799 Clinical Operations Jobs - Page 9

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

OVERALL PURPOSE OF THE ROLE: The Line Manager Is responsable to support the Operations Manager to deliver the service demandes of the DEPOT by leading and facilitating effective team working among the team members for servicing / planned maintennece and renovation/modernisation/corrective maintenance activity. The purpose of the job is to Manage all the maintenance activities (PM/ CM/ A&V) in the Line/Workshop including the responsibilities linked to the position as hierarchical manager of the employees of the Maintenance organization who belong to this Line/Workshop. RESPONSIBILITIES: Team Management Lead all aspects of the team in the maintenance, servicing to meet customer requirements wi...

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 ...

Greetings from Wipro!! We are inviting applicant for Walk-in Drive-in Pune Location for Pharmacovigilance Experience- 1 to 2 years Qualification- B. Pharm/ M. Pharm with valid Pharma license Only the qualifications mentioned are eligible Candidate should have excellent Communication in English Should be ready for Rotational shifts Should have excellent knowledge of Pharmacovigilance Should be ready to work from office Should be ready to relocate to Pune Walk In Date- 4-Nov -25 Time to Report- 10.00 A.M- 12.30 P.M Documents to carry- Update CV & original govt. ID Card. Should mention at the top of the CV the source of information about the walk-In Walk in Address- Unit 2, Plot No 31, Hinjewad...

As a Data Analyst at Agilisium, your role will involve gathering, validating, and analyzing data from clinical, operational, and administrative systems. You will be responsible for building interactive reports and dashboards using tools like Power BI, Tableau, or similar platforms to present insights to leadership and stakeholders. Additionally, you will generate routine and ad hoc analytical outputs to support business decisions and performance reviews. Key Responsibilities: - Gather, validate, and analyze data from various systems - Build interactive reports and dashboards using Power BI, Tableau, or similar tools - Generate routine and ad hoc analytical outputs - Develop and monitor Key P...

This role involves the creation and validation of clinical study datasets, ensuring compliance with CDISC SDTM standards. The candidate will collaborate with cross-functional teams to support clinical data transfer.

We are looking for a highly skilled and experienced Associate - Clinical Documentation Improvement Specialist to join our team at Future Healthcares. The ideal candidate will have 1 to 6 years of experience in clinical documentation improvement. Roles and Responsibility Develop and implement effective clinical documentation improvement strategies to enhance patient care. Collaborate with healthcare professionals to identify and resolve issues related to clinical documentation. Analyze data to identify trends and areas for improvement in clinical documentation. Design and deliver training programs to educate healthcare staff on best practices for clinical documentation. Monitor and evaluate t...

Position Summary The Wellness Head is responsible for overseeing the Health & Wellness operations across all communities, ensuring standardized medical, clinical, and wellness practices are implemented in alignment with company and medical directorate guidelines. This role ensures consistent delivery of high-quality care, operational efficiency, and compliance with all health, safety, and statutory standards, while driving continuous improvement and resident satisfaction. Key Interactions Internally: Chief Medical Superintendent Resident Managers / Assistant Resident Managers Nursing, Physiotherapy, and Clinical Teams Operations,F&B, Housekeeping, and Maintenance Departments Corporate HR, Fi...

Job Summary: We are looking for a compassionate Nurse Nursing Care professional to provide patient care and assist in clinical operations The role involves administering medications, monitoring patient conditions, and coordinating with doctors and staff Key Responsibilities: Provide nursing care to patients as per medical guidelines Administer medications, IVs, and injections as prescribed Monitor and record vital signs and patient progress Maintain patient records and ensure timely reporting Support doctors during rounds and procedures Follow infection control and hospital safety policies

Job Title: Centre Manager Department: Operations / Administration Reports To: Regional Operations Head / Medical Director Location: Faridabad Job Summary: The Centre Manager will oversee the daily operations of the IVF Centre, ensuring smooth functioning of all clinical and non-clinical activities. The role involves managing staff, maintaining service quality, ensuring patient satisfaction, driving revenue targets, and ensuring compliance with medical and legal standards. Key Responsibilities: 1. Operations Management Oversee day-to-day operations of the IVF Centre to ensure seamless patient flow and efficient service delivery. Coordinate between clinical, nursing, embryology, and administra...

• Manage front office, appointments, and patient/client coordination • Answer calls, respond to messages, handle email queries • Take product orders and ensure prompt dispatch • Assist with day-to-day operations Handling company social media Required Candidate profile Must be fluent in English ( spoken and written), Hindi, and Tamil – both spoken , • Prior experience in clinical reception/admin or e-commerce backend • Familiar with basic computer/email operations Perks and benefits Accommodation support hostel(3,500)

Diagnose and provide appropriate dental treatment to patients, including regular cleanings, fillings, root canals and cosmetic dentistry. Carefully document all medications, diagnoses & treatments Excellent communication skills (English).

JOB DETAILS 1 Develop and maintain in-depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance/ participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/international literature. 2 Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department (i.e. medical information packs, clinical expert reviews, etc). 3 Establish and maintain professional and credible relationsh...

JOB DETAILS 1 Develop and maintain in-depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance/ participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/international literature. 2 Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department (i.e. medical information packs, clinical expert reviews, etc). 3 Establish and maintain professional and credible relationsh...

JOB DETAILS 1 Develop and maintain in-depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance/ participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/international literature. 2 Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department (i.e. medical information packs, clinical expert reviews, etc). 3 Establish and maintain professional and credible relationsh...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee. 2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4) Liaise with ethics committee regarding rights, safety and well-being of trial subjects. 5) Ordering, tracking, and managing IP and trial materials. 6) Overseeing and documenting IP dispensing, inventory and reconciliation. 7) Protecting subjects confidentiality, updating their information, and verifying IP has been dispensed and administered according to protocol. ...

JOB DETAILS 1. Prevent the payment of potentially fraudulent and/or abusive claims utilizing medical expertise, knowledge of CPT/diagnosis codes, CMC guideline along with referring to client specific guidelines and member policies 2. Adhere to the state and federal compliance policies and contract compliance 3. Assist the prospective team with special projects and reporting 4. This process works on identifying discrepancies between medical records and billed services 5. Identifying Up-coding, Duplication, and Misrepresentation of services 6. Managing and reporting adverse events and serious adverse events 7. Reviewing clinical study protocols, reports and study documentations 8. Supervising ...

A Centre Head in a hospital setting is essentially a department manager, responsible for overseeing the day-to-day operations of a specific clinical or administrative unit within the hospital, including managing staff, budgets, quality standards, patient care delivery, and ensuring smooth operations within their designated area, while reporting to higher management; key responsibilities include: staff Supervision, Operational Management,Operational Management etc. Managing day to day operation work

As a Senior Clinical Operations Specialist (Senior CTA) at Syneos Health in Athens, you will play a crucial role in ensuring compliance with Corporate and Clinical Operations Policies, Standard Operating Procedures, and Work Instructions. Your responsibilities will include: - Assisting Clinical Monitoring staff with site management activities, acting as a Sponsor representative for assigned sites, and ensuring compliance with protocol requirements and study procedures. - Creating and maintaining project files, handling project correspondence, and participating in file audits. - Preparing and updating site manuals, reference tools, and other documents. - Inputting clinical tracking informatio...

Collaborate with cross-functional teams to ensure successful clinical trial execution.Provide medical expertise and guidance on clinical trial protocols and procedures.Conduct thorough reviews of clinical trial data and reports to identify trends Required Candidate profile Strong understanding of clinical trials, including design, conduct, and analysis.Excellent communication and interpersonal skills, with the ability to work effectively with diverse groups.

Manage and oversee the development, implementation, and maintenance of clinical data management systems.Collaborate with cross-functional teams to ensure accurate /timely delivery of clinical data.Develop and implement data quality control process Required Candidate profile Strong knowledge of Veeva EDC and clinical data management principles.Excellent analytical and problem-solving skills with attention to detail.Ability to work effectively in a team environment

Conduct quality control checks on data accuracy and completeness.Provide training and support to staff on data management best practices.Ensure timely delivery of high-quality data products to stakeholders. Required Candidate profile Strong understanding of clinical trial operations and regulations. Experience with data management systems and software applications. Excellent analytical and problem-solving skills

Conduct thorough medical reviews of device-related documents to ensure compliance with regulatory requirements.Collaborate with cross-functional teams to identify and resolve issues related to medical documentation. Required Candidate profile Strong understanding of medical terminology and regulations governing the device industry. Ability to work effectively in a team environment and communicate complex ideas clearly.

About The Role About The Role Job Title - Research & Development Consultant – Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Must have skills:R&D, Pharmacovigilance, regulatory Reporting Good to have skills:Core LS consulting Job Summary :MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire ...

About The Role About The Role Job Title - Research & Development Consultant – Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Job Summary :MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire and analysis, operating model, business process mapping, and so on. Preferably worked with R&D functi...