3474 Clinical Trials Jobs - Page 29

Job Description Clinical Operations Program Manager Single Sponsor (Novartis) Are you a clinical operations professional with a passion for feasibility and strategic planning in global trials? We are seeking a Clinical Operations Program Manager (Global Feasibility Lead) to join our Single Sponsor Department , dedicated exclusively to Novartis . In this role, you will lead early viability, feasibility, allocation, and site selection activities to support global clinical development programs. What We re Looking For To thrive in this role, you should bring: 4 5 years of global feasibility experience in clinical trials Strong analytical and strategic planning skills , including scenario plannin...

We are seeking a candidate with knowledge of clinical trials and the end-to-end management of biospecimens. You will be an independent contributor who will work closely with our Clinical Teams to develop and implement biospecimen management plan for BMS-sponsored Phase 1-4 clinical trials. Critical to this role is the ability to oversee timelines for specimen data delivery and thereby, enabling quick decision-making and ensuring BMS s continuous competitive advantage. Key Responsibilities Oversee and manage the complete lifecycle of biospecimens collected for clinical studies with minimal supervision. Clinical Team member responsible for providing shipping/sample movement and management incl...

Let s build the future of medicine together. Join Enveda as a Manager, Engineering in Hyderabad and help us transform natural compounds into life-changing medicines. we're a team driven by curiosity and innovation are you'ready to make a difference On-Site | Hyderabad, India | Full-Time | What Makes Us Enveda Life is smart, and we can learn from it. we're reinventing drug discovery by harnessing nature s intelligence. Our platform identifies new medicines four times faster than the industry standard because patients can t wait. What sets Enveda apart isn t just what we'do it s how we'do it. Our culture is built on creativity, collaboration, and deep respect for each other. We believe People ...

Develop and implement advanced statistical models, decision support models and optimization techniques to solve complex business problems Collaborate with cross-functional teams to gather/analyze data, define problem statements and identify KPIs for decision-making Apply statistical analysis, regression modeling, clustering, segmentation, etc. to uncover trends and drivers in the data Conduct portfolio analyses to optimize resource allocation, product positioning and investment strategies Design & implement test designs to evaluate effectiveness of marketing campaigns, pricing strategies or other business initiatives Develop measurement frameworks and KPI dashboards to monitor business perfo...

Position Summary: The Clinical Research Associate (CRA) is a primary point of contact at the site level for both internal and external stakeholders, responsible for overseeing the quality, integrity and compliance of clinical trial sites in accordance with the protocol, Standard Operating Procedures (SOPs), International Council for Harmonization (ICH) Guideline for Good Clinical Practice (GCP), and applicable regulatory requirements. Duties/Responsibilities: Conduct site qualification, initiation, routine monitoring and close-out visits across all trial phases in accordance with the Site Monitoring Plan, ensuring adherence to protocol, BMS Standard Operating Procedures (SOPs) and ICH GCP Ma...

Let s build the future of medicine together. Join Enveda as a Manager, Engineering in Hyderabad and help us transform natural compounds into life-changing medicines. We re a team driven by curiosity and innovation are you ready to make a difference? On-Site | Hyderabad, India | Full-Time | What Makes Us Enveda Life is smart, and we can learn from it. We re reinventing drug discovery by harnessing nature s intelligence. Our platform identifies new medicines four times faster than the industry standard because patients can t wait. What sets Enveda apart isn t just what we do it s how we do it. Our culture is built on creativity, collaboration, and deep respect for each other. We believe People...

Functional Area Description The Senior Clinical Scientist reports through the Clinical Science function which provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective Responsible for implementation, planning, and execution of assigned clinical trial activities. Serves as Clinical Trial Lead for one or more trials Successfully leads, plans, and executes trial level activities for multiple trials with minimal to moderate level of supervision Provides scientific and clinical leadership to team of supporting Clinical Scientists (matrix leadership) Co-Leads study team meetings in partnership with GDO protocol manager; and collaborat...

Work closely with key stakeholders and RDQ pillars to understand their innovation needs and propose effective solutions leveraging advanced analytics and Gen AI/Machine Learning solutions to enable process optimization and data-driven decision making. Proactively identify areas for innovation and analytic solutions and create and execute strategies to plan and deliver the capabilities. Continuously assess the external landscape and stay informed about industry practices and new developments, proposing fit-for-purpose solutions to support, enhance, and optimize R&D Quality processes. Champion a digital first mindset and culture of Innovation. Attend and present at industry conferences to repr...

Responsible for implementation, planning, and execution of assigned clinical trial activities in Early Clinical Development Successfully leads, plans, and executes trial level activities for multiple trials with minimal to moderate level of supervision. Serves as a primary source of medical accountability and oversight for multiple clinical trials. Provides clinical, medical and scientific expertise to cross-functional BMS colleagues Duties/Responsibilities Participates in designing and developing clinical studies and research plans in support of asset strategy with the Early Clinical Development Leadership team; clinical studies include first-in-human Phase I, proof of concept Phase I/II, e...

Candidate should be B.Pharm Candidate should have regulatory exposure/ in previous organisation Candidate should have well command on IPQA activities Candidate should have Command on packaging operations Candidate should be able to work in shift well aware with regulatory requirement

We are seeking a Senior Cybersecurity Engineer for our Web Application Firewall (WAF) team. In this role, you will be responsible for supporting and optimizing the BMS Web Application Firewall capabilities, ensuring the highest level of protection for our critical business applications. You will be a crucial player in our security operations, bringing expertise in WAF technologies and delivering innovative solutions. Key Responsibilities: Provide expert support for the Imperva Cloud Web Application Firewall (CWAF) platform. Oversee onboarding, proactive monitoring, configuration, and integration of CWAF for BMS s mission-critical applications. Act as a trusted cybersecurity advisor, deliveri...

We are currently seeking a Clinical Data Coordinator I to join our diverse and dynamic team. As a Clinical Data Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies. What you will be doing Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures. Review clinical and third-party data based on edit specifications and data review plans. Issue clear, accurate, and concise queries to investigational sites. As required, communicate effectively with peers, clinical data scientist and funct...

Experienced professional individual contributor that works under limited supervision. Applies subject matter knowledge in the area of Medical Affairs. Requires capacity to apply skills/knowledge within the context of specific needs or requirements. Main Responsibilities As the Experienced professional in the Medical Affairs Sub-Function, possesses we'll developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities. Contributes to implementation of clinical protocols, and facilitates completion of final reports. Recruits clinical investigators and negotiates study design and costs. Responsible for directing human clinical trials...

Experienced professional individual contributor that works under limited supervision. Applies subject matter knowledge in the area of Medical Affairs. Requires capacity to apply skills/knowledge within the context of specific needs or requirements. MAIN RESPONSIBILITIES As the Experienced professional in the Medical Affairs Sub-Function, possesses we'll developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities. Contributes to implementation of clinical protocols, and facilitates completion of final reports. Recruits clinical investigators and negotiates study design and costs. Responsible for directing human clinical trials...

Clario Imaging is looking for a detail-oriented and proactive Automation Analyst to join our innovative team dedicated to advancing clinical trial technologies. In this role, you will be instrumental in building and maintaining robust automated testing frameworks that ensure the precision, reliability, and regulatory compliance of our software solutions. You will collaborate closely with cross-functional teams to drive quality assurance initiatives, leveraging your expertise in Selenium, Java, and Katalon Studio to streamline testing processes and enhance product performance. What We Offer Competitive compensation, incentives and shift allowances Attractive Benefits (Provident Fund, Medical ...

Job Title: Medical Writer Business Unit: Clinical Research Location: Sun House, Mumbai 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 together and support each other s journeys. Key responsibilities: Develop and update process documents, SOPs and trackers for Medical...

Hi , We are hiring for Leading ITES Company for SDTM Programmer Profile. To Apply, WhatsApp 'Hi' @ 9151555419 Follow the Steps Below: >Click on Start option to Apply and fill the details >Select the location as Other ( to get multiple location option ) a) To Apply for above Job Role ( Mumbai ) Type : Job Code # 208 b) To Apply for above Job Role ( Pune ) Type : Job Code # 209 Key Skills : Looking for an SDTM programmer with Min 3 + years experience in SDTM programming and SAS programming Should have good knowledge of CDISC standards, Trial Design domains, Define Qualifications - Health Care Professional OR Masters/Bachelor’s degree in Life Sciences/Physician Please go through the JD and we w...

Job Description Main Purpose of the Role Summarize the main purpose of the role Experienced professional individual contributor that works under limited supervision. Applies subject matter knowledge in the area of Medical Affairs. Requires capacity to apply skills/knowledge within the context of specific needs or requirements. Main Responsibilities List the main responsibilities this role regularly performs. As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities. Contributes to implementation of clinical protocols, and facilitates complet...

Role & responsibilities Literature review, feasibility evaluation and study design for Bioequivalence studies Thorough understanding of national and international regulatory guidance on Bioequivalence Review of clinical study documents of Bioequivalence studies in healthy subjects and patient PK study Clinical study monitoring Knowledge of IPs management Preparation and maintenance of Trial master file Oversee the overall management of Bioequivalence studies Basic understanding of project contract with service providers Ready to take up any other relevant tasks as and when needed

We are seeking a highly motivated and detail-oriented Research Ops Intern- Clinical Data to join our dynamic team. The ideal candidate will have a strong background in oncology, the ability to understand and interpret medical terminology from Electronic Health Records (EHR) and medical reports, and the expertise to extract and analyze data from patient notes. The candidate must have a background of clinical research and is able to comprehend clinical trials. Also have good knowledge about patient pre-screening, enrolling participants in oncology clinical trials . The role requires proficiency in Google Sheets and Excel, along with the ability to correlate medical data to meet specific requir...

Minimum 7+ years of experience as a Business Analyst & E2E Requirement Gathering(BRD,FRD,FSD). Experience in the Pharma domain would be an added advantage & Quality guidelines and regulations for "Good Practices(GXP,GMP,GLP Ectc.) Create functional specifications as user stories in JIRA to support an Agile development process using CICD Pipeline Collaborate with the Technical Analyst and development team to ensure understanding of specifications Identify, assess, and document business requirements, recommend business priorities, and advise on options and risks and changes. Act as the subject matter expert, providing in-depth systems expertise from a functional perspective in a support capaci...

Conduct in-depth research on target accounts, including decision-makers, challenges, and opportunities Analyze industry trends in clinical trials, real-world evidence, and digital health technologies Perform competitive intelligence research to inform our marketing and product strategies Develop and maintain a knowledge base of market insights for use across the companies Stay updated on regulatory changes and their potential impact on Maxis Group s services Prepare comprehensive reports and presentations for leadership, BD and marketing teams Assist scientific content writer to develop charts and graphs and informational and insights driven data for pitching and collateral purpose Requireme...

Job Title: Medical Writer Business Unit: Clinical Research Location: Sun House, Mumbai 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 together’ and support each other’s journeys.” Key responsibilities: Develop and update process documents, SOPs and trackers ...

About The Role Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy/Bachelor in Physiotherapy/Bachelor Degree in Life Sciences Years of Experience: 1 to 3 years Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on ...

About The Role Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate Qualifications: Bachelor of Pharmacy/Bachelor Degree in Life Sciences Years of Experience: 0 to 1 years Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technol...