Study Nurse Freelance

About this role

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.

The Study Nurse coordinates and manages clinical studies with drugs medical devices and cosmetics as Study Nurse under the supervision of the Principal Investigator (PI) in cooperation with the TFS In-house Clinic study team according to the policies and Standard Operating Procedures of TFS and in compliance with Good Clinical Practice as well as with the national and international regulations for clinical studies and data protection

Key Responsibilities

Study Set-up:
- Complete feasibility questionnaires from Sponsors
- Prepare and attend Pre-study visits
- Complete the site qualification questionnaire for EC submission
- Participate in the investigator meetings of the Sponsors
- Plan and attend Site Initiation Visits
- Support patient recruitment in collaboration with the investigators

Study Conduct according to the protocol-related tasks delegated by the PI:
- Coordinate prepare and conduct patients visits according to the study protocol and support the investigators also in screening activities
- Conduct diagnostic tests such as vital signs etc.
- Collect and process biological samples
- Manage laboratory shipping logistics
- Dispense and administer the Investigational Medicinal Product to study participants
following the instructions of the investigators
- Manage the Drug Accountability including storage preparation of the Investigational
Medicinal Product
- Main contact person for communication with study participants CRAs and Sponsors
- Manage patients reimbursements and investigator fees

Study project documentation:
- Prepare and maintain patient files for source documentation
- Capture Source Data in various electronic or paper-based Data Capture Systems
- Resolve Data Queries in collaboration with the investigators
- Maintain the Investigator Site Files
- Assist in Serious Adverse Event reporting
- Prepare support and post-process monitoring visits and audits/inspections
- Archive study documents

Qualifications

- Work Experience as Study Nurse (2 years ideally)
- Excellent organizational skills ability to prioritise and handle multiple competing priorities and timelines
- Excellent verbal and written communication skills
- Ability to work independently and in a team
- Knowledge of the Good Clinical Practice
- Very good command of written and spoken English
- Good knowledge of MS Office
- Willingness to travel on occasion

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.