Clinical trials project specialist

Job SummaryThe Clinical Trials Project Specialist will be responsible for planning and executing clinical studies in support of corporate objectives. The ideal candidate will have a strong understanding of clinical study development and execution, with excellent analytical, organizational, and communication skills.Main Responsibilities• Oversee the...

Clinical Trials Translation Specialist WantedWe are seeking a skilled Clinical Trials Translation Specialist to join our team at ProZ. The ideal candidate will have experience in translating clinical trial documents, including protocols, investigator's brochures, informed consent forms, and chemistry and manufacturing controls.Key Responsibilities:Translate...

Clinical Trial Project Lead Role SummaryAs a Clinical Trial Project Lead at INSTITUT D'EXPERTISE CLINIQUE SINGAPORE PTE LTD, you will oversee clinical trial projects from initiation to completion, ensuring all phases are executed efficiently and effectively. Key responsibilities include handling various administrative tasks to support project activities...

Clinical Trials Monitoring Manager RoleThis position is responsible for designing, planning, and conducting clinical research trials by effectively coordinating the activities of study coordinators and investigators and ensuring compliance with study protocols, FDA and International regulations, IRB and/or Ethics committees requirements, and overall clinical...

Roles & ResponsibilitiesWe are looking for a Manager with sufficient professional experience and stature to fulfill a specialist role that can contribute to the development of the clinical trial program within National Cancer Centre Singapore. The role will mainly assist our Clinical Trials Office to review and finalize contracts related to clinical trials...

We are seeking an experienced Clinical Trials translator to work on our projects in Singapore. As a key member of our team, you will be responsible for translating clinical trial documents from English to Brazilian Portuguese.Job Description:We are looking for qualified translators with expertise in the pharmaceutical industry, particularly in Clinical...

Roles & ResponsibilitiesAs a Clinical Trials Monitoring Manager, you will design, plan and conduct clinical research trials by effectively coordinating the activities of study coordinators and investigators. This role ensures compliance with study protocols, FDA and International regulations, IRB and/or Ethics committees requirements, and overall clinical...

Clinical Trials Associate Apply locations Singapore time type Full time posted on Posted Yesterday job requisition id R1452762 This is a unique opportunity for you to embark on your career in the clinical trial world and be trained by professionals from IQVIA. In this role, you will be involved in the process of supporting clinical trials for various...

Roles & ResponsibilitiesJob Overview:We are seeking a highly motivated and detail-oriented Clinical Trial Assistant to join our team. The Clinical Trial Assistant will serve as the unblinded point of contact for logistics vendors and unblinded Clinical Research Associates (CRAs), responsible for managing various aspects of clinical trial logistics and...

Medpace is a leading full-service clinical contract research organization (CRO) dedicated to accelerating the global development of safe and effective medical therapeutics. With over 5,000 employees across 40+ countries, we provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.We are committed to...

Looking for a skilled Clinical Trials translator to join our team.Job posted at: Singapore (GMT).Job type: Translation/editing/proofing jobServices required: Translation, Checking/editingLanguages: English to PortugueseJob description: We are seeking qualified English to Brazilian Portuguese freelancers/vendors for our Clinical Trials related projects....

Roles & ResponsibilitiesResponsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager; Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports within the clinical trial management system; ...

Clinical Trials Translation Project in PortugueseProZ is seeking a qualified translator to work on a Clinical Trials project in Brazilian Portuguese. The project involves translating various documents, including protocols, investigator's brochures, informed consent forms, and chemistry and manufacturing controls.RequirementsExperience in translating Clinical...

Clinical Trials Translation ProjectWe are seeking skilled Spanish translators to work on our Clinical Trials related Projects. The ideal candidate will have experience in translating clinical documents, such as protocols, investigator's brochures, and informed consent forms.Project Details:Translation of clinical documents, including protocols,...

About the OpportunityWe are seeking a highly skilled localization expert to work on our Clinical Trials related Projects. This is an exciting opportunity for experienced professionals to collaborate with our team and contribute their expertise in English to Bulgarian translation, editing, and proofreading.Key ResponsibilitiesTranslation of clinical...

Job Summary Medpace is currently looking for Clinical Trial Manager (CTM) to lead global clinical research studies. This position is fully office-based in our Singapore office. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials....

Clinical Trials Translation and Editing ProjectWe are seeking experienced Taiwanese freelancers to work on our Clinical Trials related projects. The ideal candidate will have a strong background in translation, editing, and proofreading, with a focus on clinical trials documents.Project Details:ProtocolInvestigator's Brochure (IB)Informed Consent Form...

Clinical Trials Translation Services RequiredWe are seeking a qualified English to Traditional Chinese translator for our Clinical Trials projects. The ideal candidate will have a strong background in pharmacy, medicine, biology, or biomedicine and experience in translating CMC and clinical documents.Key Responsibilities:Translate protocol, investigator's...

Project Overview:We are seeking a skilled English to Japanese freelance translator for our clinical trials related projects in Singapore.About the Project:The ideal candidate will have experience in translating and editing clinical documents, such as protocols, investigator's brochures, informed consent forms, and chemistry and manufacturing...

Roles & ResponsibilitiesThe Clinical Research Coordinator (CRC) shall help investigators conduct mainly investigator-initiated clinical trials. The CRC has to ensure that clinical trials are conducted and recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory requirements and the Clinical Trials...