YouV Lifesciences Solutions Private Limited is hiring an experienced Clinical Trial Assistant (CTA) for a remote position based in Bengaluru. The opportunity is suitable for clinical research professionals with 1+ year of experience, particularly candidates who have worked directly with investigator sites, Investigators, site staff, regulatory documentation, and eTMF/TMF activities.
The selected candidate will support clinical research activities across the study lifecycle, including site start-up, ongoing study management, regulatory documentation, essential document management, eTMF activities, and study close-out.
This remote Clinical Trial Assistant job may be particularly relevant for professionals with previous Clinical Research Coordinator (CRC) or investigator-site experience.
Job Details
| Details | Information |
|---|---|
| Company | YouV Lifesciences Solutions Private Limited |
| Position | Clinical Trial Assistant (CTA) |
| Job Type | Full-time |
| Location | Bengaluru, Karnataka – Remote |
| Experience | 1+ years |
| Industry | Clinical Research / Life Sciences |
| Work Mode | Remote |
| Joining Preference | Immediate Joiners |
| Application Email | CV@youvresearch.com |
Clinical Trial Assistant Responsibilities
The Clinical Trial Assistant will be responsible for supporting clinical trial activities and maintaining accurate study documentation.
Key responsibilities include:
- Coordinate clinical research activities with investigator sites in the USA.
- Communicate remotely with Investigators and site staff.
- Manage and maintain site regulatory documents and essential clinical trial documentation.
- Support eTMF/TMF management, including document collection, review, tracking, filing, and reconciliation.
- Ensure site documentation is complete, accurate, current, and maintained according to applicable requirements.
- Support clinical trial site start-up activities.
- Assist with ongoing study activities and study close-out documentation.
- Track regulatory submissions, approvals, renewals, amendments, and other site documentation.
- Follow up with investigator sites regarding missing or outstanding documents.
- Support timely resolution of documentation issues.
- Maintain effective communication and appropriate documentation throughout the clinical study lifecycle.
- Manage multiple studies or tasks while maintaining attention to detail.
Qualifications for Clinical Trial Assistant Job
Candidates applying for the Clinical Trial Assistant (CTA) position should have:
- At least 1 year of experience in clinical research.
- Experience as a Clinical Research Coordinator (CRC) or in a similar investigator-site role is preferred.
- Hands-on experience working with Investigators and clinical trial sites.
- Knowledge of clinical research processes and regulatory documentation.
- Understanding of essential clinical trial documents.
- Experience with eTMF/TMF documentation and management.
- Good understanding of Good Clinical Practice (GCP).
- Knowledge of clinical trial regulations and site documentation requirements.
- Strong written and verbal communication skills.
- Excellent attention to detail.
- Ability to manage multiple studies and tasks.
- Ability to work independently in a remote environment.
- Immediate joiners are preferred.
Who Can Apply?
This opportunity can be relevant to professionals with backgrounds such as:
- Clinical Research
- Clinical Research Coordinator
- Clinical Trial Assistant
- Clinical Trial Operations
- Site Management
- Clinical Operations
- eTMF / TMF Management
- Regulatory Documentation
- Clinical Research Associate support functions
Candidates should prioritize the employer’s stated requirements, particularly investigator-site experience, eTMF/TMF knowledge, GCP understanding, and clinical research experience.
Work Location
The position is listed as Bengaluru, Karnataka, with remote working. The role involves working with investigator sites in the USA, so candidates should be comfortable with remote communication and coordinating with international clinical research stakeholders.
Salary
The original job advertisement does not specify a salary range.
For SEO/schema purposes, a salary range should not be presented as an employer-confirmed figure. If a salary must be displayed on Pharmabharat, label it clearly as an estimated market range, rather than representing it as the company’s offered compensation.
Suggested editorial estimate: ₹3.5–₹7.0 lakh per annum, depending on experience and relevant clinical research/eTMF expertise.
How to Apply
Interested candidates can apply by sending their updated CV to:
