353 Clinical Development Jobs - Page 14

Job Context: To support MIBG I-131 clinical programs and other JDI innovative products in the pipeline, The Regulatory Specialist will be reporting to the director of Regulatory Affairs and support the development of regulatory strategies related to JDI clinical programs, marketing applications in US and Canada and post-marketing activities. Challenges: 3. SCOPE and SIZE OF THE ROLE (Please indicate key metrics defining the size and scope of the role) Revenue / Operating Budget As per JDI RA budget plans Geographical Responsibilities (Global / International / Country / Area with in Country Will work with the team in Canada and based out of India Area of Impact (Dept. Location / Function or B...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Key Accountabilities : Customer Service Support service desk and direct requests from all levels of staff (including C-suite), maintain status tracking in ...

JOB DESCRIPTION Key Responsibilities: Clinical Trial Planning: Develop and execute comprehensive clinical trial plans, protocols, and study timelines in compliance with all relevant regulatory guidelines (e.g., ICH-GCP, FDA regulations). Site Management: Identify, qualify, and manage clinical trial sites and investigators. Ensure proper site initiation, monitoring, and closure. Study Oversight: Supervise all aspects of the Phase II clinical trials, including patient recruitment, data collection, and case report form (CRF) completion. Budget & Vendor Management: Manage trial budgets and timelines. Oversee and coordinate activities of contract research organizations (CROs) and other third-part...

Role & responsibilities Act as member of the multidisciplinary brand team (marketing/ Sales and internal stakeholders) Help guide the strategic direction in related therapeutic areas Apt utilization of scientific data / Medical data (identify and dissect key studies along with key messages which comply as per the UCPMP/ ethical scientific promotions) Help create convincing communication concepts in cooperation with marketing and external partners as and when needed which may be for existing products / new products Contribute to the content of promotional materials Approve promotional materials - as per the accepted scientific and ethical norms Develop good relationships with key opinion lead...

Job Title: Head Clinical Services Location: Lata Mangeshkar Hospitals, Nagpur (Hingna Campus) Organization: Lata Mangeshkar Hospitals, Nagpur Job Description: We are seeking a dynamic and experienced Head – Clinical Services to oversee and coordinate all clinical functions across Lata Mangeshkar Hospitals. The role requires a qualified medical professional with strong administrative capabilities to ensure the highest standards of patient care, compliance, and operational efficiency. Key Responsibilities: Lead and supervise all clinical departments to ensure smooth functioning and quality healthcare delivery. Develop, implement, and monitor clinical protocols, SOPs, and patient care guideline...

The Position The Statistical Monitor plays a critical role in supporting Risk-Based Monitoring within Clinical Drug Development by operating and maintaining the centralized Statistical Monitoring function. This position focuses on detecting unusual data patterns, systematic errors, and potential instances of non-compliance or fraud that may not be identified through routine monitoring processes. The Statistical Monitor analyses clinical data across trials and projects to safeguard data integrity, which is essential for the approval of new drug. The role requires a high level of independence, with the potential to mentor junior colleagues and contribute to continuous improvement in data relia...

- Successfully complete our internal training plan to include hemodynamics, ECG, angiography, echo CT imaging modalities and complete the case support and proctor delegate authorizations. - Provide active commercial case support, demonstrating excellence in procedural success rates patient outcomes. - Scrub in sterile and provide TAVI valve loading in procedures training instruction to trial and commercial customers - Provide our customers CT valve sizing analysis utilizing the Pie Medical 3Mensio CT program - Lead customer didactic education sessions for account activation before first implants - Lead pre case planning debriefing of heart team pre post procedure and provide ongoing educatio...

ZS Life Science R&D Technologist in Clinical development ZS life science R&D team partners with client to discover and develop innovative medicines that improve patient's lives. Our work spans across consulting, analytics and technology (services and platforms) projects across the several domains. We have 3500+ zs professional that are delivering R&D programs, $100MM+ invested in R&D data, analytics and technology assets and 100+ clients on R&D programs. Our Clinical/Drug Development division displays a substantial history of contributing to numerous client projects with significant results in the drug development. The Drug Development R&D Technologists possess a deep understanding of techno...

Career Category Medical Affairs Job Description Job Title: Senior Manager, Scientific Communications Role Location: Hyderabad, India About Us: Amgen harnesses the best of biology and technology to fight the world s toughest diseases, and make people s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what s known today. Role Description: The Scientific Communications Senior Manager is accountable for planning and delivering innovative scient...

Supervisor, Investigator Payments - 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 a Supervisor, Investigator Payments to join our diverse and dynamic team. As a Supervisor, Investigator Payments at ICON, you will play a key role in managing and overseeing the processing and tracking of investigator payments, ensuring timely and accurate payments in compliance with contractual and regulatory requirements. You will contrib...

Supervisor, Investigator Payments - India, Chennai - Hybrid, Office-Based We are currently seeking a Supervisor, Investigator Payments to join our diverse and dynamic team. As a Supervisor, Investigator Payments at ICON, you will play a key role in managing and overseeing the processing and tracking of investigator payments, ensuring timely and accurate payments in compliance with contractual and regulatory requirements. You will contribute to the smooth execution of clinical trials by maintaining strong relationships with investigators and sponsors while ensuring financial integrity and transparency in payment processes. What You Will Be Doing: Managing the end-to-end process of investigato...

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative one-team culture. We are looking for a dynamic person to join our in-house team as a Principal Statistical Programmer Consultant on a contract basis. Join our team: you can be part of making a difference in peoples lives and experience a fulfilling and rewarding career! Main Job Tasks and Responsibilities: Programming edit checks for Data Management with SAS. Create tables, listings and figures for clinical study report. Annotated blank CRF (acrf.pdf) following FDA/CDISC or sponsor guidelines. Create or QC SDTM specifications and SD...

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative one-team culture. We are looking for a dynamic person to join our in-house team as a Statistical Programmer Consultant on a contract basis. Join our team: you can be part of making a difference in peoples lives and experience a fulfilling and rewarding career! Main Job Tasks and Responsibilities: Programming edit checks for Data Management with SAS. Create tables, listings and figures for clinical study report. Annotated blank CRF (acrf.pdf) following FDA/CDISC or sponsor guidelines. Create or QC SDTM specifications and SDTM dataset...

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative one-team culture. We are looking for a dynamic person to join our in-house team as a Senior Statistical Programmer Consultant on a contract basis. Join our team: you can be part of making a difference in peoples lives and experience a fulfilling and rewarding career! Main Job Tasks and Responsibilities: Programming edit checks for Data Management with SAS. Create tables, listings and figures for clinical study report. Annotated blank CRF (acrf.pdf) following FDA/CDISC or sponsor guidelines. Create or QC SDTM specifications and SDTM ...

Job responsibilities Line management responsibilities including transfers, hiring, utilization, terminations, training, professional development, performance appraisals, time sheet approval, and employee counseling. Advises staff on administrative policies and procedures, technical problems, and prioritization. Assigns project work and reviews workload for all direct reports. Provides oversight and guidance on organizational goals and company objectives. Monitors quality of work and efficiency of team members with contracted scope of work and Safety Management Plan. Discusses below-target project goals with senior safety management. Manages projects where Safety and Pharmacovigilance are the...

Senior CVA, Chennai, Office based We are currently seeking a Senior Clinical Validation Analyst to join our diverse and dynamic team. As a Senior Clinical Validation Analyst at ICON Plc, you will play a key role in ensuring the accuracy and integrity of clinical trial data through rigorous validation processes. You will contribute to the success of clinical trials by implementing and overseeing validation procedures that uphold the highest standards of data quality and regulatory compliance. What You Will Be Doing: Developing and executing validation strategies and plans to ensure the accuracy and integrity of clinical trial data. Collaborating with cross-functional teams to identify validat...

Senior CVA, Chennai, 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 a Senior Clinical Validation Analyst to join our diverse and dynamic team. As a Senior Clinical Validation Analyst at ICON Plc, you will play a key role in ensuring the accuracy and integrity of clinical trial data through rigorous validation processes. You will contribute to the success of clinical trials by implementing and overseeing validation procedures that uphold the highe...

Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing projects. Plan (including organizing/preparing outlines), write (including first-draft authoring), edit, review, coordinate, and complete the regulatory documents supporting clinical development/product registration. Conduct effective document initiation meeting to ensure authoring team alignment and understanding. Build scientific-based rationale that support the purpose of more complex and/or strategic documents. Ensure data are presented in a clear, complete, accurate, and concise manner. Ensure that key data, statements and conclusi...

The Analyst role is an entry-level position within Bristol Myers Squibb s Trial Analytics, Insights, and Planning (TAIP) organization an internal consulting team dedicated to accelerating clinical development through data-driven analytics and trial planning. As an Analyst, you will be embedded in a project-based delivery team supporting a specific clinical trial. You ll work under the guidance of more senior team members to help execute feasibility analyses, forecasting models, dashboards, and other core analytics deliverables. You are not expected to be a clinical or therapeutic area expert at the start, but you will be expected to learn quickly, apply structured problem-solving, and contri...

aria-label="Job description"> Company Description About m360 Research (m360 Research is a wholly owned subsidiary of M3) : m360 Research is a full-service market research agency specializing in the healthcare space. Our proprietary panels include over 1 million physicians across 75 specialties in addition to substantial communities of allied HCPs, and payers. Founded in 2004, with a strong provenance in technology and innovation, m360 is committed to high quality and actionable insights, underpinned by robust physician verification and ISO certification (9001, 20252, 27001). International fieldwork services are complemented by full service advanced analytics to power data-driven decision mak...

Manager, Analytical Writing - Bangalore, 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 a Manager, Analytical Writing to join our diverse and dynamic team. As the Manager of Analytical Writing at ICON, you will manage a team of writers in creating high-quality, data-forward reports and documentation to support clinical research and regulatory submissions. You will collaborate with cross-functional teams to ensure that all written content is accur...

Accounts Payable Associate- Chennai 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 Job Advert Posting Summary: Responsible for ensuring timely and accurate processing, payment and reconciliation of creditor invoices, investigator payment requests and employee expense claims. What You Will Be Doing: Timely and accurate processing of AP vouchers Timely and accurate payment of AP vouchers Management of all documentation in line with statutory requirements Reconciliation of creditor acco...

Manager, Analytical Writing - Bangalore, Office-based We are currently seeking a Manager, Analytical Writing to join our diverse and dynamic team. As the Manager of Analytical Writing at ICON, you will manage a team of writers in creating high-quality, data-forward reports and documentation to support clinical research and regulatory submissions. You will collaborate with cross-functional teams to ensure that all written content is accurate, clear, and aligned with regulatory standards, helping to drive the success of clinical trials and product approvals. What You Will Be Doing: Driving and managing a team of analytical writers, providing guidance and feedback to ensure the production of hi...

Job title: Principal Biostatistician About the job Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. Build a career and you can be part of transforming our business while helping to change millions of lives. ReadyAs a Principal Biostatistician, you ll Lead or support one or several early/late phase studies, under minimum supervision of statistical team leader. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people s lives. We re also a company where you can flourish and grow your career, with countless opportunities to explore...

JOB DESCRIPTION Job Title: Clinical Data Management QA Auditor Job Location: Semicon Park About Syngene : Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and...