799 Clinical Operations Jobs - Page 2

Site Services Specialist I - Bangalore, India - Hybrid, Office-based ICON plc is a world-leading healthcare intelligence and clinical research organization. We're 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 Site Services Specialist I to join our diverse and dynamic team. As a Site Services Specialist I at ICON, you will play a key role in supporting clinical trial sites by managing logistics, resolving site-related issues, and ensuring that sites are equipped with the necessary resources to conduct trials effectively. You will contribute to the s...

Job Description : Work Schedule Standard (Mon-Fri) Environmental Conditions Office 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 ti...

Manage and maintain large datasets to support marketing campaigns. Develop and implement data management processes to ensure accuracy and integrity. Collaborate with cross-functional teams to design and execute targeted marketing programs. Analyze data trends and patterns to inform business decisions. Design and develop reports and dashboards to track key performance indicators. Ensure compliance with data security and privacy regulations. Job Requirements Bachelor's degree in Business Administration, Computer Science, or related field. Proven expertise in marketing programs, data management, or systems operations. Strong attention to detail and ability to ensure data accuracy. Demonstrated ...

Roles & Responsibilities: Core Objective: To handle operations of the center seamlessly Drives the center revenue and achieves target Contributes directly to top line revenue Core Skills: Good oral and written communication skills in Regional Language, English Good people skills, be a Team player - Networking & Relationship Building Personal integrity, ability to deal with sensitive issues with tact, diplomacy and judgment Maintain complete discretion and confidentiality Planning, Organizing, Prioritizing & Time Management skills Personal Grooming, Good Etiquette Ability to handle stress, crisis management & extended working hours. Job description Ensure smooth functioning of all healthcare ...

About The Role: The Clinical Document Specialist (CDS) will provide support for Trial Master File (TMF) activities to the clinical teams for assigned projects. This role will be responsible for the overall management and quality maintenance of essential clinical trial and other designated documents, including the set up and maintenance of the Trial Master File (TMF) The CDS will have a strong focus on ensuring routine document management operations are performed with adherence to Novotech SOPs. This role to manage Trial Master Files (TMF), both electronic and paper in format according to project requirements, ICH GCP guidelines, local/global regulatory requirements and Novotech/Client SOPs. ...

Core Responsibilities Own end-to-end delivery for assigned client projects across clinical data management, analytics, data science, and information management. Lead sprint planning, effort estimation, resource allocation, risk/issue management, and status reporting; ensure on-time and on-budget outcomes. Perform hands-on solutioning and execution (e.g., gathering business requirements, writing data pipelines, standards mapping, model building, dashboarding etc.) while guiding junior team members. Collaborate with client stakeholders (ClinOps, Biometrics, Safety, Medical Affairs, R&D IT) to align scope, requirements, acceptance criteria, and success metrics. Ensure compliance with GxP, 21 CF...

We are looking for a highly skilled and experienced Clinical Administrator to join our team at Oyster & Pearl Hospitals. The ideal candidate will have a strong background in clinical administration and management, with excellent organizational and communication skills. Roles and Responsibility Manage and coordinate clinical administrative tasks efficiently. Develop and implement effective administrative processes to support clinical operations. Collaborate with healthcare professionals to ensure seamless patient care and services. Maintain accurate records and reports of clinical activities and outcomes. Ensure compliance with regulatory requirements and hospital policies. Provide exceptiona...

Role & responsibilities Supervise and ensure smooth operations of the Nursing Department during night hours. Oversee patient care, staff coordination, and compliance with NABH standards . Act as a key link between medical, nursing, and support staff for efficient emergency response. Preferred candidate profile Qualified nursing professional with prior hospital experience. Strong organizational and communication skills. Proven ability to thrive in high-pressure, fast-paced environments. Experience: 58 years in a reputed hospital setup.

Role & responsibilities : Clinical Administration as Medical Suptd / Dy.Medical Suptd. Preferred candidate profile MBBS with any degree / certification in Hospital Administration, Quality & Audit, with a minimum of 2years and more experience in managing a min of 100 bedded hospital.

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.

Role & responsibilities Independently manage 4-5 projects (CRPL) and 10-15 projects (PM) level with full accountability for quality, timelines, and budgets. Responsibilities include preparing clinical trial documents like clinical study protocols, research participant information sheet & consent forms, Case Report Forms, and Investigators Brochures, as well as preparing CTD modules, Study Plans etc. Negotiate Contracts with Sites including site budgets, evaluate site feasibility data, and overseeing all pre-study and post-study activities. The role will require to support ethics committee and regulatory submissions, maintain liaison with regulatory agencies, provide training to site staff an...

Support the maintenance and optimization of Clinical Operations systems. Collaborate on creating and optimizing training programs related to clinical systems. Act as a backup Clinical Business Administrator for system-related activities including CTMS and eTMF administration. Monitor and ensure adherence to Clinical Operations policies and SOPs to maintain inspection readiness. Assist in identifying process challenges and suggesting technology-driven improvements. Contribute to project plans and system-related activities. Job Requirements Bachelor's degree in science, nursing, or a related field. Minimum 3 years of experience in a Clinical Study Manager role or related GCP procedures work. P...

Senior Clinical Research Associate (Sr. CRA) Location: Ahmedabad (Hybrid) Experience: 56 years (Mandatory oncology monitoring experience) Qualification: Masters in Life Sciences / M.Pharm / Pharm D Job Description We are hiring an experienced Senior Clinical Research Associate with strong hands-on site monitoring experience in oncology clinical trials . The role involves end-to-end site management, monitoring, documentation, and ensuring study compliance as per GCP, NDCTR 2019, SOPs, and protocol. Key Responsibilities Conduct SQV, SIV, IMV, closeout visits, and pre-audit visits. Perform end-to-end site management ensuring protocol, GCP, and regulatory compliance. Perform SDV/SDR, review CRFs...

JOB DESCRIPTION Staff Nurse (ANM/GNM ) Male/Female Location: Globuscure Super Speciality Clinics, Nagpur Role: Staff Nurse / Nursing Assistant Shift: 8 Hours (Morning / Afternoon) Experience: 1–5 years (Freshers are also welcome) Key Responsibilities A. OPD & Clinic Responsibilities Assist doctors during specialty OPDs and minor procedures. Perform vitals: BP, Pulse, SPO2, Temperature, RBS, BMI. Manage OPD flow, triage, sample coordination, and patient records. Conduct injections, dressings, wound care, nebulization. Assist in ECG, PFT, Spirometry, TMT (training will be given). Maintain sterilization, infection control, and BMW segregation. Stock management of consumables, emergency drugs, a...

As a Project Training Coordinator at Covance in Bangalore, India, your role will involve: - Facilitating the creation, revision, or inactivation of all project training requirements in the LMS. - Providing regular updates to project leaders and project coordinators on the status of project-related training requirements. - Monitoring and tracking compliance of study teams to training requirements using LMS reporting capabilities and Excel. - Sending out notifications to team members who are delinquent in completing training requirements. - Escalating repeated delinquent training requirements to project leads. - Assigning and removing role-based curricula to staff members throughout the study....

As a Senior Manager, Clinical Scientist at Bristol Myers Squibb, you will be responsible for the design and execution of assigned clinical trial activities. You will work closely with clinical team members within the assigned project to execute activities associated with the conduct. You may serve as a Clinical Trial Lead for one or more trials and lead or support trial-level activities with necessary supervision. Additionally, you may co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members. **Key Responsibilities:** - Collaborate and liaise with external partners such as Key Opinion Leaders (KOLs) - Seek out and enact bes...

Role Overview: You will be responsible for overseeing and managing the clinical operations of the cardiac rehabilitation program. Your role will involve developing and implementing clinical protocols and guidelines, ensuring high-quality patient care, and leading a multidisciplinary team of health professionals. You will also be required to conduct performance reviews, supervise patient assessments, and drive patient engagement to enhance efficacy. Key Responsibilities: - Oversee and manage clinical operations of the cardiac rehabilitation program. - Develop and implement clinical protocols and guidelines in line with best practices. - Ensure high-quality patient care and adherence to clinic...

Responsibilities: Collaborate with healthcare team on patient care plans Ensure compliance with hospital policies & procedures Manage OPD clinics, provide medical services Health insurance Annual bonus Provident fund

As a Pharmacovigilance Associate at Amneal, your role involves daily case intake from various systems, ensuring all cases are captured and triaged accurately. You will collaborate with cross-functional teams to gather necessary information for report completion, participate in training sessions to enhance your understanding of safety regulations, and support the development of SOPs related to ICSR business processes. Additionally, you will assist in training junior staff, support audits and inspections, and maintain comprehensive documentation. Key Responsibilities: - Daily intake of cases from multiple systems and triaging - Reconciliation of cases with vendors and interfaces - Collaborate ...

responsible for overseeing the daily operations of a hospital or healthcare facility. Manage the clinical and administrative staff, including physicians, nurses, technicians, and support staff. Develop and implement policies.

As an Operational Manager, you will be responsible for overseeing all hospital operational areas, including clinical services, general administration, housekeeping, security, facilities, and biomedical support. Your key responsibilities will include ensuring optimal utilization of hospital resources such as staff, equipment, and infrastructure. You will also be monitoring performance and ensuring the delivery of services in line with set quality benchmarks and NABH accreditation standards. - Oversee all hospital operational areas - Ensure optimal utilization of hospital resources - Monitor performance and ensure service delivery as per quality benchmarks In the role of Operational Manager, y...

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 y...

You will be responsible for overseeing the clinical operations at Lyxaa's Calicut center. Your role will involve interpreting diagnostics, supervising treatment protocols, and collaborating with multidisciplinary teams to implement effective health optimization strategies. In addition, you will work closely with the internal technology team to ensure the accuracy and safety of all digital tools and health insights. Key Responsibilities: - Conduct patient consultations, both in-person and virtually - Design and approve personalized wellness and IV therapy plans - Interpret results from blood tests, gut microbiome, epigenetic panels, and wearables - Supervise clinical activities, guide nursing...

Role Overview: As the Hospital Operations Manager, you will be responsible for overseeing the daily operations of all clinical and non-clinical departments. Your role involves monitoring patient flow, admission/discharge processes, and waiting times to ensure efficient operations. You will also be in charge of ensuring the availability of medicines, consumables, and equipment necessary for providing quality patient care. In terms of Patient Experience, you will supervise the front desk, admissions, billing, and customer service teams to address patient grievances promptly and maintain high-quality patient care. Key Responsibilities: - Supervise daily operations of clinical and non-clinical d...

Interact with the US health insurance companies (Insurance Customer Care/Nurses/UM Team) Quality of Notation, Ability to read clinical documentation and data enter for payer requirements. Would secure relevant information of Health Insurance of the patient. Work on Websites/Applications to perform the activity as per the SOP. Would be working in 6pm to 3 am & 9pm to 6am, Supporting US operations (in EST Zone) Should be Open to Learn & adapt as per the changing needs of the process. Will have to go thru ongoing Trainings (for performance / process needs) Should be flexible to be moved across the processes assigned by the Manager (Cater to ongoing process requirements) Will have to work as per...