6710 Clinical Research Jobs - Page 41

Consultant Pathologist Mumbai Lab Operations Role summary Overall Operations and ensuring that the lab develops and uses a quality system approach to laboratory testing. What the role entails Key accountabilities/ responsibilities Ensure accurate and timely reporting of test results on samples that are fit for examination Ensuring all the required reports are delivered as per the TAT. Support Internal and external client s scientific needs Ensure the laboratory develops and uses a quality system approach to laboratory testing to provide accurate and reliable tests results, Involve QA Assessments Ensure safety measures such as Physical, Chemical and Biological Hazards are followed to ensure s...

- Develop & Execute regulatory strategies - Stay updated on evolving global regulatory requirements & ensure products comply with international standards - Collaboration with Cross functional teams including R&D, QA, Clinical developments. Required Candidate profile - Strong leadership & management skills, including experience leading cross functional teams - Proven track record of successful regulatory submissions & approvals

We are looking for a highly skilled and experienced Finance Compliance Manager to join our team at Sheraton Grand Bengaluru. The ideal candidate will have 1-3 years of experience in finance compliance. Roles and Responsibility Manage and oversee financial compliance with regulatory requirements. Develop and implement effective compliance programs to mitigate risks. Conduct audits and reviews to ensure adherence to financial regulations. Collaborate with cross-functional teams to identify and resolve compliance issues. Provide training and guidance on compliance matters to staff members. Monitor and report on compliance performance metrics. Job Requirements Strong knowledge of financial regul...

About the role: Team Leader To work with the business to understand and manage Programs being run for the Clients/Brands. And for accelerating the core growth metrics focusing on sales & distribution. Provides guidance and instruction to a working group about a project or portfolio of projects. These leaders are responsible for monitoring the efforts of the team members and getting the work done effectively and efficiently with the proper utilization of resources. Skills that will help you succeed in this role: 2+ yrs. of experience in Distribution sales in fintech, Banking/ Sales, EDC Sales. Develop plans and strategies for developing business and achieving the company's sales goals. Create...

We are currently seeking an experienced Global Regulatory Program Manager to help manage a new internal initiative within Oracle Health.In this critical role, you will help drive definition and clarity around customer excellence, specifically focusing on leveraging regulatory knowledge and technical expertise to ensure Oracle Health compliance is met on documentation required for conformity on all Oracle Health products deemed a medical device. The outcomes of this role are to define, measure, and hold Oracle Health product teams accountable to the newly defined operational bar established for global regulatory technical compliance. You will be specificallyresponsible for the successful mana...

Site Name: Bengaluru Luxor North Tower Posted Date: Oct 29 2025 Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients needs and have the highest probability of success. We're uniting science, technology, and talent to get...

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 products relevant therapeutic areas through attendance participation at key internal meetingstraining sessions, relevant congresses, and seminars and by regular self-study of the nationalinternational literature. 2)Provide expert medicalscientific advice for assigned products and related therapeutic areas, including responding to requests for scientifictechnical 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 relationships with ke...

JOB DETAILS 1.Be the medical expert for the therapy area and the medical lead within the brand team inputting into the strategy for the brand 2.Support the Medical Director in carrying out the day to day operational activities of the Medical Department. 3.Review and sign-off of promotional and non-promotinal material to ensure compliance with the Codes of Practice 4.Provide input to Norgine Global projects as agreed from time to time on a defined basis. 5.Work to ensure compliance in all Norgine UK s procedures including GxP, Codes of Practice and medicines legislation. 6.Support medical affairs projects and activities 7.Maintain high standards of technical proficiency 8.Develop relationship...

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) Work to improve efficiency and quality in delivering healthcare services 2) Keep up to date on new laws and regulations so that the facility in which they work complies with them 3) Supervise assistant administrators in facilities that are large enough to need them 4) Manage the finances of the facility, such as patient fees and billing 5) Create work schedules 6) Represent the facility at investor meetings or on governing boards 7) Keep and organize records of the facilitys services such as the number of inpatient beds used 8) Communicate with members of the medical staff and department heads FUNCTIONAL AREA Medical & Health Services Manager, Healthcare manager, Healthcare Ex...

JOB DETAILS 1)Needs to ensure that most of the safety reports that are received from the investigational sites or from the post- marketing sector must be identified & reported in accordance to the ICH-GCP standards & also by the standard operational procedures. 2)Reports that are collected must be organized based on the seriousness or effectiveness of the drug initially. 3)An overall consistency in assessing the adverse reaction reports must be accurate & legible. 4)Must be judgmental in taking appropriate decisions by applying their knowledge of FDA & ICH-GCP standard regulations. 6)Must be able to communicate with clinical physicians in drug safety and assess case report forms. 7)Must be a...

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. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements. 2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines. 3. Review informed consent document / procedures. 4. Negotiate study budgets with potential investigators and assists with the execution of site contracts Provide monitoring visits and site management for a variety of protocols, sites 5. Administer protocol and other study-related training to assigned site personnel and establish regular lines o...

JOB DETAILS 1. Ensure thatclinical researchstudies are conducted in accordance with the protocol, standard operating procedures, goodclinicalpractice (GCP) guidelines, and other applicable regulatory requirements. 2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines. 3. Review informed consent document / procedures. 4. Negotiate study budgets with potential investigators and assists with the execution of site contracts Provide monitoring visits and site management for a variety of protocols, sites 5. Administer protocol and other study-related training to assigned site personnel and establish regular lines of co...

JOB DETAILS 1.writing drug trial methodologies (procedures) 2.identifying and briefing appropriate trial investigators (clinicians) 3.setting up and disbanding trial study centres 4.designing trial materials and supplying study centres with sufficient quantities 5.providing clinicians with instructions on how to conduct the trials 6.collecting and authenticating data collection forms (commonly known as case report forms) 7.monitoring progress throughout the duration of the trial 8.writing reports 9.Commercial awareness 10.A logical and inquisitive mind 11.Good organisational abilities 12.Excellent numerical, written and verbal communication skills FUNCTIONAL AREA Clinical Resaerch, Resaerch ...

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 ...

JOB DETAILS 1.Collaborating with Project Manager to set targets for clinical monitoring staff, and ensuring recording of trial in compliance with project goals. 2.Creating and implementing study-specific clinical monitoring tools and documents. 3.Creating and overseeing trial budget. 4.Identifying, enlisting and choosing sites, and coordinating site management activities. 5.Coordinating and supervising clinical monitoring team. 6.Providing Clinical Research Associates with project-specific training and having regular meetings with them. 7.Recording and sharing interactions with client, and acting as their representative. 8.Arranging and overseeing site visits. 9.Gathering and examining trial...

JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements. 2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines. 3. Review informed consent document / procedures. 4. Negotiate study budgets with potential investigators and assists with the execution of site contracts Provide monitoring visits and site management for a variety of protocols, sites 5. Administer protocol and other study-related training to assigned site personnel and establish regular lines o...

JOB DETAILS 1. Minimum as Graduate in Medicine or other relevant 2. Good knowledge of ICH GCP 3. Demonstrated computer skills (MS Office, MS Project, PowerPoint) 4. Excellent understanding of medical terminology and clinical trial activities 5. 1 - 2 years of experience in clinical practice or academics 6. Excellent written and spoken English 7. Ability to plan well and handle complex tasks simultaneously and independently 8. Analytical and result oriented 9. Good team player with communication and stakeholder management skills 10. Proactive and resilient to changes FUNCTIONAL AREA Medical Reviewer, Associate Medical Reviewer, Medical Reviewer Jobs in Bangalore, Medical Reviewer Jobs in Beng...

We are looking for a highly motivated and dedicated individual to join our team as an Assistant in Imaging Services at Vijaya Diagnostic Centre Limited. The ideal candidate should have 0-1 years of experience. Roles and Responsibility Assist in the operation and maintenance of imaging equipment. Prepare patient samples and materials for imaging procedures. Monitor patient vital signs and reactions during imaging procedures. Maintain accurate records of imaging results and patient information. Collaborate with healthcare professionals to provide high-quality patient care. Participate in quality control and quality assurance activities to ensure excellence in imaging services. Job Requirements...

We are looking for a highly motivated and enthusiastic individual to join our team as a Trainee in Imaging Services at Vijaya Diagnostic Centre Limited. The ideal candidate should have 0-1 years of experience. Roles and Responsibility Assist in the operation and maintenance of imaging equipment. Prepare patient samples and ensure proper handling of medical instruments. Collaborate with healthcare professionals to provide high-quality patient care. Maintain accurate records of patient information and imaging results. Participate in ongoing education and training to enhance skills and knowledge. Ensure compliance with safety protocols and regulations. Job Requirements Strong understanding of b...

We are looking for a highly motivated and dedicated individual to join our team as an Assistant in Imaging Services at Vijaya Diagnostic Centre Limited. The ideal candidate should have 0-1 years of experience. Roles and Responsibility Assist in the operation and maintenance of imaging equipment. Prepare patient samples and materials for imaging procedures. Monitor patient vital signs and reactions during imaging procedures. Maintain accurate records of imaging results and patient information. Collaborate with healthcare professionals to provide high-quality patient care. Participate in quality control and quality assurance activities to ensure excellence in imaging services. Job Requirements...

We are looking for skilled Senior Technicians with 4 to 6 years of experience in CT and MRI to join our team at Vijaya Diagnostic Centre Limited. The ideal candidate will have a strong background in biotechnology, pharmaceuticals, or clinical research. Roles and Responsibility Operate and maintain complex medical imaging equipment such as CT and MRI machines. Prepare patients for procedures and ensure proper patient positioning and immobilization. Administer contrast agents and other medications as ordered by physicians. Monitor patient vital signs and respond to adverse reactions during procedures. Collaborate with radiologists and other healthcare professionals to interpret images and prov...