Senior Clinical Trial Recruiter

Clinical Trial Management ProfessionalWe are looking for a highly experienced Clinical Trial Management Professional to join our team at Innovaderm Research Inc. As a key member of our clinical trials group, you will be responsible for leading multiple projects simultaneously and ensuring timely delivery of high-quality results.Key ResponsibilitiesDevelop...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

There's one thing you do that's exceptional: lead. You formulate a plan and empower your team to provide clinical expertise to health care providers helping them to improve patient outcomes. Your capacity to creatively strategize, motivate clinicians, and elicit achievement makes you the right fit for a Field Director role with Syneos Health. ...

Job Title: Supply & Logistics LeadLocation: [Location not specified]About Us: Globallogic is a leading provider of clinical trial supply and logistics services. Our team of experts works closely with clients to deliver high-quality projects on time and within budget.Job Summary:We are seeking an experienced Supply & Logistics Lead to join our team. The...

Job OverviewXepelin prioritizes people first and strives to make a positive impact on the world.We are committed to discovering and bringing life-changing medicines to those who need them.The Clinical Research Lead is responsible for managing clinical Investigators and sites participating in Lilly clinical trials and Post Marketing Safety Studies.This role...

Xepelin is committed to delivering high-quality clinical research programs that transform lives. As a Clinical Research Lead, you will play a critical role in ensuring the success of our trials by managing clinical investigators and sites.Your primary responsibilities will include:Site identification and qualificationTimely delivery of clinical trial...

About the RoleThis exciting opportunity is for a Clinical Trial Coordinator - Regulatory Expertise to join our dynamic team. The successful candidate will work closely with cross-functional teams to ensure regulatory compliance and contribute to the development of innovative biopharmaceutical solutions.ResponsibilitiesAssist in the identification and...

Lilly is a global healthcare leader that unites caring with discovery to make life better for people around the world. Our employees work together to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.We're looking for a...

We are a dynamic, global company founded in 1995, bringing together over 2,700 driven, dedicated and passionate individuals.Our team works on the frontline of medical science, changing lives and bringing new medicines to those who need them.In this role, you will provide direct operational support to project teams, ensuring that PSI clinical projects start...

About the RoleLilly is a global healthcare leader that unites caring with discovery to make life better for people around the world.Our employees work together to discover and bring life-changing medicines to those who need them, improve disease understanding and management, and give back to our communities through philanthropy and volunteerism.We prioritize...

The Global Patients and Site Solutions division of IQVIA houses a global recruitment, marketing, and site optimization team with approximately 150 staff. This team specializes in engaging and communicating with patients and clinical sites on various healthcare topics.As a Senior Patient Recruitment Lead, you will play a key role in strategic operations and...

Career OpportunityThis is an exceptional chance to work as a Clinical Trial Associate in our pharmacovigilance team at IQVIA Argentina. You will be responsible for reviewing, analyzing, and processing safety data from various sources, ensuring compliance with applicable regulations and guidelines.Main ResponsibilitiesAnalyze and process safety data according...

About the Role:This Trial Master File Coordinator position is an exciting opportunity for a detail-oriented individual to support the clinical research team in delivering high-quality Trial Master Files. The successful candidate will have a strong background in life sciences, excellent communication skills, and the ability to work collaboratively in a...

Job DescriptionThe Trial Operations Coordinator role at IQVIA Argentina involves working closely with cross-functional teams to deliver clinical studies. The successful candidate will have experience in project coordination and a strong understanding of clinical trial conduct.Responsibilities:Achieve project quality by identifying quality risks and issues,...

Job OverviewA Clinical Trial Assistant provides administrative support to the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery. Key responsibilities include:Assisting CRAs and RSU team with updating and maintaining clinical documents and systems.Preparing, handling, distributing,...

About the RoleThe Country Trial Management Specialist will play a critical role in planning, start-up, and management of clinical trials within a defined country or region.Key AccountabilitiesAct as the subject matter expert for country or regional clinical trial operationsSupport country or regional corporate operations functions as necessary (human...

About the Role: We are seeking a highly motivated and organized individual to oversee the activation of clinical trial sites in Argentina. The ideal candidate will have excellent communication and project management skills, with a strong understanding of ICH GCP and local regulations.Key Responsibilities:Coordinate site identification and selection...

**Job Overview**We are seeking a highly skilled and experienced SAS Programmer to join our global Data Management team at Psi Cro. As a key member of the team, you will be responsible for delivering high-quality clinical databases and ensuring the accuracy and consistency of clinical data.Key Responsibilities:Act as a primary point of contact for data...

Job SummaryThe Senior Clinical Research Associate will play a pivotal role in the planning, execution, and management of clinical trials. This position requires an experienced professional who can ensure the integrity of clinical data, compliance with regulatory requirements, and the overall success of clinical research projects.Key ResponsibilitiesPerform...