LEAD CRA FREELANCE 0.5 FTE - REMOTE (ITALY)
LEAD CRA FREELANCE 0.5 FTE - REMOTE (ITALY)
LEAD CRA FREELANCE 0.5 FTE - REMOTE (ITALY)
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities resourcing and functional service (FSP) solutions.
Key Responsibilities
Support the Project Manager being responsible and accountable for overseeing all aspects of monitoring and site Management activities ensuring compliance with ICH/GCP guidelines SOPs and protocol requirements.
Lead manage and guide CRAs being responsible for training and quality oversight of site management activities while proactively identifying potential operational issues and ensuring study deliverables.
Development of Study Monitor plans Monitor and Site Training plans verification initiatives coordinating Study Investigator Meetings and reviewing site and country Study Reports.
Ensure study processes procedures and expectations correspond to the practicality of conducting the trial from study feasibility through to close out.
Serve as initial point of contact for the monitoring team and support them with investigative site personnel liaison.
Implement monitoring/recruitment plans and support also the design of CRF completion guidelines.
Perform co-monitoring visits as part of the monitoring team quality oversight.
Review and approve site visit reports (PSV SIV MV and COV) and act as first point of contact for issue escalation ensuring the proper resolution and action plan definition and follow up.
Review CRA Site Visits calendar ensuring monitoring visits (both remotely and on site) are being scheduled and conducted following monitoring plan frequency.
Update the Project Manager with status of sites and countries and ensure a proper escalation of any issue detected at site/country level.
Ensure documents remain current during the course of the trial and ensure proper maintenance of Trial Master File being responsible of QC when delegated by Project Manager.
When delegated by Project Manager track and approve investigators payments.
Assist Project Manager in CRA training program training CRAs on study procedures and requirements and ensuring a proper handover when there is a replacement of CRA.
Qualifications:
Bachelors Degree preferably in life science or nursing; or equivalent
Minimum 3 years of experience as CRA including relevant on-site monitoring experience.
Experience in Phase 4 / RWE / Non-Interventional Studies
Experience in Oncology ideally Breast Cancer
Understand the basic medical terminology and science associated with the assigned drugs and therapeutic areas
Possess the understanding of Good Clinical Practice regulations ICH guidelines
Ability to work independently as well as in a team matrix organization and multiple projects
Excellent written and verbal communication skills as well as computer skills
Excellent organizational and Line Management skills
Ability and willingness to travel up to 10-20%
What We Offer
We provide a competitive compensation package comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. Youll be joining a team that values collaboration innovation and making a difference in the lives of patients
A Bit More About Us
Our journey began over 27 years ago in Sweden in the city of Lund. As a full-service global Contract Research Organization (CRO) we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology Neuroscience Oncology and Ophthalmology.
Our core values of Trust Quality Passion Flexibility and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments resulting in high employee engagement and satisfaction. By aligning on these fundamental values we cultivate a unified force geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.
LEAD CRA FREELANCE 0.5 FTE - REMOTE (ITALY)LEAD CRA FREELANCE 0.5 FTE - REMOTE (ITALY)LEAD CRA FREELANCE 0.5 FTE - REMOTE (ITALY)TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire c...
LEAD CRA FREELANCE 0.5 FTE - REMOTE (ITALY)
LEAD CRA FREELANCE 0.5 FTE - REMOTE (ITALY)
LEAD CRA FREELANCE 0.5 FTE - REMOTE (ITALY)
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities resourcing and functional service (FSP) solutions.
Key Responsibilities
Support the Project Manager being responsible and accountable for overseeing all aspects of monitoring and site Management activities ensuring compliance with ICH/GCP guidelines SOPs and protocol requirements.
Lead manage and guide CRAs being responsible for training and quality oversight of site management activities while proactively identifying potential operational issues and ensuring study deliverables.
Development of Study Monitor plans Monitor and Site Training plans verification initiatives coordinating Study Investigator Meetings and reviewing site and country Study Reports.
Ensure study processes procedures and expectations correspond to the practicality of conducting the trial from study feasibility through to close out.
Serve as initial point of contact for the monitoring team and support them with investigative site personnel liaison.
Implement monitoring/recruitment plans and support also the design of CRF completion guidelines.
Perform co-monitoring visits as part of the monitoring team quality oversight.
Review and approve site visit reports (PSV SIV MV and COV) and act as first point of contact for issue escalation ensuring the proper resolution and action plan definition and follow up.
Review CRA Site Visits calendar ensuring monitoring visits (both remotely and on site) are being scheduled and conducted following monitoring plan frequency.
Update the Project Manager with status of sites and countries and ensure a proper escalation of any issue detected at site/country level.
Ensure documents remain current during the course of the trial and ensure proper maintenance of Trial Master File being responsible of QC when delegated by Project Manager.
When delegated by Project Manager track and approve investigators payments.
Assist Project Manager in CRA training program training CRAs on study procedures and requirements and ensuring a proper handover when there is a replacement of CRA.
Qualifications:
Bachelors Degree preferably in life science or nursing; or equivalent
Minimum 3 years of experience as CRA including relevant on-site monitoring experience.
Experience in Phase 4 / RWE / Non-Interventional Studies
Experience in Oncology ideally Breast Cancer
Understand the basic medical terminology and science associated with the assigned drugs and therapeutic areas
Possess the understanding of Good Clinical Practice regulations ICH guidelines
Ability to work independently as well as in a team matrix organization and multiple projects
Excellent written and verbal communication skills as well as computer skills
Excellent organizational and Line Management skills
Ability and willingness to travel up to 10-20%
What We Offer
We provide a competitive compensation package comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. Youll be joining a team that values collaboration innovation and making a difference in the lives of patients
A Bit More About Us
Our journey began over 27 years ago in Sweden in the city of Lund. As a full-service global Contract Research Organization (CRO) we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology Neuroscience Oncology and Ophthalmology.
Our core values of Trust Quality Passion Flexibility and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments resulting in high employee engagement and satisfaction. By aligning on these fundamental values we cultivate a unified force geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.
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