8317 Clinical Research Jobs - Page 26

Role & responsibilities Drive business development for late-phase and RWE services in assigned global territories (US/EU/APAC). Identify, engage, and convert new clients (pharma, biotech, medical device companies) seeking post-marketing and observational study solutions. Lead end-to-end proposal development, including scope definition, pricing strategy, and bid defense presentations. Partner with Lambdas scientific, medical, and operational teams to ensure feasibility and alignment of proposals with delivery capabilities. Maintain in-depth understanding of industry trends, regulatory frameworks (e.g., EMA, FDA post-marketing requirements), and client needs in the RWE and late-phase space. Re...

We are looking for skilled Regulatory Specialists to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in regulatory affairs and be able to ensure compliance with relevant laws and regulations. Roles and Responsibility Develop and implement regulatory strategies to achieve business objectives. Conduct thorough reviews of existing regulations and identify areas for improvement. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Prepare and submit regulatory documents, such as applications and reports. Monitor and analyze changes in regulatory environments that could impact the company. Provide traini...

We are looking for talented biomedical researchers to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in biomedical research and development, with excellent analytical and problem-solving skills. Roles and Responsibility Conduct experiments and collect data to test new medical devices and treatments. Analyze and interpret complex data sets to identify trends and patterns. Develop and implement new research protocols and procedures. Collaborate with cross-functional teams to design and develop new products. Prepare and present research findings at conferences and workshops. Stay up-to-date with the latest developments in the field of bio...

We are looking for talented biomedical researchers to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in biomedical research and development, with excellent analytical and problem-solving skills. Roles and Responsibility Conduct experiments and collect data to test new medical devices and treatments. Analyze and interpret complex data sets to identify trends and patterns. Develop and implement new research protocols and procedures. Collaborate with cross-functional teams to design and develop new products. Prepare and present research findings to senior management and stakeholders. Stay up-to-date with industry developments and advancem...

We are looking for highly motivated and experienced Clinical Trial Coordinators to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in clinical trials and excellent coordination skills. Roles and Responsibility Coordinate and manage clinical trial activities, including site initiation, monitoring, and close-out visits. Develop and maintain relationships with investigators, sites, and other stakeholders to ensure successful study execution. Prepare and review study protocols, informed consent forms, and other study-related documents. Ensure compliance with regulatory requirements and company policies. Collaborate with cross-functional tea...

We are looking for highly motivated and experienced Clinical Trial Coordinators to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in clinical trials and excellent coordination skills. Roles and Responsibility Coordinate and manage clinical trial activities, including site initiation, monitoring, and close-out visits. Develop and maintain relationships with investigators, sites, and other stakeholders to ensure successful study execution. Manage study timelines, budgets, and resources to achieve project goals. Ensure compliance with regulatory requirements and company policies. Collaborate with cross-functional teams to resolve issues a...

We are looking for highly skilled Regulatory Specialists to join our team at Medblue Innovations Private Limited. The ideal candidate will have a strong background in regulatory affairs and be able to ensure compliance with relevant laws and regulations. Roles and Responsibility Develop and implement regulatory strategies to achieve business objectives. Conduct thorough analysis of regulatory requirements and provide expert advice. Collaborate with cross-functional teams to ensure compliance with regulatory standards. Prepare and review regulatory documents, such as applications and reports. Stay up-to-date with changes in regulatory requirements and advocate for updates. Provide training an...

Role & responsibilities Develop and manage comprehensive project plans, including timelines, budgets, resource allocation, and risk mitigation strategies. Oversee all aspects of trial startup, including site selection, contract negotiation, IEC/IRB submissions, and study team training. Monitor trial progress against established milestones and timelines, proactively identifying and addressing potential delays or roadblocks. Manage project budgets, track expenses, and ensure cost-effectiveness. Collaborate with cross-functional teams (e.g., medical, biostatistics, data management, regulatory) to ensure seamless project execution. Manage vendor relationships, including selection, contract negot...

Role Overview: As a Medical Oncologist DM DNB Consultant, you will play a crucial role in the diagnosis, treatment, and management of patients with cancer. Your expertise and decision-making will directly impact patient outcomes and contribute to the advancement of medical oncology. You will be responsible for conducting thorough patient assessments, developing comprehensive treatment plans, administering chemotherapy and other oncology treatments, and monitoring patient responses to treatment. Additionally, you will participate in clinical research, contribute to medical advancements in oncology, and collaborate with multidisciplinary teams to provide holistic patient care. Your role will a...

As a Medical Expert in Translational Clinical Oncology (TCO) at Novartis, your role involves serving as the medical leader for assigned global, roll-over, and long-term follow-up studies, as well as studies in the close-out phase. You may also provide medical co-leadership for specific aspects of global TCO studies under the guidance of a Clinical Program Leader (CPL). Key Responsibilities: - Provide medical support to the CPL and contribute to clinical sections of protocols, Informed Consents, publications, and regulatory documents. - Review clinical trial data and oversee program safety reporting. - Represent the CPL at project team meetings and Investigator teleconferences. - Lead the rev...

As a Senior Clinical Data Manager I at Allucent, your role will involve leading data management activities within the Allucent Data Management (DM) department. You will be responsible for ensuring the completeness, accuracy, and consistency of clinical data to meet quality standards and regulatory requirements for analysis and reporting. Additionally, you will provide expertise in data management areas, develop departmental processes, tools, and train staff. This position is based in Bengaluru. **Key Responsibilities:** - Lead and serve as the primary contact for data management with internal and external parties. - Plan resources, manage tasks, timelines, risks, and quality. - Develop, revi...

Preparing Study Audit Plan Develop audit plans for BA/BE and Phase I studies in consultation with senior personnel. Conducting Study Audits Perform in-process and retrospective audits of Clinical and Statistical phases in consultation with senior personnel. Preparation & Issuance of Audit Reports Prepare and issue audit reports (in-process and retrospective) for Clinical and Statistical phases with guidance and review from senior personnel. Compliance Verification Assist seniors in verifying compliance of audit responses and ensure closure of audit reports. Review of Study Reports Review draft and final study reports for accuracy and compliance. Issuance of QA Authentication Issue QA authent...

Review medical charts, physician notes, and clinical documentation. Assign accurate ICD-10-CM , CPT , and HCPCS codes based on guidelines. Ensure coding accuracy and compliance with industry standards and payer regulations . Verify patient information and ensure completeness of medical records. Work with team leaders to resolve coding discrepancies. Maintain strict confidentiality of patient health information (HIPAA compliance). Basic knowledge of anatomy , physiology , and medical terminology . Strong attention to detail and analytical skills. Good communication and documentation skills.

Role Summary The Manager Business Development will lead client engagement, drive revenue growth initiatives, and oversee the end-to-end business development function. This role requires a strategic thinker with strong leadership abilities, excellent client management skills, and the capability to coordinate cross functionally to support organizational growth. The Manager will supervise BD Executives, ensure pipeline development, and serve as a key liaison between clients and internal teams. Key Responsibilities Client Management & Relationship DevelopmentBuild, nurture, and strengthen long-term relationships with clients and strategic partners.Conduct client / service provider meetings, pres...

This Position reports to: Delivery Manager-Tax Operations Roles and Responsibilities: The individual will be responsible for overseeing end-to-end compliance for both Indirect and Direct Taxes for multiple countries. This role will be reported directly to the Tax Operations Delivery Manager. Seeking a detail-oriented and proactive Tax Operations Specialist / Sr. Specialist to support the accurate and timely execution of tax-related processes across our organization. This role involves managing tax documentation, ensuring compliance with regulatory requirements, supporting tax reporting, and collaborating with internal and external stakeholders to streamline operations. Tax Documentation & Co...

We are looking for a highly skilled and experienced Global Feasibility Coordinator to join our team in Bangalore. The ideal candidate will have 2-5 years of experience in feasibility analysis, project management, and coordination. Roles and Responsibility Coordinate with cross-functional teams to ensure successful project execution. Conduct feasibility studies and analyze data to identify trends and opportunities. Develop and implement project plans, resource allocation, and risk management strategies. Collaborate with stakeholders to gather requirements and provide updates on project progress. Identify and mitigate potential risks and issues impacting project timelines or budgets. Ensure co...

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...

EC Submission To get the documents from Central Drive, print, prepare files accordingly, and dispatch them to the respective sites prior to the Ethics Committee meeting conducted at site. SIV (Site Initiation Visit) Kits Preparation To co-ordinate with CRD and prepare the SIV kits, study related material (NS Bottle, Syringe & Needle, Instrument- Digital clock, thermo hygrometer, Data logger, Infusion Pump) and dispatch to the site before the Site Initiation Visit. Logistics Activities To arrange the IMP (Investigational Medicinal Product) shipments at the site, coordinate with the Pharmacist Team & logistics vendor before patients randomize the study. To arrange the PK sample (Blood Sample) ...

Primary Responsibilities: 1. Off-site Monitoring Undertake off-site visits during different phases of the study period. Conduct Initial Site Visits as per the study plan to train and guide site personnel. Inspect pre-requisites as per protocol and ensure the site is ready for the study. Perform routine monitoring visits at predetermined frequencies as per study guidelines. 2. Communication & Documentation Communicate with potential sites for Feasibility Assessment Questionnaires and obtain required details for review. Follow up regularly with off-site nodal personnel/in-charge and prepare visit reports (Pre-study Qualification Report, Site Initiation Visit Report, Site Monitoring Visit Repor...

The Sr Manager, CSS is responsible for strategic and operational leadership of multiple Managers within Centralized Study Support (CSS). This role ensures delivery of high quality centralized operational support across clinical programs and alignment of resources with organizational priorities. Roles & Responsibilities: Team Management Provide leadership, direction and mentorship to multiple Managers, Centralized Study Support. Set strategic goals for the team in collaboration with Sr Mgr colleagues and in alignment with corporate objectives Ensure consistency in management practices, performance standards and staff development approaches across all managers. Monitor functional performance a...

DNB Program Responsibilities Manage DNB program, admissions, and NBE accreditation. Handle trainee registration with NBE. Guide students throughout the course. Conduct internal/external exams. Coordinate with HODs and manage library records. Perform management-assigned tasks; must have good communication skills and be flexible to travel. Clinical Research Responsibilities Oversee planning and execution of all clinical trials at Fortis Hospital, Manesar. Ensure site readiness, protocol compliance, and resource allocation. Develop SOPs and maintain quality systems. Ensure adherence to ICH-GCP, Schedule Y, NDCT rules, and SOPs. Manage submissions to EC and regulatory bodies. Coordinate with Inv...

Role Description: The Manager, CSS is accountable for hiring, managing, mentoring and growing a team of Study Delivery Associates and Sr Associates. The role is accountable for continually developing the CSS roles within their team, ensuring they are positioned to deliver high-quality operational support to clinical programs and managing performance issues effectively and compassionately. Roles & Responsibilities: Team Management Recruit, onboard and train (in partnership with R&D Training) new team members to meet current and future program needs Provide regular mentoring, coaching and competency development support for all direct reports Proactively manage team risks, including attrition a...

Role Description: The Manager, CSS is accountable for hiring, managing, mentoring and growing a team of Study Delivery Associates and Sr Associates. The role is accountable for continually developing the CSS roles within their team, ensuring they are positioned to deliver high-quality operational support to clinical programs and managing performance issues effectively and compassionately. Roles & Responsibilities: Team Management Recruit, onboard and train (in partnership with R&D Training) new team members to meet current and future program needs Provide regular mentoring, coaching and competency development support for all direct reports Proactively manage team risks, including attrition a...

Role GCF: 5 ABOUT THE ROLE Role Description: The Manager, CSS is accountable for hiring, managing, mentoring and growing a team of Study Delivery Associates and Sr Associates . The role is accountable for continually developing the CSS roles within their team, ensuring they are positioned to deliver high-quality operational support to clinical programs and managing performance issues effectively and compassionately . Roles & Responsibilities: Team Management Recruit, onboard and train (in partnership with R&D Training) new team members to meet current and future program needs Provide regular mentoring, coaching and competency development support for all direct reports Proactively manage team...

As a Senior Medical Writer at MS Clinical Research Pvt Ltd, you will be responsible for creating high-quality, scientifically accurate medical documents to support clinical trial activities and regulatory submissions. Your role will involve preparing and reviewing clinical study protocols, reports, and other trial documents in compliance with regulatory guidelines and industry standards. Additionally, you will collaborate with cross-functional teams, interpret clinical trial data, assist in regulatory submissions, and contribute to project planning and timelines. Key Responsibilities: - Prepare and review clinical study protocols, reports, and other trial documents following regulatory guide...