Remote CRA Job at TFS HealthScience | Apply Now
Remote CRA Job opportunities are expanding across the global clinical research sector, and TFS HealthScience is hiring a Clinical Research Associate (CRA) for its Clinical Development Services (CDS) – Ophthalmology team. This fully remote contract role based in Kefar Sava, Tel Aviv offers professionals with a background in life sciences or clinical research the opportunity to contribute to international clinical trials while working remotely. This Life Sciences Job supports study monitoring, compliance, and clinical trial quality.
About TFS HealthScience
Remote CRA job seekers looking for TFS HealthScience careers will find exciting opportunities with a leading global mid-size Contract Research Organization (CRO). TFS HealthScience partners with biotechnology and pharmaceutical companies throughout the entire clinical development journey by providing full-service capabilities, Functional Service Provider (FSP) solutions, and strategic resourcing.
Founded more than 30 years ago in Lund, Sweden, TFS HealthScience now has over 600 professionals delivering tailored clinical research services across more than 50 countries. The company supports multiple therapeutic areas, including Dermatology, Neuroscience, Oncology, and Ophthalmology, while maintaining a strong commitment to Trust, Quality, Passion, Flexibility, and Sustainability.
Job Details
| Company | TFS HealthScience |
| Job Title | Clinical Research Associate (CRA) |
| Department | Clinical Development Services (CDS) – Ophthalmology |
| Location | Kefar Sava, Tel Aviv (Fully Remote) |
| Employment Type | Fully Remote |
| Qualification | Bachelor’s Degree, preferably in Life Sciences, or equivalent |
| Experience | Minimum 1 year of relevant clinical research experience or relevant academic background related to clinical trials or clinical development activities |
Job Description – Remote CRA Job
This Remote CRA Job involves working within the Clinical Development Services (CDS) team as a Clinical Research Associate (CRA). The selected candidate will support study site initiation, conduct on-site and remote monitoring visits, and manage study close-out activities. The role requires ensuring that all clinical trial operations align with company policies, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), ICH guidelines, sponsor requirements, and applicable regulatory standards.
The Clinical Research Associate will focus on maintaining participant safety, ensuring protocol compliance, and safeguarding data integrity throughout the clinical trial lifecycle. The position includes collaboration with cross-functional teams while independently managing assigned study sites.
Eligibility Criteria
Remote CRA Job qualifications include:
- Education: Bachelor’s Degree, preferably in Life Sciences, or equivalent.
- Experience: Minimum 1 year of relevant clinical research experience or relevant academic background related to clinical trials or clinical development activities.
- Language: Strong written and verbal communication skills with fluency in English.
Required Skills
- Understanding of Good Clinical Practice (GCP), ICH guidelines, and applicable regulatory requirements.
- Strong written and verbal communication skills.
- Excellent organizational skills.
- Ability to work independently.
- Ability to work within a matrix team environment.
- Attention to detail in documentation and reporting.
Remote CRA Job – Key Responsibilities
- Monitor on-site and remotely clinical trials in accordance with TFS and/or sponsor Standard Operating Procedures, GCP and ICH guidelines, and applicable regulatory requirements.
- Perform all required monitoring activities at study sites to ensure subject safety, data integrity, and quality.
- Verify the protection of study participants through informed consent procedures and protocol compliance in accordance with regulatory requirements.
- Review CRFs (electronic or paper) and subject source documentation for validity, completeness, and accuracy.
- Verify proper management and accountability of Investigational Product.
- Prepare timely monitoring visit reports, document findings and follow-up actions, update required tracking systems, and escalate issues as appropriate.
- Ensure site documentation is maintained appropriately.
- Support eTMF and ISF compliance and update CTMS and other required project systems with accurate site information.
If you are seeking a Remote CRA Job with a Contract Research Organization supporting global clinical development, this Clinical Research Associate position at TFS HealthScience offers remote flexibility and hands-on trial monitoring responsibilities. This Life Sciences Job enables professionals to strengthen their clinical research expertise while contributing to regulated study environments.
