799 Clinical Operations Jobs - Page 12

As a Clinical Operations Manager at Novaspire, your role involves leading the operational planning and execution of Phase I-IV clinical trials across multiple therapeutic areas. You will be responsible for coordinating study start-up activities, managing CROs, vendors, and clinical sites, and ensuring timely delivery of study objectives. Your key responsibilities include: - Coordinating study start-up activities such as site selection, feasibility, contract negotiations, and ethics/regulatory submissions. - Developing and maintaining project timelines, budgets, risk mitigation strategies, and status reports. - Monitoring recruitment, data collection, protocol adherence, and query resolution ...

As a Learning and Development Manager at Almas Hospital, Kottakkal, your role is crucial in enhancing staff training, orientation, and career development programs to ensure continuous professional growth. Your primary responsibilities will include: - Assessing organizational learning needs and designing structured training programs accordingly. - Leading the development, delivery, and evaluation of orientation programs for new joiners, including nurses and clinical staff. - Conducting training sessions on clinical competencies, soft skills, leadership, safety protocols, and policy compliance. - Collaborating with nursing and other department heads to identify specific skill gaps and training...

As a Centralized Clinical Trial Manager at ICON, you will be responsible for leading the centralized monitoring activities for clinical trials to ensure trial quality and patient safety. Your key responsibilities will include: - Leading the centralized monitoring activities for clinical trials, including data review and risk-based monitoring. - Collaborating with clinical operations, data management, and biostatistics teams to identify potential risks and ensure proactive management of trial data. - Ensuring study compliance with regulatory requirements and protocols by overseeing real-time data reviews and monitoring activities. - Providing oversight on site performance, patient safety, and...

Join Novartis as an Associate, Managed Access Programs (MAP) & Post-Study Drug Supply (PSDS) Operations and play a key role in supporting patient access to innovative therapies. You will contribute to the planning and execution of these programs, collaborating with global teams to ensure medicines reach those who need them - efficiently, compliantly, and with high quality. Your commitment to operational excellence and attention to detail will help simplify processes and uphold the highest standards, making a meaningful impact on patients and healthcare. Key Responsibilities: - Support completion of MAP and PSDS strategy plans with input from cross-functional teams. - Assist with operational ...

Roles and Responsibilities Manage day-to-day operations of the hospital, ensuring smooth functioning of all departments. Oversee clinical services, including patient care, medical records, and quality improvement initiatives. Develop and implement policies to improve operational efficiency, reduce costs, and enhance patient satisfaction. Collaborate with healthcare teams to develop strategic plans for growth and development of the hospital. To manage the clinical team effectively for providing quality healthcare services to patients To improve the overall patient flow by improving operation efficiency. To conduct medical camps regularly with the clinical team. Ensure compliance with regulato...

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top manag...

As an experienced Head of Operations at Serturner, you will be responsible for leading and streamlining our procurement and warehouse operations to ensure efficient distribution and dispatch of medicines, equipment, and consumables. Your role will involve overseeing end-to-end supply chain processes, maintaining vendor relationships, optimizing inventory, and ensuring regulatory compliance across all operations. Key Responsibilities: - Lead and manage procurement of medicines, medical equipment, and consumables. - Oversee warehouse operations in Naigaon, including storage, inventory control, and dispatch. - Ensure timely and accurate distribution to partner centers and clients. - Build and m...

Role & responsibilities Job Duties: To supervise and coordinate activities of physiotherapy program designed to treat disabled, injured or diseased patients. To discuss with physicians/surgeons regarding patients treatment in accordance with available treatment modalities. To introduce and demonstrate new techniques of treatment. To observe patients' actions and reactions to prescribed treatment and evaluate progress. To train new personnel ; Take classes for students and nurses to discuss and evaluate patients' condition, progress, and plans for further therapy. To instruct and demonstrate to outpatients exercises to be performed at home. To establish goals and policies for the physiotherap...

Responsibilities: * Collaborate with healthcare team on treatment plans. * Manage emergencies, provide patient care in ICU setting. * Conduct diagnostics, oversee clinical ops & manage ICU patients.

Company Description At Novaspire, we pride ourselves on being a trusted partner to the pharmaceutical industry, dedicated to delivering comprehensive, high-quality clinical research services. We support pharmaceutical, biotechnology, medical device, and nutraceutical companies at every stage of the product development lifecycle, from Phase I clinical studies to post-market surveillance. Our core services include pharmacovigilance, clinical trials, medical writing, bioequivalence study support, GxP consulting services and training, and imaging studies. We are committed to ensuring patient safety, regulatory compliance, and high-quality data to enhance clinical trial outcomes. Role Description...

Oversee the nursing department, ensuring efficient operations and high-quality patient care. Implement hospital policies & rules Staff Management Quality Assurance Patient Care Coordination Policy and Procedure Development Quality Improvement

Assist in planning, initiation, and execution of clinical trials. Conduct site monitoring visits and ensure adherence to study protocols, SOPs, and regulatory requirements. Please call- 7026629008 / 8050011327 for further details.

Responsibilities: * Lead hospital operations & staff development * Oversee clinical services & patient care * Ensure NABH compliance & medical safety * Manage budgets & resource allocation

GCS Medical College, Hospital & Research Centre is looking for Sr. Dialysis Technician to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applyin...

Job Summary We are seeking a highly skilled and proactive Veeva CTMS Subject Matter Expert (SME) to join our consulting firm and support our Life Sciences clients in optimizing clinical trial management processes. This role will be responsible for managing Veeva CTMS, eTMF, EDC implementations, ensuring compliance, and enabling efficient trial lifecycle management for our clients. Key Responsibilities Act as the subject matter expert (SME) for Veeva CTMS, eTMF, and EDC across our Life Sciences consulting projects. Lead end-to-end configuration of Veeva CTMS, eTMF, and EDC to support clinical trial planning, execution, data management, and reporting for various clients. Manage stakeholder rel...

Position Summary: • We are looking out for a Senior Clinical Data Associate who will be working on Beacon Targeted Therapies (https://beacon-intelligence.com); a database from our UK based Client, Hanson Wade. • Beacon is a drugs, clinical trials, deals & companies intelligence database based on modular solutions focusing on various therapeutic areas. • The content is manually curated by researchers providing in-depth data to help identify the most relevant trends in the landscape. You will be part of a global network of life science researchers working on dynamic, fast growing products in exciting, cutting-edge life science areas. Key Accountabilities / Responsibilities: • Lead and manage r...

About the Role Join Novartis as a Senior Associate, Managed Access Programs (MAP) Post-Study Drug Supply (PSDS) Operations and play a vital role in supporting patient access to innovative therapies. You will independently contribute to the planning and execution of these programs, collaborating with global teams to ensure medicines reach those who need them - efficiently, compliantly, and with high quality. Your commitment to operational excellence and attention to detail will help simplify processes and uphold the highest standards, making a meaningful impact on patients and healthcare. Key Responsibilities Support completion of MAP and PSDS strategy plans with input from cross-functional t...

Company Description QREC Clinical Research LLP is a Contract Research Organisation with offices in Jaipur (India), Hyderabad (India), and Dubai (UAE). They offer comprehensive services to the healthcare industry, including clinical trials (Phase 3 & 4), REAL WORLD, observational studies, PMS, KAP surveys, investigator-initiated studies, medical writing, clinical data management, statistical analysis, and medico marketing globally. QREC has contributed significantly to the healthcare industry with over 450 brand plans, 162 REAL world studies, 9 global studies, and numerous other projects. Their extensive database includes 45,000+ doctors, 810,000+ patients, and 180+ publications, and they hav...

As a Business analyst at eClinical Solutions, your role will involve collaborating with various teams to optimize clinical operations workflows, enhance data management efficiency, and ensure seamless adoption of technology solutions aligned with organizational objectives. - Manage end-to-end implementation projects of eClinical Solutions, ensuring adherence to timelines, budgets, and quality standards. - Collaborate with external stakeholders to gather requirements and define project scopes for technology implementation and business process reengineering. - Develop comprehensive project plans, including resource allocation and risk assessment, to drive successful execution. - Coordinate wit...

Responsibilities: Provide expert advice on clinical operations and beauty products within the cosmetics industry. Collaborate with sales team to drive revenue growth. Develop strategic plans for clients' businesses.

Role & responsibilities Ensure compliance with NABH standards through regular audits and inspections. Oversee clinical operations, including emergency preparedness and disaster management plans. Manage hospital administration, coordinating with various departments to ensure smooth functioning. Conduct quality accreditation processes to maintain high-quality patient care. Review medical records and reports to identify areas for improvement. Preferred candidate profile MBBS degree + MBA/PGDM (Any Specialization) or equivalent qualification. Minimum 5-10 years of experience in healthcare services industry. Strong knowledge of clinical coordination, clinical operations, hospital administration, ...

Provide expert support and functional and technical knowledge to ensure the scientific integrity/validity for clinical development, early development, and/or research projects Participate in the full lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities along with providing quantitative analytical support Provide statistical support for regulatory submissions including planning, analysis and reporting of clinical safety and efficacy summaries May also provide statistical support to research or other R&...

Step into a role where innovation meets impact As a Digital Endpoint Expert, youll be a key member of the Digital Endpoint Capability Centre, driving the coordination, implementation, and deployment of digital endpoints and digital health technologies across clinical trials Youll bridge digital health expertise and clinical trial excellence, working closely with trial teams and cross-functional stakeholders to ensure seamless delivery Your leadership will shape the integration of novel measures across the development organization, while your expertise will help define implementation strategies tailored to each indication and trial design If you're passionate about digital health and ready to...

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile and Allergy Therapy Products, and Generics and APIs, comprising Solid Dosage Formulations and Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research and Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another a...

KRA Deliverables / Targets 1. Quality Control - Ensure correctness of all reports with necessary cross-reference from clinical history. - Communicate with concerned doctors/clients in case of highly abnormal reports. Target: 99.5% report correctness to be achieved. 2. Turnaround Time (TAT) - Monitor TAT from sample registration (accession) to report release. Target: 95% compliance at all locations. 3. Grievance Redressal - Address all grievances through re-testing or direct communication with clients/doctors, wherever required. Target: 100% resolution of reported grievances. 4. Equipment Maintenance & Calibration (CPRT) - Maintain AMCs strictly as per requirement. - Use minimum controls/cali...