8317 Clinical Research Jobs - Page 16

Managing Consultant, Advisors & Consulting Services, Strategy & Transformation We provide value-added services and leverage expertise, data-driven insights, and execution. Our Advisors & Consulting Services team combines traditional management consulting with Mastercards rich data assets, proprietary platforms, and technologies to provide clients with powerful strategic insights and recommendations. Our teams work with a diverse global customer base across industries, from banking and payments to retail and restaurants.The Advisors & Consulting Services group has five specializations: Strategy & Transformation, Performance Analytics, Business Experimentation, Marketing, and Program Managemen...

Job Responsibility 1. Development of regulatory clinical documents such as clinical study protocols, investigator brochures, Informed Consent Forms (ICFs), Case Report Forms (CRFs), clinical summaries, and clinical study reports for BA/BE and Phase IIV clinical trials. 2. Extensive knowledge of ICH/GCP guidelines and the pharmaceutical industry to ensure all regulatory documents comply with applicable standards and requirements. 3. Analyze, interpret, and summarize clinical data from various clinical studies with scientific accuracy. 4. Compose patient education materials and lay summaries related to clinical studies. 5. Develop complex scientific content for manuscripts, abstracts, posters,...

We are seeking a highly qualified and experienced Professor Medicine to lead undergraduate and postgraduate teaching, clinical services, and academic activities in the Department of Medicine. The role involves delivering high-quality medical education, mentoring postgraduate students, and contributing to research and institutional development in accordance with prevailing NMC/NBEMS regulations effective from 30 June 2025 . Key Responsibilities: Conduct undergraduate and postgraduate teaching in Medicine. Guide and mentor PG students in academics, research, and clinical practice. Provide advanced patient care as a Senior Consultant in Medicine. Participate in curriculum development, examinati...

Requirement overall – 5 in Medical underwriting. Shifts – Night Shifts || 2 fixed off Location :- Gurgaon/Noida The process would be hybrid and Work from office only. For more info call HR Sanjana@9999129207 https://wa.me/qr/S5CM6Y37H4K6A1 Required Candidate profile Candidate should have exp in US life insurance medical underwriting/ summarization.No Indian Medical underwriting exp will work.We required medical graduates only such as BPT, MPT, BHMS, BDS BAMS, etc

Requirement overall – 5 in Medical underwriting. Shifts – Night Shifts || 2 fixed off Location :- Gurgaon/Noida The process would be hybrid and Work from office only. For more info call HR Sanjana@9999129207 https://wa.me/qr/S5CM6Y37H4K6A1 Required Candidate profile Candidate should have exp in US life insurance medical underwriting/ summarization.No Indian Medical underwriting exp will work.We required medical graduates only such as BPT, MPT, BHMS, BDS BAMS, etc

The Medical Advisor will act as the medicalscientific expert for the organization, supporting global new product launches and lifecycle management Responsibilities include interpreting and communicating clinical data, providing medical review of promotional and non-promotional materials, driving medico-marketing strategies, conducting internal medical training, developing scientific content, and leading KOL/HCP engagement activities The role also involves overseeing evidence generation, supporting investigator-initiated studies, contributing to RWE and publications, ensuring medical information compliance, and collaborating with regulatory, marketing, market access, and commercial teams The ...

The payment processor is responsible for processing investigator grant payments and providing best-in-class customer service to Global Payment Conduct monthly review and analysis of assigned projects, project performance variances, and unbilled/unearned positions Prepare monthly reporting requirements for assigned projects, including unsigned contract opportunities, backlog, and other ad-hoc financial analysis as required Monitor Unbilled, Write-off activity, Over the Limit and Contract Activation exception reports and resolve/escalate unusual activity Review / reconcile loaded project budgets to ensure accuracy against contracted values and compliance to negotiated contract terms Coordinate...

Job Overview The payment processor is responsible for processing investigator grant payments and providing best-in-class customer service to Global Payment Conduct monthly review and analysis of assigned projects, project performance variances, and unbilled/unearned positions Prepare monthly reporting requirements for assigned projects, including unsigned contract opportunities, backlog, and other ad-hoc financial analysis as required Monitor Unbilled, Write-off activity, Over the Limit and Contract Activation exception reports and resolve/escalate unusual activity Review / reconcile loaded project budgets to ensure accuracy against contracted values and compliance to negotiated contract ter...

Essential Functions Consolidate and expand knowledge, experience, and competence in specific Medical Writing tasks by preparing assigned documents to a high standard, with growing independence, focusing on tasks such as writing patient narratives. Manage day-to-day workload, track timelines, draft assigned documents to a high standard, and implement review comments and customer requests with senior guidance/review, keeping manager/senior staff abreast of progress on tasks and any potential problems. Interact with internal clients. May have some external interactions, mostly directed by senior staff. Keep abreast of current data, trends, medical and/or technical writing/regulatory knowledge, ...

External Job Description we need programmers with minimum 10+ years experience with ADaM and TFL programming , Experience in Oncology/Immunology studies on Efficacy ADaMs and TFLs (ADTTE - PFS, OS, DOR, BOR, ORR is must) Experience on KM Plots, waterfall plot, Forest plot is required. Phase 2, 3 Preferable experience. .

Job Overview The Associate Monitoring/Lead (AM) role supports centralized monitoring activities to enhance site performance and data quality across clinical trials. The AM works closely with Site Managers (SMs) by reviewing trial data, identifying early risk indicators, and providing actionable insights. This role is ideal for candidates who are analytical, tech-savvy, collaborative, and confident in influencing without authority Key Responsibilities Conduct ongoing centralized data review to identify trends, risks, and quality gaps. Translate data insights into clear, prescriptive recommendations for Site Managers with expected timelines. Enable SMs by taking on analytic workload, allowing ...

What you will be doing Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements. Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions. Support the preparation of study-related materials, such as informed consent forms and case report forms. Work with cross-functional teams to facilitate communication and ensure smooth trial execution. Contribute to the tracking and reporting of clinical trial metrics and milestones. Your profile Bachelors degree in a scientific or healthcare-related field. Prior experience or strong interest in clinical research. KNwle...

Position Summary The Director, Global Trial Lead (GTL) is accountable for the strategic leadership and operational excellence of global clinical trials, driving delivery across all phases and therapeutic areas. This role sets the vision for successful trial execution, influences organizational strategy, and ensures alignment with business objectives, regulatory standards, and quality benchmarks. Duties/Responsibilities Responsibilities involve a combination of execution and oversight, dependent on the sourcing model, to ensure deliverables and may include, but are not limited to, the following: Project Management Provides leadership and oversight for multiple, complex clinical trials and pro...

The Sr. Associate II, Scientific Education (Professional Path), is primarily responsible for providing analytics support to Alcons internal teams, facilitating data-driven decisions, and designing promotional materials. You will also support Standard Operating Procedure (SOP) creation and engage in knowledge sharing. Specifics include: Provide field support to customers and field staff, conducting on-site education and consulting Establish and maintain customer relations with healthcare professionals and organizations Develop and participate in presentations for conventions, forums, and meetings to raise product awareness Share product information and data analysis with clinical research gro...

The Medical Advisor will act as the medicalscientific expert for the organization, supporting global new product launches and lifecycle management Responsibilities include interpreting and communicating clinical data, providing medical review of promotional and non-promotional materials, driving medico-marketing strategies, conducting internal medical training, developing scientific content, and leading KOL/HCP engagement activities The role also involves overseeing evidence generation, supporting investigator-initiated studies, contributing to RWE and publications, ensuring medical information compliance, and collaborating with regulatory, marketing, market access, and commercial teams The ...

Build partnerships with KOLs & specialists Lead CMEs, webinars & peer programs Drive medical insights, compliance & strategy Collaborate with marketing & access teams Do share your resume at odigostraining@gmail.com Or call 8169631633

Build partnerships with KOLs & specialists Lead CMEs, webinars & peer programs Drive medical insights, compliance & strategy Collaborate with marketing & access teams Do share your resume at odigostraining@gmail.com Or call 8169631633

Role & responsibilities Handle clinical and regulatory processes from application to approval for medical devices. Must have strong knowledge of the CDSCO application, review, and approval process for medical devices in India. Prepare and maintain regulatory documents, technical files, and dossiers for submissions. Support CDSCO, CE, and ISO 13485 requirements . Coordinate with internal teams for documentation, product information, and testing reports . Assist in Clinical Evaluation Reports (CER/CEE) , risk management files, and Post-Market Surveillance (PMS) reports. Ensure timely submission, follow-up, responses, and renewal of licenses and approvals. Maintain updated knowledge of EU MDR, ...

Role Overview: At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. As a Sr. Clinical Research Associate Contractor (SrCRA) at Allucent, you will independently control and monitor investigational sites, proactively detect issues, and provide solutions to ensure clinical studies are conducted according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice. Key Responsibilities: - Govern highest possible quality standards for trial monitoring activities. - Conduct all study...

We are looking for a Marketing Professional who can create high-impact marketing collateral (brochures, case studies, white papers) and lead generation efforts targeted at B2B audiences in healthcare / life-sciences / clinical research domains. The person will work closely with product, sales, and domain experts to translate technical and clinical value into marketing content that resonates with decision-makers (e.g. hospitals, CROs, pharma / biotech firms, research orgs). Key Responsibilities Marketing Collateral & Content Creation Create product brochures, white papers, data sheets, case studies, pitch decks explaining complex health-tech / AI / clinical-data solutions in clear, persuasive...

Role Overview: As the GCP Compliance Manager (GCO) at Novartis, you will be responsible for overseeing and controlling regulated GCO activities to ensure compliance with GCP standards. Your role will involve contributing to compliance activities supporting the three pillars of GCP Compliance, managing audits & inspections, and promoting a culture of product quality within GCO. Key Responsibilities: - Ensure compliance oversight and control of regulated GCO activities with a focus on activities that could impact GCO's ability to meet objectives. - Provide GxP expertise and support GCP Compliance across various functions, compliance, process, training, and risk groups. - Manage GCO wide system...

Role Overview: You will be responsible for performing monthly submissions of budgets and rolling forecasts into the financial system, with a focus on industry knowledge of Lifesciences/Healthcare. Your role will involve analysis and support activities for different departments and cost segments, as well as adhoc reporting and analysis for business stakeholders. You will lead presentations and discussions with stakeholders on analysis and adhoc requests, ensuring service quality deliverable parameters are maintained. Additionally, you will be involved in financial scenario modeling, requiring strong Excel and VBA knowledge. Your responsibilities will include ensuring timely submission of data...

Role Overview: As the Global Clinical Operations (GCO) Budget Associate Director, you will be responsible for independently providing accurate actual spend vs. endorsed budget for each assigned Clinical Trial Team (CTT) in accordance with the Operational Execution Plan (OEP) requirements. It will be your duty to maintain a realistic study level budget forecast at all times, offering a clear overview of planned monthly, quarterly, and yearly spending to the organization, including Senior Management and Finance. Additionally, you will be accountable for aligning reports with assigned OEP requirements and ensuring compliance with GCO governance, such as the Operational Excellence Board (OEB). F...

We're Nagarro, we are a Digital Product Engineering company that is scaling in a big way! We build products, services, and experiences that inspire, excite, and delight. We work at scale across all devices and digital mediums, and our people exist everywhere in the world (17700 experts across 39 countries, to be exact). Our work culture is dynamic and non-hierarchical. We are looking for great new colleagues. That is where you come in! REQUIREMENTS: Bachelors degree in Pharma, Bioinformatics, Medicine, or related disciplines. Master’s degree in Business Analytics, Engineering, or Science (preferred). 6–8 years of experience as a Business Analyst or Data Analyst within the Life Sciences domai...

Emmes Group is looking for Intern - Human Resources to join our team Roles and Responsibility Assist in recruitment processes, including scheduling interviews and maintaining candidate records. Coordinate employee onboarding and training programs to ensure a smooth transition into their new roles. Maintain accurate and up-to-date employee data and records. Support performance management systems by tracking employee progress and providing feedback. Collaborate with other departments to resolve employee-related issues and improve overall HR efficiency. Develop and implement effective HR policies and procedures to enhance organizational culture. Job Requirements Strong understanding of human re...