365 Clinical Operations Jobs - Page 2

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.

Hiring for Medical Superintendent for reputed Hospital in Noida Qualification :- MBBS is mandatory Interested applicants can directly drop their cv to 9650984828 (Ms. Sana) or at dcss.hrd@gmail.com

Role & responsibilities : Responsible for overseeing hospital administration, clinical services regulatory compliance and quality standards in a teaching hospital and Coordinates with faculty ensures NMC NABH compliance and manages patient care and hospital operations efficiently . 1. Medical Administration & Leadership Oversee the daily operations of all clinical departments. Supervise and coordinate the activities of medical, nursing, and allied health professionals. Ensure proper staffing, discipline, and performance evaluation of medical personnel. Act as the primary liaison between hospital management and medical staff. 2. Quality & Patient Safety Ensure the delivery of high-quality patient care in accordance with medical standards and hospital protocols. Monitor clinical performance indicators and implement continuous quality improvement measures. Lead infection control, patient safety, and clinical audit programs. 3. Regulatory Compliance Ensure the hospital complies with national and local health regulations and accreditation standards (e.g., NABH, JCI). Supervise documentation for medical records, licensing, and compliance inspection Preferred candidate profile : MD/MS in any clinical discipline preferred. Minimum 8 + years of clinical experience with at least 5 years in a leadership or administrative role. Strong leadership, organizational, and communication skills.

BDS + MBA/ MHA Candidate with minimum 6 years of Hospital experience in Medical Administration can share the profiles to shwetha.s@fortishealthcare.com Role & responsibilities To direct, supervise and coordinate functions and activities of one or more departments. To supervise in administration and co-ordinations of medical services. To consult with and advises departmental needs on problems related to operations of the hospitals. To co-ordinate with consultants on issues whenever required. To direct any changes in the functioning of any/all departments. To co-ordinate for accreditation and quality system implementation in the organization. To resolve problems with department HODs concerning to staff and utilization of hospital facilities. To meet with staff members to interpret changes in operational procedures. To assist the Head- Medical services in day to day activities. To communicate information or decisions to the medical staff. To schedule OPD slots and any other medical and Para medical services in association with Head Medical services. To do performance reviews of medical staff in consultation with the Head – Medical services. To sign all the leave applications pass through him/her for approval by Head- Medical services. To co-ordinate with Head - Non-medical services for formal system of allocation of the hospital beds and ensures smooth working of the hospital. To coordinate for committee meetings. To ensure proper inter departmental co-ordination between all the departments of the hospitals. To organize CME programmed/training programs for doctors. To handle customer grievances.

What we want to accomplish and why we need you Suki is a leading technology company that provides AI voice solutions for healthcare. Its mission is to reimagine the healthcare technology stack, making it invisible and assistive to lift the administrative burden from clinicians. Its flagship product is Suki Assistant, an AI assistant that uses generative AI to automatically create clinical documentation by ambiently listening to patient-clinician conversations. Suki helps clinicians complete notes 72% faster on average, assists with other tasks including coding and answering questions, and generates incremental revenue for organizations, delivering a 9X ROI in year 1. Suki also offers its proprietary AI and speech platform, Suki Platform, to partners who want to create best-in-class ambient and voice experiences for their solutions. Clinicians that use Suki already spend over 70% less time on administrative tasks, and we re striving to do even better. Come and join us! We are a user-driven company and are committed to making sure every pixel of our product is in service of the doctors. We re a team of technologists, clinicians, and industry experts working together to push the limits on technology used in medicine. We re confident enough to move fast and talented enough not to break things. Check out this short video to learn more about our mission and our culture. Job Responsibilities What will you do everydayThe Clinical Operations team will collaborate with our clinical and product teams-helping refine the existing product and design new features with the clinicians needs in mind. Translate clinical language into AI logic: Collaborate with AI Engineers to translate your clinical expertise and workflow insights into actionable algorithms for the digital assistant. Create and edit gold standard medical documentation for model training purposes. Continuously refine and optimize: Analyze AI output to evaluate for quality and accuracy from a clinical perspective. Who You Are: Possess a Bachelor of Medicine, Bachelor of Surgery (MBBS) degree and a valid medical license to practice in the respective region. At least 1 year of professional experience in the Department of Paediatrics. 2+ years of practice experience as a doctor (Good to have: working knowledge on US healthcare systems) You have a passion for patient care and the potential of technology to improve healthcare quality and experience. You have strong analytical and problem-solving skills, and are able to identify clinical challenges and translate them into potential AI solutions. You have strong writing skills. You are adaptable and comfortable working in a fast-paced, dynamic environment with evolving technologies. Bonus points: Experience working with digital Health tools or AI Solutions in healthcare. Strong research and analytical skills. Tell me more about Suki Series D raised! On a roll: Announced major partnerships with Google Great team: Founded, managed and backed by successful veterans of Google and Apple in tech and UCSF and Stanford in medicine. We have technologists and doctors working side by side to solve difficult problems. Great investors: We re backed by Venrock, First Round Capital, Flare Capital, March Capital, Hedosophia and others. With our $165M raised so far, we have the resources to scale. Huge market: Disrupting a massive, growing $30+ billion market for transcription, dictation and order entry solutions - our vision is to become the voice user interface for healthcare, bringing innovation that relieves the administrative burden on doctors instead of adding to it. Great customers: Help our doctors save time in their day so they can focus on providing great care. Impact: A fun and exciting start-up culture that empowers its people to make a huge impact. Suki is an Equal Opportunity Employer. We are dedicated to building a company that fosters inclusion and belonging and reflects the diverse communities we serve across the country. We know we are stronger this way and we look forward to growing our team with these shared values.

What we want to accomplish and why we need you Suki is a leading technology company that provides AI voice solutions for healthcare. Its mission is to reimagine the healthcare technology stack, making it invisible and assistive to lift the administrative burden from clinicians. Its flagship product is Suki Assistant, an AI assistant that uses generative AI to automatically create clinical documentation by ambiently listening to patient-clinician conversations. Suki helps clinicians complete notes 72% faster on average, assists with other tasks including coding and answering questions, and generates incremental revenue for organizations, delivering a 9X ROI in year 1. Suki also offers its proprietary AI and speech platform, Suki Platform, to partners who want to create best-in-class ambient and voice experiences for their solutions. Clinicians that use Suki already spend over 70% less time on administrative tasks, and we re striving to do even better. Come and join us! We are a user-driven company and are committed to making sure every pixel of our product is in service of the doctors. We re a team of technologists, clinicians, and industry experts working together to push the limits on technology used in medicine. We re confident enough to move fast and talented enough not to break things. Check out this short video to learn more about our mission and our culture. Job Responsibilities What will you do everydayThe Clinical Operations team will collaborate with our clinical and product teams-helping refine the existing product and design new features with the clinicians needs in mind. Translate clinical language into AI logic: Collaborate with AI Engineers to translate your clinical expertise and workflow insights into actionable algorithms for the digital assistant. Create and edit gold standard medical documentation for model training purposes. Continuously refine and optimize: Analyze AI output to evaluate for quality and accuracy from a clinical perspective. Who You Are: Possess a Bachelor of Medicine, Bachelor of Surgery (MBBS) degree and a valid medical license to practice in the respective region. Minimum of one year s professional experience as a medical coder. 2+ years of practice experience as a doctor (Good to have: working knowledge on US healthcare systems) You have a passion for patient care and the potential of technology to improve healthcare quality and experience. You have strong analytical and problem-solving skills, and are able to identify clinical challenges and translate them into potential AI solutions. You have strong writing skills. You are adaptable and comfortable working in a fast-paced, dynamic environment with evolving technologies. Bonus points: Experience working with digital Health tools or AI Solutions in healthcare. Strong research and analytical skills. Tell me more about Suki Series D raised! On a roll: Announced major partnerships with Google Great team: Founded, managed and backed by successful veterans of Google and Apple in tech and UCSF and Stanford in medicine. We have technologists and doctors working side by side to solve difficult problems. Great investors: We re backed by Venrock, First Round Capital, Flare Capital, March Capital, Hedosophia and others. With our $165M raised so far, we have the resources to scale. Huge market: Disrupting a massive, growing $30+ billion market for transcription, dictation and order entry solutions - our vision is to become the voice user interface for healthcare, bringing innovation that relieves the administrative burden on doctors instead of adding to it. Great customers: Help our doctors save time in their day so they can focus on providing great care. Impact: A fun and exciting start-up culture that empowers its people to make a huge impact. Suki is an Equal Opportunity Employer. We are dedicated to building a company that fosters inclusion and belonging and reflects the diverse communities we serve across the country. We know we are stronger this way and we look forward to growing our team with these shared values.

The Clinical Pharmacist is responsible for ensuring the safe, and cost-efficient use of medications in patient care. Ensure compliance with hospital policies, federal regulations, and accreditation standards NABH.Improvement, and clinical audits.

Responsibilities: * Collaborate with cross-functional teams on study start-up, monitoring & closeout * Manage clinical trials from planning to completion * Ensure compliance with regulatory requirements

To oversee, coordinate, and optimize the day-to-day operations related to patient care services across key functional areas such as OT, Eye OT, CSSD, Cath Lab, Dressing Room, Radiology, OPS, and Pathology. The role also entails supervision and performance monitoring of Patient Care Coordinators, ensuring seamless workflow, service efficiency, and a high standard of patient experience. Key Responsibilities: Ensure efficient functioning and coordination of daily operations in: OT & Eye OT CSSD Cath Lab Dressing Rooms Radiology and Imaging OPD Pathology and Laboratory Units Act as the operational point of contact between clinical departments and administration to resolve process-related issues affecting patient care delivery. Monitor workflow efficiency and address any bottlenecks that affect turnaround time, patient movement, or resource utilization. Ensure patient experience standards are maintained through timely services, courteous communication, and clean, safe environments. Coordinate with nursing, biomedical, housekeeping, and facility teams to ensure readiness and availability of resources and equipment. Ensure compliance with infection control, NABH standards, and other applicable healthcare regulations across managed departments. Generate and present regular reports on department performance, patient flow, issue logs, and service improvement plans. Identify and implement process improvements to enhance efficiency and service quality.

Position – Nursing Coordinator/Field Supervisor Experience – Minimum 2 years of Experience in field operation Travelling and on-boarding Nurses and their assignment management. Coordinate with both patient and Nurses. Personally handle queries. Required Candidate profile Customer Support. Analytical Skill. Good Communication. Staff Management. Geographical Knowledge career@seedsofinnocence.com 8448180806

Job Descriptions : Job Title: Ass. Manager Clinical Research & IPR Job Location: - Plot No. 214, Borsad - Tarapur Road, Ta: Petlad, Dist: Anand, Gujarat, India. Department: R&D / Regulatory Affairs Experience: 7 to 10 years in nutraceuticals, clinical research, and IPR. Industry: Nutraceutical / Food / Pharma Manufacturing Reports To: Head of R&D / Director Job Type: Full-Time Company Profile: - Pharmanza Herbal Pvt. Ltd. is one of the few companies which is focusing on standardizing and proving the efficacy of Herbal products. Our strong supplier base, fully equipped R&D facility, FDA approved manufacturing facility, infrastructure for conducting human trials as well as our formulations unit provides a one stop solution to our valued customers. Pharmanza Herbal Pvt Ltd. is one of the leading research-oriented companies, manufacturing herbal extracts used in the Ayurvedic and nutraceutical segment. Our journey began in 1997 with Pharmanza India, our group company located in Khambhat, India, where we started producing herbal extracts. While Pharmanza India primarily focuses on veterinary allopathic formulations, we leveraged its facilities to manufacture herbal products such as Garcinia cambogia, Commiphora Mukul, and Withania somnifera from 1997 to 2004. As the business expanded, and we began exporting our products to countries like the US, Japan, and Germany. Pharmanza Herbal was established in Dharmaj, India, to continue our commitment to quality and innovation in herbal solutions. The facility is certified by Food safety authority of India (FSSAI), Food and drug Administration, India (Gujarat office) with NSF-GMP International. Current certifications include ISO9001:2015, ISO22000:2018, NSF-GMP, NSF-SPORT,USP-GMP,USP Ashwagandha,Bosewelia with Kosher and Halal and USDA/APEDA organic certifications for products. Additionally, we are also certified SEDEX 4 Pillers and ECOVADIS. Job Overview: - Leads clinical research initiatives, ensures regulatory compliance, manages patent filings, and drives innovation. Collaborates with cross-functional teams to develop strategies, analyze data, and protect intellectual property in alignment with organizational and scientific goals. Responsibilities and Duties: - Clinical Research: Design and execute clinical trials for nutraceutical products (FSSAI-compliant and global standards) Develop study protocols, CRFs, and informed consent documents Coordinate with CROs, ethics committees, and investigators Analyse clinical data for efficacy, safety, and regulatory submissions Prepare Clinical Study Reports (CSRs) and summaries for product dossiers Ensure compliance with ICH-GCP, FSSAI, and international regulatory frameworks Intellectual Property Rights (IPR) Conduct patent landscaping Draft and file patent applications for novel formulations, processes, and delivery systems Monitor competitor IP and identify opportunities for innovation Support trademark filings and brand protection strategies Qualifications: - Education level: - M.Pharm / M.Sc / Ph.D. in Pharmacology, Life Sciences, Biotechnology, or related field and Certification in Clinical Research / IPR (preferred) Gender: - Any. Salary Range: - Competitive. Skills: - Strong understanding of nutraceutical ingredients, formulations, bioavailability enhancement, and clinical endpoints Familiarity with regulatory pathways (FSSAI, DSHEA, EFSA, FDA) Hands-on experience with clinical trial design and statistical analysis Knowledge of patent databases (Espacenet, WIPO, USPTO) and IP strategy Excellent scientific writing and documentation skills Ability to work cross-functionally with R&D, legal, and marketing teams Benefits: Competitive salary package. Subsidized food facility. Free Transportation facility from Vadodara location. Medi-claim facility. Opportunities for professional development and growth. A dynamic and collaborative work environment committed to sustainability. Join our team of passionate professionals and contribute to the growth and success of our nutraceutical product portfolio. If you have the required expertise and are ready to take on this exciting challenge, we encourage you to apply now. Company Website: - www.pharmanzaherbal.com Company Email id: - hrm@pharmanza.com

Job Title: Medical Superintendent (MS) Department: Hospital Operations Location: SPS Hospitals, Ludhiana Position Summary: The Medical Superintendent will be responsible for overseeing and managing all medical and clinical operations at SPS Hospitals. This includes ensuring high standards of patient care, compliance with healthcare regulations, coordination among medical departments, and implementation of clinical governance protocols. The MS acts as a vital link between hospital management and the medical staff, ensuring smooth operations and excellence in patient services. Key Responsibilities: 1. Clinical Governance & Quality Assurance: • Oversee all clinical operations to ensure patient safety and adherence to quality standards. • Implement evidence-based medical practices and ensure compliance with NABH/NABL or other accreditation standards. • Monitor infection control protocols and clinical outcomes. 2. Administrative Leadership: • Coordinate with Heads of Departments (HoDs) for efficient functioning of clinical departments. • Manage medical rosters, staffing levels, duty schedules, and leave planning. • Monitor the implementation of hospital policies related to clinical practice and ethics. 3. Regulatory Compliance: • Ensure all statutory and legal compliances are met, including licensing and documentation. • Liaise with government authorities during inspections and audits. 4. Staff Development & Training: • Facilitate CME (Continuing Medical Education) and training programs for doctors and nursing staff. • Mentor junior clinicians and support ongoing professional development. 5. Patient Services Oversight: • Supervise patient grievance redressal and clinical incident reporting. • Ensure a patient-centered approach in all medical processes and services. 6. Strategic Input: • Support hospital management in strategic planning for clinical services expansion. • Provide inputs on medical technology procurement, department upgrades, and service line development. Qualifications: • MBBS with MD/MS/MHA/MBA or equivalent postgraduate degree in Hospital Administration or Clinical Specialty. • Minimum 10-15 years of clinical experience with at least 5 years in a leadership or administrative role in a tertiary care hospital. • In-depth knowledge of hospital operations, accreditation processes, and healthcare laws. Key Skills: • Leadership & Team Management • Strategic Planning • Clinical Governance • Crisis & Conflict Management • Strong Communication & Interpersonal Skills • Patient-Centric Mindset • Knowledge of Hospital Information Systems (HIS)

Need Licensed Pharmacist (B.Pharm/D.Pharm) for Pandesara, Surat. Duties: dispense meds, promote generics, manage stock & compliance, support customer education. Strong sales & service skills needed. 9AM9PM. 7 Days

At MetLife, we seek to make a meaningful impact in the lives of our customers and our communities. The Global Technology & Operations group (GTO) is a diverse team of engineers, developers, business analysts, claims analysts and project managers with the freedom to create innovative and solutions to address core business challenges with MetLife. This role will work with claimants, physicians, employers, and customers to ensure strict adherence in determining functional abilities. Provides recommendations regarding claimants current/potential functional abilities and develops goal-focused return-to-work plans. To apply, Call HR Parvez at 9810332844 Job Responsibilities Provides professional medical, technical, consulting advice, and recommendations in support of claims evaluation, investigation, and assessment for various claims-related departments, while managing assigned caseload of complex case applying specialized training and knowledge to the assessment of cases and acting as a resource on clinical and technical issues. Conducts complex research, review and analysis of medical records, treatment plans and claim information. Provides recommendations regarding claimants current potential functional abilities and develops goal-focused return-to-work plans. Assess training needs and creates, authors, and presents medical training to claim and business partner associates. Engages claimants, healthcare providers, employers, and customers to ensure strict adherence in determining functional abilities. Engages claimants, health care providers and employers in return to work potential and planning while coaching claim specialists on identifying and acting upon return-to-work potential. Creates effective requests for medical information which focus on clarifying medical restrictions and limitations and their impact on work functionality. Performs other related duties as assigned or required Education, Technical Skills & Other Critical Requirement Bachelors degree (Medical) or diploma with a minimum of 15 years of education. Experience Current RN licensure 4+ years of experience as an RN with Clinical/Ops Experience Preferred 7+ years Disability claims and/or clinical experience. Disability claims experience Preferred designations CCM (certified case management) and/or CDMS (certified disability management specialist).

We are seeking a highly organized and detail-oriented Clinical Trial Coordinator (Fresher) to join our dynamic clinical research team. In this role, you will play a crucial part in ensuring the successful execution of our clinical trials from start to finish. You will collaborate with a multidisciplinary team of researchers, investigators, and study personnel to coordinate all aspects of clinical trial operations. Key Responsibilities: Study Coordination: Coordinate the day-to-day activities of assigned clinical trials, ensuring adherence to protocols, timelines, and regulatory requirements. Site Management: Assist in site selection, initiation, monitoring, and close-out activities. Documentation: Maintain accurate and complete study records, including case report forms, source documents, and regulatory binders. Communication: Facilitate effective communication between study sites, sponsors, investigators, and internal team members. Data Management: Ensure timely and accurate data collection, entry, and query resolution. Regulatory Compliance: Ensure compliance with all applicable regulations, guidelines, and standard operating procedures. Patient Recruitment: Support patient recruitment and retention efforts. Training: Provide training and support to study staff on study protocols and procedures. Quality Assurance: Participate in quality control activities and internal audits. Qualifications and Skills: Education: Bachelor's degree in life sciences, nursing, or a related field. Experience: Fresher or recent graduate with a strong interest in clinical research. Knowledge: Basic understanding of clinical research principles and Good Clinical Practice (GCP). Skills: Excellent organizational, communication, and interpersonal skills.

As a Clin Ops Specialist/CTA based in Athens, your role at Syneos Health will involve performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures, and Work Instructions. You will assist Clinical Monitoring staff with site management activities, serving as a Sponsor representative for assigned studies and ensuring compliance with protocol requirements and relevant guidelines by communicating with sites. Additionally, you will create and assist with maintenance of Trial Master File (TMF) and project files, participate in file audits, prepare site manuals and other documents, update clinical tracking information databases, and track incoming and outgoing clinical and regulatory documents. Your responsibilities will also include managing a shared mailbox, processing site requests, coordinating the ordering, packaging, shipping, and tracking of site supplies and materials, assisting with team meetings, preparing accurate meeting minutes and action items, handling receipt, tracking, and disposition of Case Report Forms and Queries, and maintaining awareness in the field of clinical research through necessary training. To excel in this role, you should possess a High School diploma or equivalent, good communication and interpersonal skills, and the ability to embrace new technologies. Some travel, up to 25%, may be required as part of the role. Syneos Health is dedicated to developing its employees through career progression, supportive line management, technical and therapeutic area training, peer recognition, and a comprehensive total rewards program. The company is committed to fostering a Total Self culture where authenticity is valued, and diversity of thoughts, backgrounds, cultures, and perspectives are embraced to create an inclusive work environment. If you are passionate about making a difference in the field of clinical research, and eager to work in a dynamic and innovative environment where your contributions matter, Syneos Health offers a rewarding opportunity to be part of a global organization that is driven to accelerate the delivery of therapies and change lives. Discover more about Syneos Health and the impactful work we do by visiting http://www.syneoshealth.com. Please note that the tasks, duties, and responsibilities outlined in this job description are not exhaustive, and the company reserves the right to assign additional responsibilities at its discretion. Qualifications may vary based on equivalent experience, skills, and education. Moreover, this description does not create an employment contract, and the company is committed to compliance with relevant legislation to ensure equal opportunities for all employees. Additionally, reasonable accommodations will be provided as per the Americans with Disabilities Act to assist employees or applicants in performing essential job functions.,

Working with Us Challenging. Meaningful. Life-changing. Those aren&apost words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You&aposll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us . Senior Manager, Clinical Scientist Job Title Senior Manager, Clinical Scientist Division R&D / Global Drug Development Functional Area Description The Clinical Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective Will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with the conduct May serve as Clinical Trial Lead for one or more trials May lead or support trial level activities for one or more trials with the necessary supervision May co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members Position Responsibilities Collaborate and liaise with external partners (e.g., KOLs) Seek out and enact best practices with instruction Provide regular and timely updates to manager/management as requested Develop Protocol and ICF documents / amendments and present these to governance committee and development team meetings as required Conduct literature review Submit clinical documents to TMF Develop site and CRA training materials and present these at SIVs and Investigator meetings Review clinical narratives Monitor clinical data for specific trends Develop Data Review Plan in collaboration with Data Management Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming Submit clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, PSUR, Orphan Annual Reports, HA, EC, IRB responses and contribute to regulatory submission.) Degree Requirements Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred). MD-Pharmacology preferred Experience Requirements Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations Ability to understand assigned protocol(s) and their requirements Basic knowledge skills to support program-specific data review and trend identification Intermediate medical writing skills and medical terminology Basic planning/project management skills (develop short range plans that are realistic and effective) Key Competency Requirements Detail-oriented with commitment to quality Basic knowledge of disease area, compound, current clinical landscape Basic knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees Intermediate critical thinking and problem-solving skills Adaptable / flexible (willing and able to adjust to multiple demands and shifting priorities; ability to meet day-to-day challenges with confidence and professionalism) Intermediate skills in Microsoft Word/Excel/PowerPoint and data review tools (e.g., Pt Profiles, report generating tools) Travel Required Domestic and International travel may be required. If you come across a role that intrigues you but doesn&apost perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [HIDDEN TEXT] . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https //careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. 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Location: Bangalore (Hybrid) Working Days: 6 days/week Elevate Now is looking for a Clinical Operations Associate Director to lead and scale our clinical operations. This role is ideal for someone with a strong foundation in medicine, deep knowledge of weight loss, nutrition, and supplements , and a genuine passion for improving patient health outcomes. You will be responsible for managing doctors, ensuring high-quality clinical practices, and driving operational excellence in a fast-paced startup environment. Interested candidates can share their resume and details to [HIDDEN TEXT] Key Responsibilities Oversee end-to-end clinical operations , ensuring compliance with medical standards and protocols. Manage, mentor, and engage with the doctor network (in-house and consultants). Design and implement clinical workflows, treatment protocols, and patient care journeys for weight loss and supplement programs. Work closely with product, tech, and ops teams to integrate clinical excellence into the platform. Monitor patient outcomes and feedback to improve service quality and consistency. Ensure ethical medical practices, patient safety, and regulatory compliance. Collaborate with external vendors, partners, and stakeholders where required. Designing hiring and training processes for doctors Requirements Medical/Clinical background (MBBS, MD, or related qualification preferred). Strong knowledge of weight management, obesity medicine, nutrition, and supplements . 610 years of experience in clinical operations/doctor management ; startup or digital health experience is a plus. Empathetic, patient-first approach with strong communication and leadership skills. Ability to work in a fast-paced, dynamic startup culture with a hands-on attitude. Based in Bangalore, comfortable with a hybrid working model . What We Offer Opportunity to shape clinical operations from the ground up in a growing health-tech startup. A passionate and mission-driven team. Growth-oriented environment with the chance to build and lead a strong clinical team. Interested candidates can share their resume and details to [HIDDEN TEXT] Show more Show less

Responsible for entire operation of the hospital handling financial / customer / process / people responsibilities Spearhead the development, communication and implementation of effective growth strategies Responsible for providing strategic inputs to the management. Ensure hospital's strategic direction is communicated to concerned stakeholders, directs focused activities and is supported by the Management Team Create quarterly and annual budgets including Capex & Opex Budgeting Drive the revenue generation and cost control for the unit. Assure cost effectiveness and financial integrity, with emphasis on revenue enhancement, productivity, utilization management and overall profitability. Monitor expenses and suggest cost-effective alternatives Provide leadership to the team while creating a positive and productive culture, achieving high morale, quality outcomes and positive financial results. Implement effective policies for all operational procedures. Setting and following standards for operational excellence to maximize the efficiency and effectiveness of human, material and financial resources in the organization Responsible for delivering the best quality of patient care Implement clinical procedures and policies Hire and retain qualified staff; doctor recruitment is a key responsibility Develop a relationship with outside organisations, including the medical community, referring physicians • Given BMB's focus on clinical excellence and advanced procedures, a unit head with a strong clinical background, preferably a clinical doctor would be ideal. • Some experience in a hospital setting is crucial for effectively managing the CAPEX, OPEX, clinical engagement, and complex manpower dynamics (Unionised workforce) involved. • Someone with relevant experience in driving clinician engagement, models of empanelment etc

Uncover Wellness is a leading omnichannel platform offering advanced skin, hair, and body treatments through a blend of in-clinic, at-home, and online services. We specialize in delivering personalized treatments by a team of expert counselors, aestheticians, and dermatologists to address a variety of aesthetic concerns. Job Overview: We are seeking a dynamic and highly organized Clinic Manager to oversee day-to-day operations at our Gurgaon clinic. The Clinic Manager will ensure the smooth functioning of the clinic, focusing on staff management, client satisfaction, operational excellence, and revenue growth. Key Responsibilities: Oversee the daily operations of the clinic, ensuring everything runs smoothly and efficiently for both staff and clients. Drive the clinics revenue by monitoring sales, setting goals, and collaborating on promotions that resonate with clients. Lead and support your team, fostering a positive work environment and ensuring everyone is well-trained and motivated. Build strong relationships with clients, ensuring they have a great experience and feel taken care of from start to finish. Keep everything organized and compliant, from record-keeping to ensuring the clinic operates seamlessly. Continuously look for ways to improve processes, enhance client satisfaction, and grow the clinics reputation in the community. Preferred Qualifications: Experience working in a skin, laser, or wellness clinic environment. Knowledge of sales processes and performance management. Ability to handle multiple tasks efficiently under pressure. Why Join Us: Competitive salary with performance incentives. Opportunities for career growth and professional development. Work in a state-of-the-art facility with a team of dedicated professionals. Be part of a fast-growing and innovative company shaping the future of wellness and aesthetics.

Role & responsibilities We're seeking an experienced Medical Superintendent to lead our medical team and oversee hospital operations. The successful candidate will be responsible for ensuring high-quality patient care, managing hospital resources, and implementing policies to improve medical services. 1. Clinical Leadership: Provide medical leadership and guidance to hospital staff, ensuring high-quality patient care and adherence to medical standards. 2. Hospital Operations: Oversee hospital operations, including patient flow, bed management, and emergency services. 3. Quality Improvement: Develop and implement policies to improve patient safety, quality of care, and patient satisfaction. 4. Staff Management: Manage and supervise medical staff, including recruitment, training, and performance evaluation. 5. Resource Management: Oversee hospital resources, including budgeting, procurement, and inventory management. 6. Compliance: Ensure compliance with regulatory requirements, accreditation standards, and hospital policies. 7. Communication: Foster effective communication among hospital staff, patients, and stakeholders. 8. Strategic Planning: Participate in strategic planning to improve hospital services and achieve organizational goals Preferred candidate profile - MBBS degree with a postgraduate degree in hospital administration or a related field - Proven experience as a Medical Superintendent or similar role - Strong clinical and administrative skills - Excellent leadership and communication skills - Ability to work in a fast-paced environment and make informed decisions What We Offer: - Competitive salary and benefits package - Opportunities for professional growth and development - Collaborative and dynamic work environment

MBBS with MD; JD preferred. Proven experience in hospital clinical operations and leadership required. Strong coordination skills with clinical departments and a focus on quality patient care

We are seeking a skilled and compassionate General Nursing and Midwifery (GNM) Nurse with a minimum of 3 years of experience to become a valuable member of our healthcare team. As a GNM Nurse, you will be responsible for delivering exceptional patient care, collaborating with doctors, and ensuring the seamless operation of clinical activities. The ideal candidate will exhibit a strong commitment to providing high-quality care to patients. In addition, you will have the opportunity to assist physicians in medical procedures and treatments, thereby contributing to the overall well-being of our patients. As a part of our team, you can look forward to a competitive salary along with performance-based incentives. We also offer health insurance and a range of employee benefits to support your overall well-being. Furthermore, there are avenues for professional development and training to help you enhance your skills and knowledge in the healthcare field. Job Types: Full-time, Permanent, Fresher Benefits: - Cell phone reimbursement - Food provided - Provident Fund Schedule: - Day shift - Morning shift In addition to the above benefits, there is a performance bonus scheme in place to recognize and reward your hard work and dedication. Language: - Hindi (Preferred) Work Location: On-site (In person) Join us in our mission to deliver exceptional healthcare services and make a positive impact on the lives of our patients. Apply now and be a part of our dedicated healthcare team.,

Role & responsibilities: Set-up, maintain and/or close out project files and study information ((e.g., regulatory documents, Trial Master File (TMF), enrollment, Adverse Events (AEs)/Serious Adverse Events (SAEs), site supplies, Institutional Review Board re-approvals, data queries) on a variety of databases and systems. Attends, participates, prepares and distributes meeting minutes and action items for both internal and external meetings (sponsor, trusted process, functional, investigator meetings). Follows up with team members on action items to closure. Maintains timely and effective communication among team members and site staff. Keeps Project Leadership and Clinical Research Associates (CRAs) fully apprised of sites and study status. May contact site staff as needed for critical information. Provide administrative support to Project Leads and functional leads. Ensure all study documents are archived based on the appropriate guidelines and policy. Provide support for quality assurance activities, including preparation for audits and internal review, prepare documentation and follow through to resolution on actionable issues.

Role & responsibilities: Set-up, maintain and close out project files and study information ((e.g., KPIs, regulatory documents, Trial Master File (TMF), enrollment, Adverse Events (AEs)/Serious Adverse Events (SAEs), protocol deviations, site supplies, Institutional Review Board re-approvals, data queries) on a variety of databases and systems. Maintain and distribute study-specific /financial reports (e.g. vendor/site invoices, investigator payments (grants and pass-through), forecasts, etc). May lead internal and external meetings as directed by the PL Prepares and distributes meeting minutes and action items for both internal and external meetings (sponsor, trusted process, functional, investigator meetings). Follows up with team members on action items to closure. Records the status of Key Performance Indicators (KPIs) in assigned systems, with input and oversight from the assigned PL. Assesses and communicates KPIs for associated job tasks to PL with proposed action plan. Prepares and provides status reports to customers with oversight from assigned PL Ensure all study documents are archived based on the appropriate guidelines and policy. May serve as project representative for internal and external audits. Provide support for quality assurance activities, including preparation for audits and internal review, preparing documentation and follow through to resolution actionable issues. May serve as primary customer contact when PL is out of the office. Seeks input from Project Director for customer support.