Clinical Contract Specialist

Job Overview:As a Clinical Contract Specialist, you will play a crucial role in developing and implementing contracting strategies to support the delivery of clinical trials. Your expertise will be essential in negotiating contracts with sponsors, ensuring compliance with regulatory requirements, and providing high-quality contracting services to our...

Job Overview:As a Clinical Contract Specialist, you will play a crucial role in developing and implementing contracting strategies to support the delivery of clinical trials. Your expertise will be essential in negotiating contracts with sponsors, ensuring compliance with regulatory requirements, and providing high-quality contracting services to our...

Company OverviewResourcing Life Science is proud to partner with a leading Global CRO that offers a full-service solution for clinical and non-clinical development, peri-approval, and market access. Their expertise spans various pharmaceutical and biotech companies globally.Job SummaryWe are seeking a highly skilled Clinical Contract Specialist to join our...

Job OverviewIQVIA is seeking a highly skilled Clinical Trials Specialist to join our team. As a key member of our Connected Devices Solution team, you will be responsible for ensuring the smooth operation of our clinical trials.Key ResponsibilitiesValidate connected devices for clinical trials, ensuring they meet the required standards.Develop and execute...

Job OverviewIQVIA is seeking a highly skilled Clinical Trials Specialist to join our team. As a key member of our Connected Devices Solution, you will be responsible for ensuring the seamless integration of medical devices with our eSource platforms.Key ResponsibilitiesValidate Connected Devices for clinical trials, working closely with vendors and internal...

About MAI Fortrea Development Limited As a prominent global contract research organization (CRO) dedicated to scientific excellence and extensive clinical development expertise, MAI Fortrea Development Limited offers pharmaceutical, biotechnology, and medical device clients a comprehensive suite of clinical development, patient access, and technological...

About MAI Fortrea Development Limited As a prominent global contract research organization (CRO) dedicated to scientific excellence and with extensive experience in clinical development, MAI Fortrea Development Limited offers pharmaceutical, biotechnology, and medical device clients a comprehensive suite of clinical development, patient access, and...

Senior Clinical Data ManagerFortrea Drug Development is seeking a highly skilled Senior Clinical Data Manager to join our team. As a leading global contract research organization, we provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions.About the RoleThe Senior...

About MAI Fortrea Development Limited As a prominent global contract research organization (CRO) committed to scientific excellence and extensive clinical development expertise, MAI Fortrea Development Limited offers pharmaceutical, biotechnology, and medical device clients a comprehensive suite of clinical development, patient access, and technological...

Parexel Site Contract Associate Job DescriptionParexel is a leading biopharmaceutical services company that improves the world's health by transforming scientific discoveries into new treatments. We are seeking a highly skilled Site Contract Associate to join our team in Italy.Key Responsibilities:Negotiate study-specific generic and country Clinical Site...

Job Title: Sr. Clinical Research AssociateAt Allucent, we are dedicated to helping small-medium biopharmaceutical companies navigate the complex world of clinical trials. We are seeking a Sr. Clinical Research Associate to join our team.Key Responsibilities:Govern quality standards for trial monitoring activities.Perform selection, initiation, monitoring,...

JOB SUMMARY: The Clinical Site Activation Specialist plays a pivotal role in overseeing and facilitating operational tasks from initiation to conclusion for designated studies and investigator locations. This position ensures adherence to study timelines while complying with relevant regulations, Good Clinical Practices, and Pfizer's internal standards....

JOB SUMMARY: The Clinical Site Activation Specialist plays a pivotal role in overseeing and facilitating operational tasks from initiation to conclusion for designated studies and investigator locations. This position ensures adherence to study timelines while complying with relevant regulations, Good Clinical Practices, and Pfizer's internal standards....

Job DescriptionTo enable AbbVie's emergence as a world-class R&D organization, the position anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends, and communicates corrective action ensuring successful protocol-level execution of SMM deliverables involving start-up, execution, and close-out of...

Join Our Team as a Part-time Licensed Clinical Social WorkerMemory Training Centers of Florida is a rapidly growing clinical practice dedicated to optimizing the quality of life for seniors in Florida. We are seeking a part-time Licensed Clinical Social Worker to provide memory training and psychotherapy to seniors in senior living communities.Our Mission:...

Job Summary:We are seeking a highly skilled Clinical Research Associate to join our team at Thermo Fisher Scientific. As a Clinical Research Associate, you will be responsible for ensuring the integrity and quality of clinical trials.Key Responsibilities:Conduct on-site visits to monitor clinical trials and ensure compliance with regulatory...

Job Title: Senior Clinical Research AssociateAt Allucent, we are dedicated to helping small-medium biopharmaceutical companies navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.Job SummaryWe are seeking a Senior Clinical Research Associate (Sr. CRA) to join our team. As a Sr. CRA at Allucent,...

About the RoleWe are seeking a highly skilled Clinical Research Associate to join our team at Indiana Biosciences Research Institute. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials, ensuring that they are conducted in accordance with Good Clinical Practice (GCP) and regulatory requirements.Key...

JOB SUMMARY: The Clinical Trial Activation Lead is tasked with overseeing or assisting operational functions from initiation to completion for designated studies and investigator locations, ensuring adherence to study schedules and compliance with applicable regulations, Good Clinical Practices, and Pfizer's standards. Responsibilities may extend across...

Job Summary:The Clinical Site Activation Partner is responsible for leading or supporting operational activities from start-up to close-out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and Pfizer standards.Key Responsibilities:Initiate and coordinate...