Are you an experienced clinical research professional looking to advance your career with a growing organization in the pharmaceutical and clinical research industry? Here’s an exciting opportunity for professionals with experience in Clinical Operations and CRO environments.

YouV Lifesciences Solutions Private Limited is hiring In-house Clinical Research Associates (CRA) for its Clinical Operations team in Bengaluru. This hybrid role is ideal for candidates with 1–3 years of experience who possess strong knowledge of ICH GCP guidelines, TMF/eTMF, CTMS, and EDC systems.

If you’re passionate about supporting global clinical trials while building expertise in clinical operations, this opportunity could be the perfect next step in your career.

🏢 About YouV Lifesciences Solutions

YouV Lifesciences Solutions Private Limited provides specialized clinical research and scientific solutions to global pharmaceutical, biotechnology, and healthcare organizations.

The company focuses on:

Clinical Operations
Clinical Trial Management
Regulatory Compliance
Scientific Documentation
Quality Management
Clinical Data Support

Working at YouV Lifesciences gives professionals exposure to international clinical trials, global quality standards, and modern clinical technologies.

📌 Job Details

Particular	Details
Company	YouV Lifesciences Solutions Private Limited
Position	In-house Clinical Research Associate (CRA)
Department	Clinical Operations
Job Type	Full-Time
Work Model	Hybrid
Location	Bengaluru, Karnataka
Experience Required	1–3 Years
Industry	Clinical Research / CRO
Application Mode	Email

🎓 Educational Qualification

Candidates with any of the following qualifications are encouraged to apply:

B.Pharm
M.Pharm
B.Sc (Life Sciences)
M.Sc
B.Tech (Biotechnology)
M.Tech
Nursing
Biotechnology
Life Sciences
Other relevant healthcare disciplines

💼 Experience Required

Applicants should have:

1–3 years of Clinical Research experience
Previous CRO experience preferred
Experience supporting clinical trials
Familiarity with regulatory documentation
Good understanding of investigator site management

📚 Required Skills

The ideal candidate should possess:

Strong understanding of ICH GCP E6(R3)
Clinical trial documentation knowledge
Experience with TMF/eTMF
Knowledge of Clinical Trial Management Systems (CTMS)
Experience using Electronic Data Capture (EDC) platforms
Excellent documentation skills
Strong organizational abilities
Good communication skills
Attention to detail
Ability to coordinate multiple stakeholders

🛠 Key Responsibilities

As an In-house CRA, your responsibilities will include:

📂 Trial Master File Management

Maintain TMF/eTMF documentation
Review essential clinical documents
Archive study files
Ensure inspection readiness

📑 Regulatory Documentation

Manage documents such as:

Investigator CVs
Ethics Committee approvals
Informed Consent Forms (ICFs)
Regulatory submissions
Essential study documents

🤝 Site Coordination

Support investigator sites remotely
Coordinate with field CRAs
Resolve site queries
Track document submissions

📊 Clinical Trial Support

Monitor study progress
Review monitoring reports
Track patient recruitment
Maintain study timelines

💻 Clinical Systems Management

Update and maintain:

CTMS
EDC
eTMF
Study trackers
Trial metrics

✅ Regulatory Compliance

Ensure studies comply with:

ICH GCP E6(R3)
Study protocols
Sponsor requirements
Regulatory guidelines
Quality standards

🌟 Why Join YouV Lifesciences?

Working at YouV Lifesciences offers several career advantages:

✅ Hybrid working model

✅ Opportunity to work on global clinical trials

✅ Exposure to advanced Clinical Operations

✅ Strong learning environment

✅ Career growth opportunities

✅ Experience with industry-standard clinical systems

✅ Collaborative work culture

✅ Professional development

🚀 Career Growth Opportunities

This role can help professionals progress toward positions such as:

Senior Clinical Research Associate
Lead CRA
Clinical Trial Associate
Clinical Project Coordinator
Clinical Project Manager
Clinical Operations Lead
Trial Master File Specialist
Clinical Operations Manager

📧 How to Apply?

Interested candidates can apply by following the steps below:

Step 1

Prepare an updated resume highlighting:

Clinical Research experience
CRO experience
TMF/eTMF expertise
CTMS knowledge
EDC experience
ICH GCP knowledge

Step 2

Email your updated CV to:

📧 CV@youvresearch.com

Step 3

Use the mandatory subject line:

Application for Inhouse CRA

💡 Resume Tips

To improve your chances of getting shortlisted:

Highlight clinical trial experience
Mention therapeutic areas worked on
Include TMF/eTMF experience
List CTMS and EDC platforms used
Mention ICH GCP certification (if applicable)
Quantify your achievements where possible

📍 Job Location

Bengaluru, Karnataka

This position follows a Hybrid Work Model, allowing employees to work both remotely and from the office depending on business requirements.

🔥 Why Clinical Operations is a Great Career in 2026

Clinical Operations continues to be one of the fastest-growing domains in the pharmaceutical and biotechnology sectors. With increasing global clinical trials and stronger regulatory requirements under the latest ICH GCP guidelines, skilled professionals in Clinical Operations are in high demand.

Professionals experienced in TMF management, CTMS, EDC systems, and regulatory compliance enjoy excellent career progression, competitive salaries, and opportunities to work on global drug development programs.

📢 Final Thoughts

If you have 1–3 years of Clinical Research experience and are looking for a rewarding opportunity in Clinical Operations, the YouV Lifesciences In-house Clinical Research Associate role offers an excellent platform to grow your career.

The hybrid work environment, exposure to international clinical trials, and opportunities to develop expertise in TMF, CTMS, EDC, and regulatory compliance make this an ideal role for ambitious clinical research professionals.

Don’t miss this opportunity—prepare your resume and apply today!

📌 Job Summary

Details	Information
Company	YouV Lifesciences Solutions Private Limited
Role	In-house Clinical Research Associate (CRA)
Location	Bengaluru (Hybrid)
Experience	1–3 Years
Qualification	B.Pharm, M.Pharm, B.Sc, M.Sc, B.Tech, M.Tech, Nursing, Biotechnology, Life Sciences
Department	Clinical Operations
Application Mode	Email
Email	CV@youvresearch.com
Subject Line	Application for Inhouse CRA

YouV Lifesciences Hiring In-house Clinical Research Associate (CRA) 2026 | Hybrid Clinical Operations Job in Bengaluru