Clinical Trials Proposal Specialist

Job SummaryWe are seeking a skilled Clinical Trial Operations Specialist to join our team at Iqvia.About the RoleThe successful candidate will be responsible for the local management of clinical trials, ensuring compliance with Sponsor SOPs, WIs, policies, codes of Good Clinical Practice (GCP), and local regulatory requirements.Key ResponsibilitiesPrepare...

Job Summary:We are seeking a highly skilled and experienced Clinical Trial Management Associate to join our team in a Senior Regional Clinical Trial Management Associate role.About the Role:As a Senior Regional Clinical Trial Management Associate, you will be responsible for supporting the Regional Clinical Study Manager in regional study delivery and...

Job DescriptionAt PSI, the Proposal Manager plays a pivotal role in the company's proposal process, ensuring a win rate of 30% and higher. This individual will contribute to all phases of proposal development, from RFP strategy to bid defense slide decks. They will collaborate with global teams of subject matter experts to rapidly produce winning...

Job Title: Regulatory Affairs SpecialistAbout the Role:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Intrials Clinical Research. As a Regulatory Affairs Specialist, you will be responsible for managing regulatory and start-up activities for clinical trials in Latin America.Key Responsibilities:- Manage regulatory and...

We are seeking a Clinical Trial Start-Up Specialist to advance clinical trial start-up activities by understanding client objectives and assisting in the development of the plan for country and site distribution.The ideal candidate will have a strong understanding of regulatory and submission processes in various countries and excellent written and verbal...

Job OverviewWe are seeking an experienced Site Network Development Specialist to join our Business Development team. This role is responsible for building and expanding the network of clients in the clinical trials industry.

Key Responsibilities:Support clients by understanding their specific requirements and providing logistical solutions.Develop and implement effective logistical strategies to meet client needs.Collaborate with cross-functional teams to ensure seamless execution of clinical trials.About the Role:This role is part of the Thermo Fisher Scientific team,...

Unlock a Career in Clinical ResearchWe are seeking a skilled and dedicated Clinical Trial Coordinator to join our team at Thermo Fisher Scientific. As a Clinical Trial Coordinator, you will play a crucial role in the success of our clinical trials, working closely with our clients to ensure timely and efficient project delivery.About the RoleThis is a...

Principal Clinical Research AssociateJob SummaryCTI Clinical Trial Services, Inc. is seeking a highly skilled and experienced Principal Clinical Research Associate to join our team. As a key member of our clinical operations team, you will be responsible for overseeing the management of clinical trials, ensuring compliance with regulatory requirements, and...

**Job Overview**The Clinical Trial Educator, based in our global network, will collaborate with trial coordinators and healthcare providers to provide information and education on clinical trial inclusion and exclusion criteria.This role requires working in partnership with CRAs and other field-based medical teams to develop tailored recruitment plans and...

About ICON plcICON plc is a world-leading healthcare intelligence and clinical research organization. We pride ourselves on fostering an inclusive environment that drives innovation and excellence.We are seeking a Clinical Trial Activation Specialist to join our dynamic team. As a key member of our team, you will be responsible for advancing clinical trial...

We are a global company that values quality and dedication, changing lives through medical science.About UsFounded in 1995, we bring together over 2000 passionate individuals to deliver exceptional results. Our team is dedicated to producing high-quality proposals that meet our clients' needs.Job DescriptionThe Proposal Manager coordinates all phases of...

**About ICON Plc**We are a world-leading healthcare intelligence and clinical research organization.Our mission is to shape the future of clinical development, and we welcome you to be a part of it.We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team.As a Clinical Trial Administrator at ICON, you will play a pivotal...

Medpace, Inc. is seeking a full-time Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo. This position plays a key role in the clinical trial management process.Key Responsibilities:Efficiently manage and successfully execute clinical trial submissions.Collaborate with cross-functional teams to ensure timely and accurate...

Key Responsibilities:As a Regulatory Submissions Manager at Medpace, you will play a vital role in the clinical trial management process. Your primary focus will be on efficiently managing and successfully completing regulatory submissions for our LATAM clinical trials.Key Skills and Qualifications:• Strong expertise in clinical trial management and...

Job SummaryIcon Plc is a leading healthcare intelligence and clinical research organization seeking a skilled Site Activation Lead to drive clinical trial start-up activities.Key ResponsibilitiesLead clinical trial start-up activities, understanding client objectives and assisting in the development of plans for country and site distribution.Oversee...

Job DescriptionWe are seeking an experienced Global Clinical Trials Manager to join our team at Allucent. As a key member of our clinical operations department, you will be responsible for providing leadership and management to the Clinical Research Associates (CRAs) and other clinical functional groups in their day-to-day clinical trial activities.Your...

Company OverviewICON plc is a global healthcare intelligence and clinical research organization dedicated to fostering innovation and excellence. Our diverse and dynamic team is committed to shaping the future of clinical development.SalaryWe offer a competitive salary of $65,000 - $85,000 per annum, commensurate with experience, in addition to a range of...

Transform your career with Tata Consultancy Services, one of the world's leading IT Services companies.About UsWe believe that people make the difference, and that's why we live a culture of unlimited learning, full of opportunities for improvement and mutual development. Join us to expand your ideas through the right tools and contribute to our success in a...

About ICON PlcICON plc is a world-leading healthcare intelligence and clinical research organization, committed to fostering an inclusive environment that drives innovation and excellence.We are currently seeking a Clinical Trial Activation Specialist to join our diverse and dynamic team. In this role, you will advance clinical trial start-up activities by...