Posted Aug 2, 2022
TFS is a Global CRO headquartered in Sweden. We genuinely believe that “Global in mind and local at heart” is the core of our success; we operate in a global environment while retaining an in-depth knowledge of regulatory requirements in every country where we operate. At TFS, you will be offered the possibility to develop in a global organization with a company culture distinguished by passion, innovation and talent.
As a CRA, you will be a member of the Study Team and the Project Delivery and will be responsible for coordination of operational activities, such as coordination of monitoring activities, and integration with other departments according to company policies, SOPs and regulatory requirements.
Key responsibilities include:
- Monitor on-site and remotely clinical trials in accordance with TFS and/or client company Standard Operating Procedures, FDA regulations, and GCP and ICH guidelines
- 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 to the attention of management through trip reporting, memos, and verbal communication with Project Manager or Lead CRA
- Initiates 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
- Set up ISF and SMF (or cooperate with CTA) and distribute to the investigational sites.
- In cooperation with study team, responsible for SMF maintenance
- Order, ship, and reconcile clinical investigative supplies for study sites, if applicable
- Order, ship and coordination of study supplies at site
- May prepare and submit status reports as directed by Lead CRA/PM
- Review and support site staff to maintain SMF
- Review Informed Consent documents for essential elements and protocol specifics
- Update CTMS system with site and study information
- May audit data in tables and text of clinical summaries
- May assist in the preparation of study documentation such as CRF Completion Guidelines, patient diaries, study participation cards by reviewing for accuracy and completeness
- Bachelor’s Degree, preferably in life science or nursing; or equivalent
- Minimum 5 years of relevant clinical experience
- Experience in Ophthalmology or Oncology.
- Experience with EC submissions
- Able to work in a fast paced environment with changing priorities
- Understand 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
- Excellent written and verbal communication skills.
- Excellent organizational skills
- Ability and willingness to travel up to 60%
- Private Health Coverage
- Corporate Pension Plan
- Life Insurance
- Global General Liability Insurance
- Global Travel Insurance
- Home-based Allowance
- Internet reimbursement
- Car Allowance
- Flexible working schedule