Current jobs related to Clinical Trial Coordinator - Reading - Pharmiweb

  • Clinical Trial Coordinator

    1 month ago

    Reading, Reading, United Kingdom Verbatim Pharma Full time

    Join Verbatim Pharma as a Clinical Trial CoordinatorWe are working with a global company based in Reading, a global service partner for pharmaceutical and biotech firms, specialising in clinical trial services.The company has a great company culture that is a friendly, energetic and a multi-cultural. The company is home to employees from various backgrounds...

  • Clinical Trial Coordinator

    1 month ago

    Reading, Reading, United Kingdom Verbatim Pharma Full time

    Join Verbatim Pharma as a Clinical Trial CoordinatorWe are working with a global company based in Reading, a global service partner for pharmaceutical and biotech firms, specialising in clinical trial services.The company has a great company culture that is a friendly, energetic and a multi-cultural. The company is home to employees from various backgrounds...

  • Clinical Trial Supply Coordinator

    3 weeks ago

    Reading, Reading, United Kingdom Verbatim Pharma Full time

    Job DescriptionVerbatim Pharma is collaborating with a global company based in Reading to find a skilled professional for a clinical trial supply role.The company is a global service partner for pharmaceutical and biotech firms, specializing in clinical trial services. They have a dynamic company culture that values diversity and inclusivity.This role will...

  • Clinical Trial Supply Coordinator

    3 weeks ago

    Reading, Reading, United Kingdom Verbatim Pharma Full time

    Job DescriptionVerbatim Pharma is collaborating with a global company based in Reading to find a skilled professional for a clinical trial supply role.The company is a global service partner for pharmaceutical and biotech firms, specializing in clinical trial services. They have a dynamic company culture that values diversity and inclusivity.This role will...

  • Clinical Trials Coordinator

    3 weeks ago

    Reading, Reading, United Kingdom Pharmiweb Full time

    Clinical Trials Assistant Job DescriptionAt Pharmiweb, we are seeking a highly organized and detail-oriented Clinical Trials Assistant to join our team. As a Clinical Trials Assistant, you will play a crucial role in ensuring the smooth execution of clinical trials.Key Responsibilities:Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up...

  • Clinical Trials Coordinator

    2 weeks ago

    Reading, Reading, United Kingdom Pharmiweb Full time

    Job OverviewAs a Clinical Trials Assistant at Pharmiweb, you will play a vital role in ensuring the successful delivery of clinical trials. Your primary responsibility will be to provide administrative support to the clinical research team, ensuring that all clinical documents and systems are accurately updated and maintained.Key Responsibilities Assist the...

  • Clinical Trials Coordinator

    2 weeks ago

    Reading, Reading, United Kingdom Pharmiweb Full time

    Job OverviewAs a Clinical Trials Assistant at Pharmiweb, you will play a vital role in ensuring the smooth execution of clinical trials. Your primary responsibility will be to assist the clinical team with daily administrative activities, including updating and maintaining clinical documents and systems, such as the Trial Master File (TMF), to track site...

  • Clinical Trial Coordinator

    1 month ago

    Reading, United Kingdom Verbatim Pharma Full time

    Verbatim Pharma is working with a global company based in Reading, UK. The company is a global service partner for pharmaceutical and biotech firms, specialising in clinical trial services.The company has a great company culture that is friendly, energetic, and multi-cultural. Employees from various backgrounds work together, speaking a range of languages....

  • Clinical Trial Coordinator

    1 month ago

    Reading, United Kingdom Verbatim Pharma Full time

    Verbatim Pharma is working with a global company based in Reading, UK. The company is a global service partner for pharmaceutical and biotech firms, specialising in clinical trial services.The company has a great company culture that is friendly, energetic, and multi-cultural. Employees from various backgrounds work together, speaking a range of languages....

  • Clinical Trials Coordinator

    3 weeks ago

    Reading, Reading, United Kingdom Pharmiweb Full time

    Job OverviewAs a Clinical Trials Assistant, you will play a crucial role in ensuring the smooth execution of clinical trials. Your primary responsibility will be to provide administrative support to the Clinical Research Associates and Regulatory and Start-Up teams.Key Responsibilities Assist in maintaining clinical documents and systems, including the Trial...

  • Clinical Trial Coordinator

    3 weeks ago

    Reading, United Kingdom Verbatim Pharma Full time

    Verbatim Pharma is working with a global company based in Reading, UK. The company is a global service partner for pharmaceutical and biotech firms, specialising in clinical trial services.The company has a great company culture that is friendly, energetic, and multi-cultural. Employees from various backgrounds work together, speaking a range of languages....

  • Clinical Trial Coordinator

    3 weeks ago

    Reading, United Kingdom Verbatim Pharma Full time

    Verbatim Pharma is working with a global company based in Reading, UK. The company is a global service partner for pharmaceutical and biotech firms, specialising in clinical trial services.The company has a great company culture that is friendly, energetic, and multi-cultural. Employees from various backgrounds work together, speaking a range of languages....

  • Clinical Trial Coordinator

    3 weeks ago

    Reading, Reading, United Kingdom Verbatim Pharma Full time

    Verbatim Pharma is working with a global company based in Reading, UK. The company is a global service partner for pharmaceutical and biotech firms, specialising in clinical trial services.The company has a great culture that is friendly, energetic, and multi-cultural. Employees from various backgrounds work together, speaking a range of languages. If you...

  • Clinical Trial Coordinator

    3 weeks ago

    Reading, Reading, United Kingdom Verbatim Pharma Full time

    Verbatim Pharma is working with a global company based in Reading, UK. The company is a global service partner for pharmaceutical and biotech firms, specialising in clinical trial services.The company has a great culture that is friendly, energetic, and multi-cultural. Employees from various backgrounds work together, speaking a range of languages. If you...

  • Clinical Trials Coordinator

    2 weeks ago

    Reading, Reading, United Kingdom Pharmiweb Full time

    Job OverviewAt Pharmiweb, we are seeking a highly organized and detail-oriented Clinical Trials Assistant to support our clinical research team. The successful candidate will be responsible for performing daily administrative activities, including updating and maintaining clinical documents and systems, and assisting with the preparation and handling of...

  • Clinical Trial Supply Coordinator

    3 weeks ago

    Reading, Reading, United Kingdom Verbatim Pharma Full time

    Verbatim Pharma is working with a global company based in Reading, UK. The company is a global service partner for pharmaceutical and biotech firms, specialising in clinical trial services.The company has a great company culture that is friendly, energetic, and multi-cultural. Employees from various backgrounds speak a range of languages, creating a dynamic...

  • Senior Clinical Trial Assistant

    5 months ago

    Reading, United Kingdom Novasyte Full time

    Do you want to grow your career with the World’s largest CRO? Our Sponsor Dedicated team are recruiting for a Senior Clinical Trial Assistant to join us on our mission to drive healthcare forward. IQVIA offer genuine career progression (named on LinkedIn’s Top Companies: The 25 best workplaces to grow your career in the UK), supportive leadership, team...

  • German Speaking Project Coordinator

    2 weeks ago

    Reading, United Kingdom Verbatim Pharma Full time

    Verbatim Pharma is a global service partner for pharmaceutical and biotech firms, specialising in clinical trial services. We are looking for a skilled project coordinator with fluent German and English language skills to join our team.Main responsibilities:Be the first point of contact for clinical trial sponsors, CROs and CMOsOversee orders and delivery...

  • Clinical Trial Coordinator

    5 months ago

    Reading, United Kingdom Clintec Full time

    Job Overview Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning. This role offers hybrid working, with 2-3 days on site...

  • Clinical Trial Manager

    2 weeks ago

    Reading, Reading, United Kingdom ENGINEERINGUK Full time

    Clinical Trial Manager - Sponsor DedicatedAt ENGINEERINGUK, we're seeking a Clinical Trial Manager to oversee the planning, execution, and successful completion of clinical trials. As a leader in our research department, you'll collaborate with cross-functional teams, manage site relationships, and provide strategic guidance to drive the successful delivery...

Clinical Trial Coordinator

2 months ago

Reading, United Kingdom Pharmiweb Full time
Our sponsor dedicated (cFSP) team are seeking a Clinical Trial Coordinator to join us on our mission to drive healthcare forward.
Hybrid working on offer, with 3 days per week required on-site in Central London with the sponsor, a large multinational pharmaceutical.
The Clinical Trial Coordinator will perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrolment in clinical studies.
Essential Functions
• Provide clinical research support to investigators to prepare for and execute assigned research studies, including:
• Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data;
• Attend all relevant study meetings;
• Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research;
• Recruit and screen patients for clinical trials and maintain subject screening logs;
• Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits;
• Design and maintain source documentation based on protocol requirements;
• Schedule and execute study visits and perform study procedures;
• Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness;
• Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics;
• Monitor subject safety and report adverse reactions to appropriate medical personnel;
• Correspond with research subjects and troubleshoot study-related questions or issues;
• Participate in “huddles” to confirm daily study tasks are assigned to team members and are executed to the expected standards;
• Assist with study data quality checking and query resolution.
• Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring.
• Record, report and interpret study findings appropriately to develop a study-specific database.
• Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards.
• Provide training to new investigator site staff members on study-specific topics and requirements. Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.
• Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.
• Assist research site with coverage planning related to staffing and scheduling for research projects.
Qualifications
• Bachelor's Degree (science) or equivalent industry experience
• Minimum 6 months relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training and experience
• Working knowledge of clinical trials
• Working knowledge of the principles of Good Clinical Practices (GCP)
• Skill in carrying out required clinical procedures
• Good skill in using MS Windows and Office applications such as Access, Outlook and Word
• Excellent interpersonal skills
• Ability to pay close attention to detail
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at