581 Clinical Operations Jobs - Page 2

Manage and oversee clinical data management activities, ensuring compliance with regulatory requirements. Develop and implement effective data management plans to ensure data quality and integrity. Required Candidate profile Strong knowledge of clinical data management principles and practices. Experience with data management systems and software applications. Excellent analytical and problem-solving skills.

Manage and oversee clinical data management activities, ensuring compliance with regulatory requirements. Develop and implement effective data management plans to ensure data quality and integrity. Collaborate with cross-functional teams Required Candidate profile Strong knowledge of clinical data management principles and practices. Experience with data management systems and software applications. Excellent analytical and problem-solving skills

Manage and oversee clinical data management activities, ensuring compliance with regulatory requirements. Develop and implement effective data management plans to ensure data quality and integrity. Collaborate with cross-functional teams Required Candidate profile Strong knowledge of clinical data management principles and practices. Experience with data management systems and software applications. Excellent analytical and problem-solving skills

Collaborate with cross-functional teams to develop and implement clinical research studies. Provide medical expertise and guidance on study design, methodology, and statistical analysis. Develop and maintain relationships with key stakeholders Required Candidate profile Strong understanding of clinical research principles, methodologies, and regulations. Excellent communication and interpersonal skills, with the ability to work effectively with diverse stakeholders.

Conduct thorough medical reviews and assessments to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to develop and implement clinical development strategies. Provide expert guidance on medical aspects Required Candidate profile Strong understanding of clinical development principles and practices. Excellent analytical and problem-solving skills, with attention to detail. Effective communication and interpersonal skills

Monitor medical enquiries and respond to queries from clients and stakeholders. Provide excellent customer service and ensure timely resolution of medical inquiries. Collaborate with internal teams to resolve complex medical issues. Required Candidate profile Strong knowledge of medical terminology and concepts. Excellent communication and interpersonal skills. Ability to work effectively in a fast-paced environment and prioritize tasks.

Manage and oversee clinical data management activities, ensuring compliance with regulatory requirements. Develop and implement effective data management plans to ensure data quality and integrity. Collaborate with cross-functional teams to identify Required Candidate profile Strong knowledge of clinical data management principles and practices. Experience with data management systems and software applications. Excellent analytical and problem-solving skills

Responsibilities Clinical Leadership: Manage clinic team, including Doctors, Aesthetician nurses, and other ops team members. Provide expert guidance on clinical practices, protocols, and patient care standards. Ensure the standard of care and adherence to medical practices. Quality Assurance & Compliance: Oversee clinical audits, ensuring compliance with necessary regulations and standards. Implement and monitor quality improvement initiatives to enhance patient journey. Ensure compliance with all legal, regulatory, and accreditation requirements related to clinical operations. Policy Development: Develop and implement medical policies, procedures, and protocols in collaboration with senior...

Summary The GCP Compliance Specialist (Technology) is accountable to manage delegated activities supporting GCO projects and teams in ensuring compliance against GCP for emerging technology and change of strategy in current GCO managed technology, including awareness of the use of artificial intelligence (AI) and machine learning in GCO operated clinical trials, with the aim to guarantee regulatory adherence in the use of computerized systems and in the collection of electronic data. The GCP Compliance Specialist (Technology) provides data analytics and reporting support, knowledge in GxP relevant Enterprise IT systems in the frame of GCP Compliance activities and supports the delivery of th...

Job Summary: The Night Shift Operations Manager will be responsible for overseeing and managing all hospital operations during night hours. This includes supervising staff performance, ensuring smooth patient services, maintaining safety and security, handling emergencies, and ensuring compliance with hospital policies and procedures. Key Responsibilities: Operational Supervision Ensure smooth functioning of all hospital departments during the night shift (ICU, IPD, Emergency, Lab, Radiology, Security, Housekeeping, etc.). Monitor patient admissions, discharges, and transfers. Coordinate with doctors, nurses, and support staff to resolve operational issues promptly. Patient Care Coordination...

Roles and Responsibilities Manage day-to-day hospital operations, ensuring smooth functioning of all departments. Oversee clinical operations, including patient care, treatment planning, and staff supervision. Develop and implement operational strategies to improve efficiency, quality of care, and patient satisfaction. Collaborate with medical teams to ensure effective communication and coordination of services. Ensure compliance with regulatory requirements, policies, and procedures.

A Reputed Hospital is looking for Hospital Quality Manager based at Ankleshwar , Gujarat location Key Responsibilities: Implement and monitor compliance with NABH standards.Do periodic Internal Audits for standard Compliance. Coordinate periodic gap assessments and ensure timely closure of non-conformities. Monitor KPIs and assist departments in achieving targets. Do trend Analysis for KPIs, Patient feedback, Active Audits etc.. Prepare and maintain documentation as per accreditation norms. Prepare, review, and manage SOPs, manuals, policies, and quality documentation. Facilitate incident reporting system hospital-wide. Perform root cause analysis and support CAPA (Corrective and Preventive ...

Help us bring cutting-edge medical treatments to life! Become a key player in clinical research and accelerate advancements in healthcare. Opportunities We offer two paths into the exciting world of clinical research: Internship: Get a hands-on introduction to clinical trials through a time-bound internship program. Ideal for students or recent graduates eager to experience the field. Fresher-Level Position: Launch your career as a Clinical Research Coordinator! This position offers ongoing employment for those committed to this exciting field. Regardless of path, you'll get to: Manage the flow of clinical trials: Oversee study logistics, participant documentation, and ensure the study progr...

The Clinical Data Coordinator (Intern/Fresher Level) plays a crucial role in ensuring the integrity and quality of clinical trial data. This position offers a valuable entry point into the field, providing hands-on experience in core data management tasks and industry best practices. Key Responsibilities: Data Entry and Verification: Meticulous data entry into electronic data capture (EDC) systems. Verify data accuracy and consistency against source documents (e.g., Case Report Forms). Learn to identify and flag potential data discrepancies. Query Generation and Resolution: Develop an understanding of data discrepancies and their underlying causes. Assist in generating data queries to clarif...

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. Document...

Role Overview: As a Veeva CTMS Subject Matter Expert (SME) at our consulting firm, your role will involve optimizing clinical trial management processes for our Life Sciences clients. You will be responsible for managing Veeva CTMS, eTMF, and EDC implementations to ensure compliance and enable efficient trial lifecycle management. 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 relationships with clients to gather requiremen...

Senior CDC Bangalore/Chennai/Trivandrum, India Immediate Joiner ICON plc is a world-leading healthcare intelligence and clinical research organization Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development, We are currently seeking a Senior Clinical Data Coordinator to join our diverse and dynamic team As a Clinical Data Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies, What You Will Be Doing Create and maintain detailed data m...

Clinical Trial Associate (Bangalore) ICON plc is a world-leading healthcare intelligence and clinical research organization Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development, We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies, What You Will Be Doing Assist in the coordination and administration...

Roles and Responsibilities Manage day-to-day operations of the Clinic, ensuring smooth functioning of all departments. Coordinate with various stakeholders including doctors, nurses, technicians, and other staff members. Ensure compliance with regulatory requirements and maintain high standards of quality care.

Support the implementation of PSEA awareness activities and encourage completion of mandatory training for relevant groups. Participate in the development, implementation, and enhancement of processes, controls, and tools in collaboration with cross-functional teams. Monitor actionable metrics and KPIs, initiate remediation actions as needed, and escalate concerns to the Medical Operations Manager or local PSEA Committee for recommendation or arbitration. Track compliance metrics for Patient Programs and related initiatives by preparing reports and trend analyses at defined intervals. Coordinate regular review meetings with internal stakeholders for Patient Programs and other related activit...

senior administrative and medical officer responsible for the overall management of a hospital's operations, including financial planning, staff supervision, and ensuring high standards of patient care and regulatory compliance,

Why Join Us Be part of India's fastest-growing pet healthcare brand. High-ownership role with direct impact on a high-potential vertical. Work with a passionate and mission-driven team of vets, groomers, and pet lovers. Career growth across multiple locations and roles. A culture that values transparency, fairness, and customer-first thinking. Effective communication across diverse stakeholders Role & responsibilities Centre Operations & Experience Ensure smooth daily operations across clinic and grooming functions. Own patient flow, wait time, NPS, service delivery, and overall customer experience. Maintain clean, pet-safe, and fear-free environments as per brand guidelines. Monitor real-ti...

Key Responsibilities: 1. Operational Management: Monitor daily functioning of patient care services in dialysis, ICU, general/speciality wards, physiotherapy, oncology, dietetics, and pharmacy. Ensure timely and effective patient services by coordinating with nursing, medical, and paramedical teams. Conduct regular rounds across departments to ensure cleanliness, service delivery, and adherence to protocols. Address patient or family concerns proactively and escalate unresolved issues appropriately. 2. Interdepartmental Coordination: Act as a liaison between departments to resolve interdepartmental issues affecting patient care. Ensure seamless communication between clinical staff and suppor...

Site Name: Bengaluru Luxor North Tower Posted Date: Oct 21 2025 Job Purpose The Associate Director, Team Lead Integrated System Support is responsible for managing a team that supports or owns clinical business systems throughout their lifecycle. This includes ensuring systems owned or supported by the team are compliant, reliable, efficient, and user-friendly. Key Responsibilities For systems assigned to the team lead's team: Reliable, Compliant & Fit-for-Purpose System Landscape: Ensure systems comply with relevant external and internal guidelines, regulations and policies and that adequate documentation is maintained, archived and retrievable that demonstrate that systems are reliable, co...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description About the Role We seek a highly skilled Country Approval Specialist to join our Clinical Operations team in India. This outstanding opportunity lets you lead/exel in clinical operations team and collaboration. As a vital team member, you will ensure flawless execution of study startup phase, meeting all regulatory requirements and industry standards. Responsibilities Determine and prepare country-specific submission dossiers for DCGI & EC meeting regulatory requirements for clinical trial submissions. Successfully implement submission strategies to acquire regulatory and ethics committee approvals. Forecast time...