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Clinical Research Associate
hace 1 mes
TFS HealthScience Overview
As a leading global Contract Research Organization (CRO), TFS HealthScience partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. With expertise in full-service capabilities, resourcing, and Functional Service (FSP) solutions, we deliver tailored clinical research services in over 40 countries.
About the Role
We are seeking an experienced Clinical Research Associate to join our Strategic Resourcing Solutions team. As part of this team, you will work alongside passionate and innovative professionals to ensure our customers achieve their goals.
In this role, you will be responsible for the initiation, on-site and remote monitoring, and termination of investigative sites during study conduct. You will also conduct all stages of site monitoring, including feasibility, pre-study, initiation, interim, and close-out. Ability to travel as needed is required, which may involve overnight and international travel.
Key Responsibilities:- Conduct on-site and remote monitoring of clinical trials according to company policies, SOPs, and regulatory requirements.
- Review CRFs (paper or electronic) and subject source documentation for validity and accuracy and generate queries to investigational sites/clients to resolve problem data.
- Identify site problems/deficiencies and bring them to the attention of management through trip reporting, memos, and verbal communication with Project Manager or Lead CRA.
- Initiate corrective action to resolve issues as directed by supervisor.
- Contribute to the completion of the application to Ethics Committee/IRB, prepare necessary documentation enclosed to the application according to local requirements in cooperation with CTA and directed by Lead CRA/Project Manager.
- Participate in contract handling and negotiation directed by Lead CRA/Project Manager.
Qualifications
- Bachelor's Degree, preferably in life science or nursing or equivalent.
- Minimum 1-3 years of relevant clinical experience.
- Able to work in a fast-paced environment with changing priorities.
- Understand basic medical terminology and science associated with assigned drugs and therapeutic areas.
- Possess understanding of Good Clinical Practice regulations, ICH guidelines.
What We Offer
We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You'll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.
Our salary range for this position is approximately $60,000-$80,000 per year, depending on qualifications and experience.
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 guide our decision-making at all levels of the organization. They help us attract and retain 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.
