Clinical Trial System Architect

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...

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...

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 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...

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 DescriptionThis role involves designing and developing software solutions to enable interoperability between various healthcare and clinical trial systems. The successful candidate will be responsible for ensuring compliance and streamlining data exchange between different systems. This may involve building robust APIs, data mapping, data transformation,...

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...

Job OverviewWe are a global company that provides clinical research services to the pharmaceutical, biotechnology, and medical device industries. Our mission is to advance and improve human health by accelerating the development of medicines that make a difference to people's lives.We're seeking a highly experienced Clinical Trial Manager to join our team...

About the Role:This is an exciting opportunity to join our team as a Clinical Validation Analyst and contribute to the success of our clinical programs.Key Responsibilities:Conduct data validation and quality assurance checks to ensure the integrity of clinical trial data.Collaborate with cross-functional teams to define validation requirements and develop...

About the RoleThe Senior Clinical Trial Coordinator - Biotech Healthcare will be responsible for identifying and assessing potential investigators for clinical trials, coordinating and managing regulatory and ethics committee submissions, and reviewing and ensuring accuracy of clinical study documents.Identify and assess potential investigators for clinical...

IQVIA India seeks an experienced Clinical Trial Start-up Specialist to join our team. As a Vendor Start-up Manager, you will play a critical role in ensuring the successful start-up of clinical trials.Job Description:Provide technical expertise to refine specifications and develop customized recruitment strategies.Collaborate with the Vendor Program Manager...

Key ResponsibilitiesCollaborate with IT, R&D, clinical operations, regulatory affairs, and quality assurance teams to gather and document business requirements.Translate business needs into detailed functional and non-functional specifications.Facilitate workshops and stakeholder interviews to elicit requirements.You will work on projects related to clinical...

Join Teva Pharma as a Clinical Programming ManagerAbout UsTeva Pharma is a leading manufacturer of generic medicines and a proud producer of many products on the World Health Organization's Essential Medicines List. Our mission is to make good health more affordable and accessible to millions around the world.The OpportunityWe are seeking a skilled Clinical...

Key Responsibilities- Develop and validate SDTM, ADaM datasets, and TFLs (Tables, Listings, and Figures) per regulatory and sponsor requirements.- Perform complex statistical programming for clinical trials, ensuring compliance with CDISC standards.

About the Role:This is an exciting opportunity to work as a Study Management Lead - Clinical Trials at ICON plc. As a key member of our team, you will be responsible for leading the clinical trial operations in a country, ensuring timely delivery of data to required quality as per SMA. You will also be responsible for developing and optimizing the...

Job Overview:ICON plc is seeking an experienced Clinical Trial Operations Manager to lead the clinical trial operations in a country, ensuring timely delivery of data to required quality as per SMA. The successful candidate will have excellent knowledge of international guidelines (ICH/GCP) and relevant local regulations.Main Responsibilities:Lead Local...

Job Overview: As a leading global contract research organization, Lifelancer is seeking a highly motivated and experienced Clinical Trials Site Identification Specialist to join our team. In this role, you will be responsible for developing site lists according to program or protocol requirements, collaborating with Global Feasibility Leads, and ensuring the...

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...

About the TeamIQVIA's Clinical Trial Supplies team is responsible for managing the logistics of clinical trial supplies. We are seeking an experienced Clinical Supply Coordinator to join our team. As a key member of the team, this individual will be responsible for coordinating the logistics of clinical trial supplies.Main ResponsibilitiesCoordinate supply...