8317 Clinical Research Jobs - Page 25

Role Overview: As a Medical Affairs professional at Pfizer, your role involves providing scientific expertise and building relationships with Key Opinion Leaders to advance medical practice and research for the benefit of society. By actively contributing to the organization, you will take responsibility for ensuring the scientific, technical, and ethical soundness of all policies, statements, and endeavors. Your focus will be on delivering high-quality and timely service in various areas such as Interactions with Healthcare Professionals, Continuing Medical Education, Clinical Research, Sales Force Training, and support for New Product Development, Regulatory Affairs, Quality Standards, and...

As a Clinical Research Trainer at PMCTI (Pune Medical Coding Training Institute), your role involves delivering training sessions on Clinical Research, GCP (Good Clinical Practice), Regulatory Affairs, Pharmacovigilance, and related topics. You will be responsible for designing, updating, and improving training materials, presentations, and assessments. It will be your duty to assess and evaluate trainees" understanding through tests, assignments, and practical exercises. Staying updated with the latest industry trends, guidelines, and regulatory changes is essential. You will conduct both classroom and online training sessions as per company requirements and provide career guidance and ment...

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As a Feasibility Lead in Business Development, your role will involve driving country and site feasibility activities for early-phase clinical trials. You will be responsible for analyzing feasibility data, engaging with internal teams and external clients, and providing strategic recommendations to support study planning and proposal development. Your position will play a critical role in aligning feasibility operations with scientific, operational, and regulatory goals across global regions. **Key Responsibilities:** - Act as the go-to expert for feasibility practices across therapeutic areas. - Provide strategic input on site and country selection during protocol development. - Stay updat...

Role & responsibilities Assist in the compilation of the study related documents during the pre-trial period Assist site investigator with EC submissions, follow-up & approvals Ensuring site setup according to protocol Update investigator with all study related activities performed Coordinate subject visits Fix appointments for scheduled and unscheduled subject visits as per protocol after prior discussion with site investigator Explain study and related procedures/requirements to subjects Resolving subjects non medical queries Assist in the process of administering the informed consent to the potential Subjects and discussing in detail the patient information sheet Ensure that site document...

As the Head of Research AI at a company focusing on Healthy Aging through AI, your role involves leading AI research and clinical research projects to develop cutting-edge AI solutions. You will be responsible for driving innovation in AI technologies and applications in the healthcare industry. Key Responsibilities: - Lead AI research projects and clinical research studies to advance the development of AI solutions. - Collaborate with a multidisciplinary team to design and implement AI algorithms for medical imaging analysis. - Contribute to the development and optimization of AI models for chest X-ray, CT, and MRI image interpretation. - Stay updated with the latest advancements in AI tech...

Role Overview: As a Clinical Research Associate at Clinogenesis Research Organization, you will have the opportunity to kickstart your career as a Clinical Research Coordinator. This role is specifically designed for fresh graduates who are passionate about clinical research and eager to develop in a structured and accredited environment. Your primary responsibility will be to assist with on-site coordination of clinical trial activities under supervision, ensuring compliance with protocol requirements and ethical standards. Key Responsibilities: - Assist with on-site coordination of clinical trial activities under supervision - Maintain essential documents, site files, and case report forms...

As an experienced medical writer, your role will involve writing high-quality CTD modules including nonclinical and clinical overviews & summaries such as Module 2.5, 2.4, 2.7 as per the EU submission requirements. You will also be responsible for responding to clinical deficiencies, assisting in drug development strategy, updating SmPC, Patient information leaflet, CCDS, Safety variations, preparing clinical study reports, study design, and synopsis. Additionally, you will play a key role in the clinical development strategy, review of study reports, published papers, literature search, and regulatory evaluation. Your expertise will be crucial in Rx to OTC evaluation, PSURs, PADER, and RMP....

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...

Role Overview: You are required to work as a full-time on-site Cardiothoracic and Vascular Surgeon (CTVS) at Apollo Hospitals in Kakinada. Your responsibilities will include performing complex cardiac, thoracic, and vascular surgeries, managing preoperative and postoperative care for patients, collaborating with a multidisciplinary medical team, and actively contributing to the enhancement of clinical practices. Staying abreast of the latest developments in cardiac care and engaging in research and academic activities will also be part of your role. Key Responsibilities: - Perform complex cardiac, thoracic, and vascular surgeries - Manage preoperative and postoperative care for patients - Co...

As a Life Sciences - Pre-Sales Specialist at our company, you will be a key player in supporting sales initiatives within the pharmaceutical, biotechnology, and medical device sectors with a focus on commercial analytics and R&D. Your role will involve establishing Tredence as an industry subject matter expert by leveraging your technical expertise, industry knowledge, and exceptional communication skills. Key Responsibilities: - Support account team and partner sales in conducting detailed discovery sessions to understand client requirements and pain points. - Deliver compelling solution demonstrations showcasing the value of analytics, AI/ML, and data-driven insights for life sciences comm...

Role Overview: As a Medical Writer II (CSR Narrative exp Only) at Syneos Health, a leading fully integrated biopharmaceutical solutions organization, your role involves translating unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. In this position, you will play a crucial role in the Clinical Development model by placing the customer and patient at the forefront of all activities. Your contributions will focus on simplifying and streamlining work processes to enhance both internal and external collaboration for customer success. Key Responsibilities: - Mentoring less experienced medical writers on projects when necessary - Compiling, ...

As a Senior Regulatory Start Up Associate at Novotech, your role will involve planning, preparing, and reviewing country and site level ethics and regulatory authority applications and submissions during project start-up. Your responsibilities will include: - Serving as the primary point of contact for the Regulatory Start-Up Manager (RSM) and/or Project Manager (PM) on allocated projects. - Providing expertise and guidance on country and local regulations, keeping abreast of developments and changes in regulations. - Working within the scope of relevant SOPs and ICH-GCP guidelines. - Providing country and site level information on submission deadlines and timeline metrics. - Ensuring compli...

Job Overview Serve as a therapeutic and/or operational expert throughout the new business and program/project delivery lifecycle. Essential Functions Accountable and responsible for creating effective delivery strategies and solutions for large, complex, multi-service, multi-region studies or programs may include mega studies, addressing the specific needs and challenges of each customer and differentiate IQVIA from its competitors. In partnership with Sales, Medical, Operations, and other functions, responsible for award of strategic and tactical new business to achieve annual Gross New Business targets. Act as champion for project centricity within the organization through enabling the pro...

Accounts Receivable Associate - India, Chennai - 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 an Accounts Receivable Associate to join our diverse and dynamic team. The Accounts Receivable Associate will interact with Project Managers, Contracts Analysts and other departments in order to generate timely and accurate monthly invoices in accordance with the contract terms. The candidate will have a successful background of Contract to Cas...

Ops Support Analyst I, IRT (Customer Service with Voice Process) - Chennai/Trivandrum 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 an Ops Support Analyst I, IRT to join our diverse and dynamic team. As an Ops Support Analyst I, IRT at ICON, you will play a key role in supporting Interactive Response Technology (IRT) systems for clinical trials. You will assist in system troubleshooting, data management, and ensure that IRT solutions operate efficiently, con...

Solution Design and Architecture: Design integration architectures within larger products modules. Improve re-usability by looking for reusing less amount of different components for the same purpose, standardizing over less, "better" ones. Help in selecting the best module for a specific use-case. Analyze the current tech composition and suggest ways for improving it by adhering to Architects team principles. Technical Advisement: Act as a primary technical advisor to development teams, providing insights on how various solutions can be customized and integrated. Research on new technologies and modules and test their suitability for the purpose. Build First of Kind implementations (PoC) an...

Clinical Data Science Associate 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 Clinical Data Science Associate to join our diverse and dynamic team. As a Clinical Data Science Associate at ICON, you will play a key role in analyzing and interpreting clinical trial data, providing valuable insights that support our research efforts. You will contribute to the success of our clinical programs by applying data science techniques to enhance data quality and dri...

Sells and promotes company products within a defined geographic territory by developing new accounts and expanding usage of company products by current accounts in an effort to meet a sales quota based on company sales goals and to directly increase sales revenue of the company. Key Responsibilities Sells products by scheduling sales calls to meet with current and potential customers to fulfill revenue and unit growth objectives assigned by company on a monthly/quarterly/annual basis. Develops and implements sales strategies by determining the relevant factors (e. g. , product, competition and pricing needs) of existing and potential accounts to effectively promote the companys products to a...

Provides high quality, timely development and on-time input to solutions for service delivery, managed services, or implementation oriented client projects. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions to leading small teams. Contributes to meeting client satisfaction objectives. Develops modules and low level designs while monitoring technical quality standards of onshore / offshore developers. Essential Functions Supporting the design and build of new technology solutions including; understanding business needs, determining product specifications, production timetables, pricing, and time-integrated plans f...

As a Medical Scribe , you will assist healthcare providers in accurately documenting patient interactions and maintaining electronic health records. Your primary responsibility is to capture, transcribe, and update medical information during patient visits, ensuring accuracy, completeness, and compliance with medical documentation standards. This role requires strong attention to detail, proficiency in medical terminology, and the ability to work collaboratively in a clinical documentation environment. Candidates passionate about healthcare, quick learners, and those keen to grow in the medical field are ideal for this role. Roles & Responsibilities: Provide real-time scribing of patient cha...

About The Role PharmacovigilanceB.Pharm / M.Pharm graduate with experience in case processing in ARGUS, experience in global submission to Health authorities. Details Location Mumbai Experience 1 - 4 years’ relevant experience in Pharmacovigilance Job Function Business Process Services Role Executive Desired Skills Pharmacovigilance | LS - Pharmacovigilance Qualifications B.Pharm / M.Pharm / BHMS / BAMS / BDS / MSc (Biotechnology, Zoology)

Tablets India Ltd. is looking for Marketing Executive (Medical Representative) to join our dynamic team and embark on a rewarding career journey Develop and maintain relationships with healthcare professionals and organizations Promote and sell our medical products and services to targeted customers Provide product demonstrations and education to customers Attend industry events and conferences to network and stay up to date on industry trends Maintain accurate records of sales activities and customer interactions Achieve sales targets and quotas Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. W...

Tablets India Ltd. is looking for Marketing Executive (Medical Representative) to join our dynamic team and embark on a rewarding career journey Develop and maintain relationships with healthcare professionals and organizations Promote and sell our medical products and services to targeted customers Provide product demonstrations and education to customers Attend industry events and conferences to network and stay up to date on industry trends Maintain accurate records of sales activities and customer interactions Achieve sales targets and quotas Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. W...

Title: Global Lead Statistical Programmer Business Unit: Global Development Biometric Sciences (GDBS) Job Grade Manager Location: Mumbai / Gurugram / 100% remote for the right candidate Key Responsibilities At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive tog...