Oncology Clinical Trial Specialist

Are you an expert in graphic design looking to apply your skills in a fast-paced environment? Do you have a passion for creating visually appealing documents?We're seeking a highly skilled Clinical Trial Document Specialist to join our team at PSI CRO. As a specialist, you'll be responsible for designing and developing clinical trial documents that meet...

Job Title: Medical Oncology AdvisorAbout the RoleWe are seeking a highly skilled Medical Oncology Advisor to join our innovative oncology team. As a dynamic professional, you will engage with Healthcare Professionals (HCPs) to provide high-level scientific support and education.Main ResponsibilitiesScientific Support: Provide accurate and timely scientific...

Brief DescriptionThe Clinical Programmer will be responsible for the provision of data review and trial management deliverables across all compounds and trials for which these are required, and for all functional groups that require those deliverables.Essential Functions/ResponsibilitiesProgram simple to complex data review listings, exception reports,...

Job DescriptionThe Clinical Programmer will be responsible for the provision of data review and trial management deliverables across all compounds and trials.Key Responsibilities:Program data review listings, exception reports, QTL/KRIs, metrics reports, and visualizations in a fast-paced environment for clinical trial data review and management...

Job Description:We are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our Clinical Operations team in Poland, Estonia, Lithuania, or Latvia. The successful candidate will have experience in Clinical Trials and possess excellent organizational, communication, and teamwork skills.Key Responsibilities:Preparation of ISFs...

Site Name: USA - Pennsylvania - Upper Providence, Switzerland - Zug, UK - Hertfordshire - Stevenage, UK – London – New Oxford Street, USA - Massachusetts - Waltham, Warsaw Rzymowskiego 53Posted Date: Nov 21 2024Are you a pharma physician or academic clinician keen to be part of GSK's growing oncology antibody drug conjugate (ADC) portfolio for the...

Social network you want to login/join with:Clinical Trial Manager - Poland - Infectious Disease, WarsawClient:MEDPACELocation:Warsaw, PolandJob Category:OtherEU work permit required:YesJob Reference:5f717e3db534Job Views:4Posted:28.03.2025Expiry Date:12.05.2025Job Description:OverviewMedpace is a full-service clinical contract research organization (CRO). We...

Social network you want to login/join with:Field-Based Medical Advisor, Oncology (Poland/Germany), WarsawClient:TMACLocation:Warsaw, PolandJob Category:OtherEU work permit required:YesJob Reference:5cf97b7c22c5Job Views:4Posted:28.03.2025Expiry Date:12.05.2025Job Description:Field-Based Medical Advisor, Oncology (Poland/Germany)The Medical Affairs Company...

Job DescriptionWe are seeking a skilled Freelance Regional Clinical Trial Coordinator to join our team at Rho, Inc. This is a home-based opportunity in Poland, Estonia, Lithuania, or Latvia.Main Responsibilities:Preparation of ISFs (Investigator Site Files) and maintenance of TMF (Trial Master File) or the CRO Project File.Communication and guidance to CRA...

We are looking for a seasoned Oncology Field Specialist to join our team. In this role, you will develop and execute field medical affairs plans aligned with company strategies, identify and participate in key oncology congresses, and serve as an expert resource for scientific and clinical information.

About the RoleThis position is a critical component of GSK's growing oncology antibody drug conjugate (ADC) portfolio. As a Medical Director of Oncology Clinical Development, you will be responsible for leading clinical research activities, developing and executing phase 1-3 interventional clinical trials, and collaborating with medical experts to ensure...

Parexel International is seeking a Clinical Operations Assistant to support our Project Clinical Team.Responsibilities:Site Payments: Manage site payments, including processing invoices and tracking payments.Trial Master Files: Maintain accurate and up-to-date trial master files, ensuring compliance with regulations.Requirements:Qualifications: High school...

We are seeking a highly skilled Contract Analyst II to join our team!As a Contract Analyst II at ICON, you will be responsible for driving study initiation, maintaining effective communication with investigative sites and sponsors, and analysing contracts and agreements related to clinical trial activities.What You'll Do:Develop and execute plans for country...

About the RoleAs a Senior Contract Analyst at ICON, you will be responsible for managing contractual agreements, ensuring compliance, and contributing to the advancement of innovative treatments and therapies.The ideal candidate will have a strong background in contracts, negotiations, and client management, with excellent attention to detail and...

OverviewJoin us in redefining what it means to work for a CRO. Working at Rho, you'll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity's biggest challenges.At Rho, we're committed to you just as you're committed to us. You'll have the opportunity to...

OverviewJoin us in redefining what it means to work for a CRO. Working at Rho, you'll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity's biggest challenges.At Rho, we're committed to you just as you're committed to us. You'll have the opportunity to...

Freelance Regional Clinical Trial Coordinator Job SummaryThis is a home-based opportunity in Poland, Estonia, Lithuania, or Latvia. The successful candidate will have excellent communication and organizational skills and be able to work independently.Main Responsibilities:Preparation of ISFs and maintenance of TMF or CRO Project File.Communication and...

We are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our Clinical Operations team in Poland, Estonia, Lithuania, or Latvia. The successful candidate will have experience in Clinical Trials and possess excellent organizational, communication, and teamwork skills.Key Responsibilities:Preparation of ISFs (Investigator Site...

Clinical Research is a vital part of ICON's mission to shape the future of clinical development. As a Clinical Research Coordinator, you will be responsible for supporting Investigator Site staff in conducting clinical research studies according to project-specific requirements and regulatory guidelines.Key responsibilities include assisting in study-related...

ICON is committed to delivering high-quality clinical research services, and we are seeking a skilled and motivated individual to join our team as a Clinical Research Coordinator. In this role, you will be responsible for supporting the day-to-day activities of clinical research studies conducted at Investigator Sites.Key responsibilities include assisting...