Clinical Trial Programmer Manager

About the RoleWe are seeking an experienced Statistical Programmer to join our team at Biocon Biologics. In this role, you will be responsible for providing statistical input into and review of statistical deliverables, performing data manipulation, analysis, and reporting of clinical trial data, and applying SAS programming skills to create and validate...

**Overview of Clinical SAS Programmer Role**Emmes Group is seeking a skilled Clinical SAS Programmer to assist in the development of statistical programs and reports for clinical trials. The ideal candidate will have a strong background in programming languages, particularly SAS Macros, SQL, and understanding of databases.Key Responsibilities:Data cleaning,...

Clinical Trial Manager - India BangaloreICON plc is a world-leading healthcare intelligence and clinical research organization Were 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 developmentAt ICON its our people that set us apart Our diverse teams...

**Job Summary**We are seeking a Clinical Data Risk Analyst to join our team at ICON plc. As a Clinical Data Risk Analyst, you will play a key role in ensuring the integrity and quality of our clinical trial data.You will be responsible for conducting risk assessments, collaborating with cross-functional teams, and developing risk management plans and...

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 leading provider of clinical research services, we require a skilled Sr. Clinical Research Associate Contractor (SrCRA) to join our team for a...

Job OverviewWe are seeking a highly skilled Clinical Trials Specialist to join our team at Labcorp Drug Development. In this role, you will play a critical part in ensuring the accuracy and completeness of informed consent forms for clinical trials.The successful candidate will have strong analytical and troubleshooting skills, with the ability to identify...

About ICON: ICON is a leading global provider of drug development solutions and services to the pharmaceutical, biotechnology, and medical device industries. Our mission is to advance and improve patients' lives by bringing life-changing medicines to market faster and more efficiently.We are committed to fostering a diverse and inclusive culture that rewards...

Job DescriptionAs a Clinical Medical Manager, you will be part of our CMR (Clinical, Medical, Regulatory & Pharmacovigilance) team based in Bangalore, working closely with KOLs, independent professional associations, and patient advocacy associations to ensure the successful execution of clinical trials.About Our TeamWe are dedicated to driving clinical...

We are looking for an exceptional Clinical Research Scientist to join our clinical research team. As a member of our team, you will work on various clinical research projects and trials, applying your expertise in oncology, reproductive health, metabolic disorders, neurodegenerative diseases, and genomics.Key ResponsibilitiesProject Feasibility Analysis:...

About TriomicsTriomics is pioneering the development of a unified technology stack for clinical trial sites and investigators. Our mission is to make Clinical Research a seamless part of Healthcare operations. By leveraging our proprietary OncoLLM, we eliminate bottlenecks in data collection, patient recruitment, and other time-consuming tasks, enabling the...

Clinical Trials Content Manager Job DescriptionIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient...

OverviewClinical Trial AssociateLocation BangaloreICON plc is a world-leading healthcare intelligence and clinical research organisation From molecule to medicine we advance clinical research providing outsourced services to pharmaceutical biotechnology medical device and government and public health organisations With our patients at the centre of all...

Job SummaryClinical Trial Foundations is seeking a highly skilled and experienced professional to lead the development of contemporary clinical trial processes, technologies, information, and capabilities. The ideal candidate will have a strong understanding of clinical drug development, quality, and clinical information flow, with expertise in related...

About the RoleWe are seeking a Senior Clinical Program Coordinator to join our Global Medical Affairs team. As a key member of our department, you will be responsible for developing and implementing initiatives to ensure successful recruitment and retention of patients in our most important clinical trials.As a Senior Clinical Program Coordinator, you will...

Key ResponsibilitiesThe Regulatory Affairs Specialist - Clinical Trials will oversee clinical trial execution from initiation to close-out, register clinical trials on various regulatory platforms as per local regulations, and ensure timely data collection from sites for ongoing projects.Oversee clinical trial execution from initiation to close-out.Register...

Job Description:As a Software Engineer - Clinical Trials, you will be a key part of a team improving a discrete set of tools and processes into a repeatable, automated, and audited pipeline to better on-board and process data for clinical trials. This role can blend developing tools and platforms with processing large batches of data to improve transparency...

About the RoleWe are seeking an experienced Project Support Coordinator to join our team at Thermo Fisher Scientific. In this role, you will be responsible for coordinating and executing clinical trials, working closely with cross-functional teams to ensure successful trial outcomes.Responsibilities:Coordinate and oversee trial activities, ensuring timely...

Fortrea is committed to delivering high-quality clinical data to our clients. We are seeking an experienced Data Quality Expert to join our team and play a key role in ensuring the accuracy and integrity of our data. As a Data Quality Expert, you will be responsible for reviewing clinical trial data, identifying errors, and developing strategies to improve...

Job SummaryWe are seeking a highly motivated Pharmacovigilance Reporting Associate to join our dynamic team. In this role, you will be responsible for the preparation and review of safety reports related to clinical trials and post-marketing activities. You will also ensure compliance with regulatory requirements, maintain up-to-date knowledge of regulatory...

Emmes Group is a leading provider of clinical research services, committed to advancing medical discovery and improving patients' lives. Our team is dedicated to developing innovative cloud-based solutions for clinical trials, leveraging cutting-edge technologies to enhance the research process.About UsWe have over 47 years of experience in clinical...