Study Start-Up Specialist

About the JobThis Study Site Management Lead position involves overseeing the entire site start-up process, from feasibility assessment to site closure. The ideal candidate will have strong presentation, documentation, and interpersonal skills, with the ability to handle multiple tasks to meet deadlines and deliver high-quality work in a dynamic...

Job DescriptionThe Principal Country & Site Activation Manager (Global Start Up Study Manager) plays a critical role in the success of our clinical trials. This position is responsible for overseeing the country and site activation process, ensuring that all necessary steps are taken to activate sites and start trials on time. This includes developing and...

Company DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services...

Responsibilities:The Site Activation Manager will oversee site selection and study start-up activities, ensuring operational efficiency and alignment with study timelines and financial goals.Main Tasks:Manage site selection and study start-up teams to achieve operational excellenceEvaluate teams' performance and provide feedback to improve their...

Study Start Up Associate - Bucharest, Romania - office or homebasedICON 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 you to join us on our mission to shape the future of clinical development.We are currently seeking a...

Study Start Up Associate II - Warsaw, Poland - office or homebasedICON 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 you to join us on our mission to shape the future of clinical development.As a member of the Study Start Up...

ResponsibilitiesDrive study initiation by reviewing and negotiating clinical site investigator contracts and budgetsMaintain communication with investigative sites, sponsors, and internal personnel regarding contract status and related documentsAnalyze and review contracts, agreements, and legal documents related to clinical trial activities and vendor...

Join to apply for the Associate Director, Start Up (Poland) role at Tomasz Rutkowski Solo Law Firm.The Associate Director, Start-Up is responsible for activities related to site selection, site budget and contracting, and other tasks related to the activation of clinical trial sites. The position requires the incumbent to contribute subject matter knowledge...

Job Description:As a Study Start Up Associate at ICON, you will play a pivotal role in facilitating the initiation of clinical trials. You will ensure compliance with regulatory requirements and contribute to the advancement of innovative treatments and therapies.Assist in the preparation and submission of regulatory documents, such as clinical trial...

About the RoleThe Country Study Start Up Specialist will be responsible for driving and executing all start-up and maintenance related activities and deliverables for assigned studies and sites in their designated country or countries.This role requires a proactive approach to ensure successful and on-time execution of start-up and maintenance activities, as...

The Associate Director, Start-Up is responsible for activities related to site selection, site budget and contracting, and other tasks related to the activation of clinical trial sites. The position requires the incumbent to contribute subject matter knowledge to support strategic expansions, process improvements, and decision making within the organization....

Social network you want to login/join with:Study Start-Up Site Manager with French language (prior experience needed), WarsawClient: IQVIALocation: Warsaw, PolandJob Category: OtherEU work permit required: YesJob Reference: 4d47033ee6a0Job Views: 5Posted: 15.03.2025Expiry Date: 29.04.2025Job Description:Real-World EvidenceEMEA basedJoin us on our exciting...

About the RoleThe Study Site Management Lead will play a critical role in the site start-up process, ensuring that all necessary steps are taken to prepare the site for a study. This includes conducting feasibility assessments, identifying potential sites, and coordinating with site staff to ensure a smooth start-up process.ResponsibilitiesConduct...

Study Support Specialist Job DescriptionWe are seeking a highly skilled Study Support Specialist to join our team and contribute to the success of our clinical research studies.Supports Investigator Site staff in conducting clinical research studies according to project-specific requirements and regulatory guidelinesCoordinates and executes monitoring visits...

About the RoleThe Global Trial Coordinator is responsible for managing study execution from start-up through close-out, ensuring timely and quality delivery. This role requires strong organizational and problem-solving skills, as well as excellent communication and interpersonal skills.Key Responsibilities:Coordinate study team activities, including...

About the RoleWe are seeking an experienced Study Site Management Lead to join our team. In this role, you will be responsible for conducting end-to-end site start-up from feasibility to site closure. You will serve as the primary point of contact for the site, country, and study team, coordinating site identification at a country and regional level,...

Parexel FSP offers you the security of a long-term position and many opportunities for career progression.We are currently recruiting talented and passionate people to join our FSP teams in Poland.The Clinical Study Administrator position is flexible office-based in Warsaw and gives you the opportunity to join a team with a wide range of experience and...

Job SummaryUnder the guidance of the Study Site Management leadership, this position will be responsible for conducting end-to-end site start-up from feasibility to site closure serving as the primary point of contact for the site, country, and the study team. This includes supporting site level feasibility assessments, coordinating site identification at a...

Job SummaryUnder the guidance of the Study Site Management leadership, this position will be responsible for conducting end-to-end site start-up from feasibility to site closure serving as the primary point of contact for the site, country and the study team. This includes supporting site level feasibility assessments, coordinating site identification at a...

We are looking for a highly skilled and detail-oriented individual to fill the position of Clinical Trial Assistant at ICON Strategic Solutions. This role involves providing support to Site Managers and coordinating various aspects of clinical trials.Key Responsibilities:Collaborate with Site Managers: Work closely with Site Managers to distribute and track...