Clinical Trial Assistant (CTA)
TFS, Sweden
Job Description
TFS HealthScience is excited to be expanding our Strategic Resourcing Solution team and we are looking for an experienced, highly motivated Clinical Trial Assistant (CTA) who shares our vision of providing clinical research excellence. Our Strategic Resourcing Solution team is a highly experienced international group of professionals led by an industry expert.
We are a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. We combine the full-service capabilities and global reach of a large CRO with the flexibility and personal approach only a mid-size CRO can deliver.
Our cores values of Trust, Quality, Flexibility and Passion are what makes TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization. Together we make a difference.
TFS HealthScience is looking for a Clinical Trial Assistant (CTA) office based in Stockholm, Sweden. We look forward to receiving your application!
The Clinical Trial Assistant (CTA) will work, when delegated, as a member of the study team with the responsibility to provide full administrative support for clinical projects according to Good Clinical Practice Guidelines. Responsible for administration of set up, monitoring, tracking and close out of clinical trials. Maintain project files and documentation in an orderly manner according to the company’s Standard Operation procedures (SOPs).
Key Responsibilities
- Set up SSF/eTMF, archive, track and update documents.
- Import relevant documents and data into different databases.
- Translate or administrate translation of documents to relevant language.
- Ensure study supplies/stationary at relevant location.
- Liaise with sites, clients, laboratories, drug suppliers and project team members.
- Provide administrative support for project team members.
- Assist in submission to Ethics committee and Regulatory authorities.
- Take minutes of project team meetings.
- Assist the Contract and Budget Administrator in preparing site contracts and amendments and managing invoice specifications and invoices with the respective tracking.
Requirements
- Bachelor’s Degree in relevant field
- 1+ years of experience in clinical research/drug development is preferred
- Understanding of FDA and ICH Guidelines, Good Clinical Practices (GCP), medical terminology, and clinical trials
- Computer skills including working knowledge of Microsoft Office Suite.
- Excellent written and verbal communication in Swedish and English.
- Effective time management and organizational skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Benefits
What can we offer you?
A great place to work where you will get the chance to push your career to the next level, global environment with global opportunities. You will also get the opportunity to be part of a team with highly intelligent, passionate experts from all over the world. TFS HealthScience is a place for inspiration where we focus on the patients, saving lives and aiming to increase their quality of life by supporting our clients. Sweden benefits include:
- Competitive salary amp; benefits package
- Excellent career progression opportunities
- Great corporate culture and work life balance
- Health Insurance
- Corporate pension plan
- Global General Liability Insurance
- Global Travel Insurance
- Flexible working schedule