Clinical Trials Contract Specialist

{"title": "SSU & Regulatory Specialist with Experience in Clinical Trials", "subtitle": "Join Syneos Health", "content": "**About Us**Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern...

Job SummarySyneos Health, Inc. is seeking a highly skilled Site Contracts Specialist to join our team. As a key member of our clinical trials team, you will be responsible for administering all contract management processes, including coordination with relevant protocol, informed consent, institution, investigator, vendor, consultant, and customer agreement...

Job Summary:We are seeking a highly skilled Clinical Trials Due Diligence Specialist to join our team at Syneos Health Clinical. As a key member of our team, you will be responsible for applying your technical expertise to complete and record assigned due diligence tasks.Key Responsibilities:Conduct thorough due diligence reviews of clinical trials and...

Job SummaryAs a Senior Clinical Operations Specialist at Syneos Health Clinical, you will play a critical role in ensuring the successful execution of clinical trials. This position requires a strong understanding of clinical trial operations, regulatory compliance, and data management.Key ResponsibilitiesAttend Trusted Process meetings as a subject matter...

About the RoleWe are seeking a highly skilled and detail-oriented Associate I, TMF Operations Specialist to join our team at Worldwide Clinical Trials. As a key member of our operations team, you will play a critical role in ensuring the quality and integrity of our clinical trial documents.Key ResponsibilitiesProcess Trial Master File (TMF) documents for...

Job SummaryWe are seeking a highly skilled and experienced Clinical Trials Manager to join our team at Amgen. As a key member of our clinical operations team, you will be responsible for leading and managing the conduct of clinical trials from study start-up to close out at a country level.Key ResponsibilitiesPartner with global and local country teams to...

Job SummaryWe are seeking a highly skilled and experienced Senior Clinical Trials Assistant to join our team at IQVIA. As a key member of our clinical research team, you will be responsible for leading and overseeing the execution of clinical projects and research studies in accordance with global and local regulations.Key ResponsibilitiesProvide...

Job Title: Clinical Specialist IcAt Boston Scientific Corporation, we are seeking a highly skilled Clinical Specialist Ic to join our team. As a Clinical Specialist Ic, you will play a key role in the success of our clinical trials and product development.Key Responsibilities:Assist in the site selection, qualification, and initiation processes for trialsKey...

About the RoleWe are seeking a highly skilled Clinical Specialist to join our team at Boston Scientific Corporation. As a Clinical Specialist, you will play a critical role in supporting the clinical trials process, ensuring compliance with regulatory and company guidelines, and providing training and education to physicians and hospital staff.Key...

About the RoleWe are seeking a highly skilled Contract Analyst II to join our team at ICON plc, a world-leading healthcare intelligence and clinical research organization. As a Contract Analyst II, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative...

Job SummaryWe are seeking a highly skilled Clinical Trial Manager to join our team at Icon. As a Clinical Trial Manager, you will be responsible for overseeing the planning, execution, and monitoring of clinical trials.Key ResponsibilitiesDevelop and implement clinical trial protocols and proceduresCollaborate with cross-functional teams to ensure trial...

{"title": "Clinical Research Feasibility Specialist", "content": "Join EtCurae's Team as a Clinical Research Feasibility SpecialistEtCurae is a leading clinical research organization dedicated to saving lives through the development of safer and more effective medicines. We are seeking a highly skilled Clinical Research Feasibility Specialist to join our...

Clinical Trials Quality Assurance AuditorAt PSI Cro, we are seeking a highly skilled Quality Assurance Auditor to join our international team. As a Quality Assurance Auditor, you will play a critical role in ensuring the high quality of our clinical trials and internal company processes.Key Responsibilities:Prepare, conduct, and report on QA study audits,...

About Syneos HealthAt Syneos Health, we are a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of...

About the RoleAt ICON plc, we're seeking a highly skilled Contract Analyst II to join our dynamic team. As a key member of our organization, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Key ResponsibilitiesReview and...

Transform Clinical Development with FortreaAs a leading global contract research organization (CRO), Fortrea is seeking a skilled Clinical Document Specialist to join our global Clinical Pharmacology Services team. This role offers a unique opportunity to work in a fast-paced environment, collaborating with project management and phase I monitoring teams to...

About the RoleWe are seeking a highly skilled Clinical Study Manager II to join our team at ICON. As a Clinical Study Manager II, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Key ResponsibilitiesLead the planning,...

Job SummaryWe are seeking a highly skilled and experienced Site Manager to join our team at Johnson & Johnson. As a Site Manager, you will be responsible for ensuring the smooth execution of clinical trials at our investigative sites.Key ResponsibilitiesSite Management: Serve as the primary contact point between the Sponsor and the Investigational Site,...

About the RoleWe are seeking a highly organized and detail-oriented Associate II, TMF Operations to join our team at Worldwide Clinical Trials. As a key member of our operations team, you will be responsible for the processing, maintaining, and archiving of essential documents in compliance with relevant Standard Operating Procedures, ALCOA principles,...

About the RoleAt ICON Plc, we're committed to advancing and improving patients' lives through our work in clinical research. As a Clinical Trial Manager, you'll play a critical role in delivering high-quality clinical trials that meet our clients' needs.Key Responsibilities:Oversee the clinical aspects of studies, ensuring timely and efficient...