Study Site Activation Specialist

Are you an experienced professional with a passion for clinical research and site activation?We are seeking a highly skilled Country Study Activation Specialist to join our AbbVie team in the United States.About the Role:This is an exciting opportunity to work as a site start-up expert, providing subject matter expertise (SME) support to ensure successful...

About the RoleWe are seeking a highly skilled Study Operations Specialist to join our team at Pfizer. This role is an exciting opportunity for individuals who want to work in a dynamic environment and contribute to the success of our studies.Job DescriptionAccountable for site start-up activities through activation, including qualification and deployment of...

Job Overview: As a Site Contracts Specialist, you will be responsible for executing the feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level.Key Responsibilities:Serve as a Single Point of Contact (SPOC) to perform feasibility, site...

**Company Overview:** ICON plc is a world-leading healthcare intelligence and clinical research organization.We foster an inclusive environment driving innovation and excellence, welcoming talented individuals to join us on our mission to shape the future of clinical development.Diversity, Inclusion & Belonging: At ICON, we celebrate our diverse workforce,...

At ICON Plc, we're a world-leading healthcare intelligence and clinical research organization.We pride ourselves on fostering an inclusive environment that drives innovation and excellence. As a Senior Site Activation Lead, you'll play a vital role in helping us shape the future of clinical development.Our diverse teams enable us to become better partners to...

At ICON, our diverse teams enable us to become a better partner to our customers and help us to advance and improve patients' lives. Our company culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership, and Integrity. We want to be the Clinical...

**About This Role**Thermo Fisher Scientific has an exciting opportunity for a Site Contract Specialist to join our team. As a Site Contract Specialist, you will be responsible for preparing and negotiating contracts with study sites, as well as finalizing the contract process.Key ResponsibilitiesDrafts, reviews, negotiates and finalizes agreements with study...

About the CompanyPPD is a vital link between an idea for a new medicine and the people who need it. Our mission is to improve health by delivering life-saving therapies to patients. We are a collaborative and winning culture, striving to bend the time and cost curve of delivering clinical trials.Job DescriptionThe Site Intelligence and Activation Team...

Senior Site Activation LeadAt ICON plc, we're a world-leading healthcare intelligence and clinical research organization dedicated to fostering an inclusive environment driving innovation and excellence.We're seeking a Senior Site Activation Lead to join our team.What You'll Get:A competitive estimated salary of $120,000 per annum, based on industry...

Job DescriptionThe Senior Clinical Operations Specialist 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 client standards. This role may span over multiple...

About the RoleWe are seeking a highly skilled Site Contracts Specialist to join our team at Iqvia. This is an exciting opportunity for someone who is passionate about site activation and contract management.Key ResponsibilitiesExecute feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and...

**About the Role**Iqvia is seeking a highly skilled Clinical Research Operations Specialist to join our team. As a key member of our clinical research operations team, you will be responsible for ensuring the accuracy of data in our clinical trial management system (CTMS). You will also provide support to clinical systems end-users, conduct research and data...

Job OverviewWe are seeking a highly skilled Clinical Study Configuration Specialist to join our team at ICON plc. This is a permanent, full-time position that offers a competitive salary and a range of benefits.

Are you a seasoned professional seeking a challenging role in clinical research?We are currently looking for a Clinical Trial Activation Manager to join our dynamic team at ICON plc, a world-leading healthcare intelligence and clinical research organization.The successful candidate will be responsible for ensuring the timely activation of investigative...

Job Title: Senior Study Start Up Associate - Contracts and Budgets SpecialistAbout the Role:At ICON plc, we're passionate about advancing and improving patients' lives. As a Senior Study Start Up Associate - Contracts and Budgets Specialist, you'll play a crucial role in supporting our Study Start Up Group by reviewing and negotiating Investigator contracts...

At Johnson & Johnson Family Of Companies, we're dedicated to creating a healthier world for all. Our mission is to empower individuals and communities to live healthier, more fulfilling lives.About the RoleWe're seeking a highly skilled Clinical Trials Specialist to join our team in [Location]. This role plays a critical part in ensuring the success of our...

**Job Summary**We are seeking an experienced Senior Clinical Activation Manager to join our team at ICON. As a key member of our site activation team, you will be responsible for driving and accelerating the activation of investigator sites and implementing site activation activities for global, complex projects.**About ICON**ICON plc is a world-leading...

About ICON PlcICON Plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome talented individuals to join our mission to shape the future of clinical development.We prioritize diversity, collaboration, and partnership to become a better...

About ICONAt ICON, we provide innovative solutions for our clients in the clinical research industry. Our goal is to move drug discovery forward and help our clients develop life-saving and life-improving drugs.We are seeking a highly skilled Clinical Trial Operations Coordinator to join our team. As a key member of our operations team, you will be...

Global Study Enablement ProfessionalMilestone One, a leading Site Enabling Services organization with global headquarters in Zug, Switzerland, seeks a highly skilled Global Study Enablement Professional to support trial sites worldwide. As a key member of our team, you will play a crucial role in ensuring seamless study delivery.The ideal candidate will have...