Clinical Practice (GCP) concepts and Data Integrity Policy. 6. Development of the Global PM Department and Continuous Process Improvement Lead multiple projects independently Lead and contribute to Process Improvement Initiatives Train, mentor and provide supervision to new/junior staff including training, development and input for performance review. Preferred candidate profile SPECIFICATIONS: 1. Required educational level Minimum degree holder with Science or equivalent qualifications, knowledge in Clinical Trial Supply chain management. Preferably with PMI PMP or equivalent certification or working towards one. 2. Required working experience Preferably with 5-10 years of experience of managing regional projects or projects across a few countries Fluent in English 3. Required knowledge & skills. Good inter-personal and communication skills. Good collaboration skills, able to work in a matrix organization. Has customer focus mindset. High execution and decision-making skills, including prioritization skills. Self-motivated and resourceful. Ability to innovate. Good coaching, mentoring and supervisory skills . Perks and benefits

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0.0 - 1.0 years

2 - 5 Lacs

Hyderabad/Secunderabad, Pune, Bengaluru

Work from Office

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

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0.0 - 1.0 years

2 - 5 Lacs

Hyderabad/Secunderabad, Pune, Bengaluru

Work from Office

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

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0.0 - 1.0 years

2 - 3 Lacs

Visakhapatnam, Guntur, Warangal

Work from Office

Manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. Conducts research to ensure these products are safe. Ordering, tracking, and managing IP and trial materials. Required Candidate profile Knowledge of the pharmaceutical industry, terminology, and practices. - Knowledge of FDA regulations and their practical implementation. - Strong verbal and written communication skills.

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1.0 - 2.0 years

3 - 4 Lacs

Hyderabad, Pune, Bengaluru

Work from Office

We are currently hiring for DSA I role with a minimum of 1 year experience in Pharmacovigilance Perform triage & intake of ICSR received daily in ARGUS databases. Ensure data entry of ICSR in ARGUS Required Candidate profile A minimum of 1 year pharmacovigilance case processing experience. Responsible for coding events using MEDDRA Any Life Sciences(B pharm/M Pharm/ Pharm D, Life Sciences, Nursing, BDS, BPT) are Eligible

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0.0 - 1.0 years

2 - 5 Lacs

Hyderabad/Secunderabad, Pune, Bengaluru

Work from Office

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

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0.0 - 1.0 years

3 - 4 Lacs

Hyderabad, Pune, Bengaluru

Work from Office

Medical Writer / Technical Content Writer - Internship This internship is ideal for someone passionate about simplifying medical or technical information into clear, structured documents and engaging content. Good Knowledge of Medical terminology. Required Candidate profile Preparation of protocol for Clinical trials Preparation writing CSR (Clinical Study Report) BDS and MBBS With medical writing for clinical trials Knowledge are Applicable

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0.0 - 1.0 years

2 - 5 Lacs

Hyderabad/Secunderabad, Pune, Bengaluru

Work from Office

Job description Should have knowledge in clinical research studies Perform Site visits (i.e. Site Selection Visit, Site Initiation Visits, Site monitoring visits and site close-out visits) should have knowledge in ICH GCP Guidelines Required Candidate profile Minimum Bachelor's or Masters degree in related field, such as Biology, Chemistry, Nursing, Pharmacy, or Public Health and/or Post-graduate Diploma in Clinical Research Are Applicable to Apply

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8.0 - 13.0 years

8 - 12 Lacs

Halol

Work from Office

Key Responsibilities Design, plan, and oversee clinical trials from initiation to closeout Develop study protocols, informed consent forms, and case report forms Ensure compliance with GCP, ICH, and local regulatory guidelines Manage trial budgets, timelines, and resources Coordinate with CROs, investigators, and ethics committees Monitor trial progress and resolve operational issues Review and analyze clinical data for accuracy and integrity Prepare reports and presentations for internal and external stakeholders Train and mentor clinical research staff Support regulatory submissions and audits Qualifications & Skills M.Pharm / M.Sc / MBBS / MD in Life Sciences, Pharmacy, or Medicine 8-12 years of experience in clinical research, with at least 3 years in a managerial role Strong knowledge of clinical trial design, GCP, and regulatory frameworks

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1.0 - 5.0 years

0 Lacs

karnataka

On-site

As a candidate for the position, you should hold a degree in MHA/MBA-Hospital Administration with a minimum of 1-2 years of relevant experience. In this role, you will be responsible for overseeing the operations and general administration of a well-known rehabilitation center. Your duties will include leading non-medical services, finance, marketing, procurement, and staff, in addition to other tasks assigned by the company. Your key responsibilities will involve ensuring patient care, managing clinical operations, handling financial matters, ensuring compliance, managing personnel, and serving as the interface between patients and the company, as well as staff and the company. You will be tasked with planning and managing appointments and scheduling, collaborating closely with the Marketing team to guarantee effective promotions, lead generations, digital presence, and outreach activities. Moreover, you will be expected to oversee the front office and maintenance team, generate monthly reports as necessary for management, support the company's business objectives and plans, and identify doctors for onboarding while allocating resources to departments. Your role will require hands-on experience in operational management, revenue goal balancing, and operational goal achievement. Your ability to quickly adapt to changes in the business and work environment will be crucial, alongside possessing strong conceptual abilities, communication skills, networking skills, and presentation skills. The job type is full-time and permanent, offering benefits like Provident Fund. The work schedule will be during the day shift. It is essential that you are able to reliably commute or plan to relocate to Bengaluru, Karnataka, before starting work. The education requirement is a Bachelor's degree (Preferred), with a total of 2 years of work experience (Required), including 2 years in an administrative role (Preferred). Proficiency in English, Hindi, Kannada, Telugu, and Tamil is required for this position.,

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8.0 - 12.0 years

0 Lacs

karnataka

On-site

QuartzBio is the Precision Medicine Intelligence Company that specializes in the development of Precision Medicine AI Agent Platform. The platform facilitates autonomous data ingestion and conversational insights throughout the precision medicine value chain. By leveraging a network of domain-specific AI agents, QuartzBio's solutions enhance the efforts of various teams such as operations, translational, informatics, and IT. The integration of biomarker, sample, and clinical data through AI-driven processes creates a unified and scalable data ecosystem. This transformative technology enables R&D teams to expedite the journey from data collection to insights, analytics, and visualizations, ultimately accelerating study completion and time-to-market, thereby revolutionizing the approach of precision medicine teams with 360 intelligence. As a Business Analyst Manager (Business Intelligence) at QuartzBio, you will play a pivotal role in guiding strategic decision-making through advanced business intelligence, data analysis, and cross-functional collaboration. This position necessitates a seasoned analyst capable of collaborating across teams to identify key opportunities in Business intelligence product scope. You will be responsible for conducting analyses and detailing solutions to drive the development of scalable Business intelligence solutions focusing on sample life cycle management and Biomarker data analysis. Key Responsibilities: - Product Strategy & Feature Management: Manage the intake and prioritization of business intelligence product requests, decompose product requirements into features, and collaborate with product leads to define release scopes and develop roadmaps. - Technical Analysis & Integration: Conduct backend data pipeline analysis, translate complex problems into structured analyses, and work closely with AI and intelligent agent teams to integrate BI capabilities. - Cross-Functional Collaboration: Lead product grooming sessions, collaborate with the design team, and partner with engineering teams during sprint demos. - Adoption, Enablement & Innovation: Drive adoption of business intelligence and semantic layers, own the full project lifecycle, and identify opportunities to leverage generative AI. - Continuous Improvement: Stay updated with BI and analytics trends, enhance technical skills, and remain informed about emerging technologies in the BI space. Qualifications: - Bachelor's degree in a related field with a minimum of 8 years of relevant work experience in Business and technical analysis tasks related to Business intelligence. - Proficiency in SQL/MySQL, data visualization tools, and data modeling concepts. - Familiarity with GenAI tools and frameworks is a plus. - Experience with modern data stacks and clinical operations preferred. - Strong problem-solving, analytical, and communication skills. - Proficient in Agile methodologies and project management tools. - Demonstrated leadership in managing complex projects and leading cross-functional initiatives. Leadership Expectations: - Adherence to the company's principles and code of ethics. - Appreciation for individual talents and differences within the team. - Effective communication and support for change initiatives. - Continuous contribution to the development of departmental strategies. Please note that any data provided during the application process will be handled in accordance with our Privacy Policy. If you require a reasonable accommodation or alternative method for applying due to a disability, please contact us. We are committed to ensuring a fair and transparent recruitment process and caution against fraudulent job offers associated with our company.,

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8.0 - 13.0 years

15 - 30 Lacs

Kanpur

Work from Office

Regency Hospital Ltd. Is Hiring! Post:- Medical Superintendent Location:- Kanpur Preferred candidate profile MBBS + MHA/MBA with minimum 5+ Years of experience in Hospital Administration. Role & responsibilities Act as Custodian for Clinical protocols at unit level and ensure high standards of patient care Define and implement Performance Parameters for Doctors. To establish and ensure implementation of NABH guidelines within the unit. Responsible for implementation and adherence to SOPs in all Clinical Specialties, conducting regular Medical Audits on an ongoing basis. Ensure that proper Standard Operative Procedures are in place for the efficient admission, care & discharge of patients Coordination of the patient discharge process between doctors, transcriptionists, nursing, billing and pharmacy. Resident Doctors in general pool and their deployment. Ensure proper upkeep & confidentiality of medical records & patient documentation Develop & implement regular Patient Feedback mechanism Monitor and guide functioning of Dietetics department to ensure service quality. Work closely with the Nursing Superintendent and take all necessary steps to ensure high standards of patient care. Responsible for functioning and maintenance of all Medical Equipments of the hospital including to adhering to SOPs on the uptime of all Medical Equipment. To process and respond to patient feedback. If interested kindly call us at +91 6390015150 or Mail at recruitment.doctors@regencyhealthcare.in Rishabh Singh Gaharwar Corporate HR Regency Hospital Ltd.

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5.0 - 8.0 years

6 - 8 Lacs

Ranchi

Work from Office

JD:- Lead and manage hospital operations across departments Implement SOPs and ensure NABH/compliance readiness Coordinate with clinical and non-clinical teams for service delivery Vendor and facility management

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