Life Sciences Job at TFS HealthScience, Sweden | Apply Online
If you are a clinical data coordinator or a patient enrollment specialist looking to apply your study coordination skills within a world-class clinical research framework, this position at TFS HealthScience is an exceptional opportunity. Available across multiple strategic healthcare hubs in Sweden, this on-site role embeds you directly into active investigator site operations. For organized laboratory and clinic professionals searching for a high-impact Life Sciences Job, this position offers direct ownership of electronic Case Report Form (eCRF) data entry, investigator site file auditing, and patient visit logistics. It serves as an elite operational launchpad for a long-term TFS HealthScience career and stands out as a premier Life Sciences Job in Sweden within a premium, dedicated pharmaceutical sponsor model.
- Job Position: Study Coordinator
- Locations: Stockholm, Lund, Askersund, Gothenburg, Malmö, Solna, Uppsala
- Req ID: 471648
About The Company
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. Founded over 30 years ago in Lund, Sweden, TFS has scaled to bring together over 600 professionals operating in more than 50 countries, delivering tailored clinical trials across key therapeutic areas such as Dermatology, Neuroscience, Oncology, and Ophthalmology.
Through the Strategic Resourcing Solutions (SRS) and Functional Service Provider (FSP) framework, TFS deploys dedicated study specialists directly into localized investigator sites. In this model, you are fully dedicated to a single sponsor—a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area—combining the robust infrastructure of a premier CRO with deep site-level execution.
Life Sciences Job – Key Responsibilities
Operating under the direct supervision of the clinic’s Principal Investigator (PI), you will perform delegated site-study tasks to optimize data quality, accelerate data-entry processes, and support critical enrollment milestones.
Your core clinical coordination, data entry, and tracking duties will include:
- High-Volume Data Entry: Processing clinical data streams and entering study parameters precisely into Electronic Data Capture (EDC) frameworks to advance this Life Sciences Job.
- Query Resolution: Reviewing data discrepancies flagged by monitoring teams and working cross-functionally with site staff to clean data listings.
- Patient Recruitment & Scheduling: Assisting investigators with active patient recruitment initiatives, pre-screening logs, and managing complex patient visit schedules.
- Safety & Ethics Administration: Assisting with serious adverse event (SAE) notification timelines and facilitating localized Ethics Committee tracking submissions.
- Monitoring Visit Governance: Preparing the Investigator Site File (ISF) for routine monitoring visits, corporate quality audits, and official health authority inspections.
- Drug & Sample Logistics: Maintaining study drug accountability records, dispensing logs, and performing non-invasive clinical sample management to secure a compliant Life Sciences Job in Sweden workflow.
Qualifications & Profile Requirements For Life Sciences Job
This vacancy is meticulously tailored for detail-oriented, administrative monitors who possess strong Good Clinical Practice (GCP) habits and a collaborative clinic mindset.
- Educational Foundation: A formal educational background in clinical research, or a related quantitative life sciences discipline.
- Professional Credentials: An active, verifiable GCP Certification in compliance with international and local clinical trial legislation.
- Site Coordination Track Record: Proven previous experience handling core site coordination duties, including patient visit scheduling, monitoring visit preparation, and data logging.
- Technical Software Skills: Hands-on familiarity navigating standard eCRF or EDC systems (such as Medidata Rave, Viedoc, or Oracle InForm) to accelerate your TFS HealthScience career.
- Linguistic Mastery: Full professional fluency in Swedish is mandatory to interact with local patient populations and clinic investigators, paired with strong proficiency in English.
In short, the Study Coordinator position at TFS HealthScience is a definitive route to transitioning your clinical background into a highly marketable, international operations portfolio. Securing this appointment allows you to step away from isolated administrative tasks and take primary operational charge of the eCRF data streams, investigator files, and sponsor relationships that steer multi-center clinical trials. If you live in Sweden, hold an active GCP certification, and possess the drive to speed up database lock timelines, apply today to secure this premier Life Sciences Job, launch a highly rewarding TFS HealthScience career, and lock in this outstanding Life Sciences Job in Sweden.
