Veeda Lifesciences CRA Recruitment for Pharma Roles
- Veeda Lifesciences Hiring Clinical Research Associate – High Demand Clinical Trials Role in Ahmedabad
- Company Overview
- Job Role & Responsibilities
- Off-site Monitoring
- Communication & Documentation
- Audits & Compliance
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What skills are important for a Clinical Research Associate?
- What is the career growth after CRA?
- Is this a high-paying pharma job?
- Summary
Veeda Lifesciences Hiring Clinical Research Associate – High Demand Clinical Trials Role in Ahmedabad
Veeda Lifesciences is actively hiring for Clinical Research Associate (CRA) roles in Ahmedabad, Gujarat. This is a full-time, on-site opportunity for candidates looking to build or advance a career in clinical research, pharmacovigilance, and clinical trials management. With strong demand in the pharma and CRO sector, this role offers exposure to regulatory compliance, site monitoring, and clinical data management in real-world studies.
If you are aiming to work in high-paying clinical research jobs in India with long-term growth in pharma R&D and clinical operations, this opportunity is worth serious consideration.
Company Overview
Veeda Lifesciences is a well-established Contract Research Organization (CRO) in India, known for delivering high-quality clinical research, bioavailability and bioequivalence (BA/BE) studies, and regulatory-compliant services. The company supports global pharmaceutical and biotechnology firms with end-to-end clinical trial solutions.
With a strong reputation for data integrity, compliance with international guidelines, and ethical research practices, Veeda Lifesciences plays a key role in accelerating drug development and ensuring patient safety.
Job Role & Responsibilities
As a Clinical Research Associate, you will be responsible for managing and monitoring clinical trials, ensuring compliance with regulatory standards such as ICH-GCP guidelines.
Off-site Monitoring
- Conduct initial site visits to train and guide site personnel
- Ensure site readiness as per clinical trial protocol requirements
- Perform routine monitoring visits based on study timelines
- Oversee study progress and adherence to protocols
Communication & Documentation
- Coordinate feasibility assessments with clinical trial sites
- Prepare detailed reports including:
- Pre-study Qualification Reports
- Site Initiation Visit Reports
- Monitoring Visit Reports
- Closeout Visit Reports
- Collect essential documents such as calibration reports and agreements
- Ensure accurate data capture through logs, trackers, and source documents
Audits & Compliance
- Review study documentation in line with SOPs and regulatory guidelines
- Train and mentor site teams on GCP and protocol compliance
- Address audit queries from QA teams, sponsors, and regulatory authorities
- Support root cause analysis and corrective actions when required
Eligibility / Qualifications
Candidates applying for this clinical research job should meet the following criteria:
- Educational Qualification: B.Pharm, M.Pharm, Pharm.D, BSc (Life Sciences), MSc (Clinical Research, Biotechnology, Microbiology, Biochemistry), or equivalent
- Strong understanding of clinical trial processes and regulatory frameworks
- Knowledge of ICH-GCP guidelines and clinical data documentation
- Good communication and coordination skills
Location & Salary
- Job Location: Ahmedabad, Gujarat, India
- Work Mode: On-site
- Salary Range: ₹3.5 LPA – ₹6.5 LPA (approximate, based on industry standards for CRA roles in India)
Application Process
Interested candidates can apply directly through the official job listing using the link below:
Apply Here: https://www.linkedin.com/jobs/view/4406041484/
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
This role typically requires some understanding of clinical trials and regulatory processes. Candidates with relevant academic exposure or internships may be considered.
What skills are important for a Clinical Research Associate?
Attention to detail, knowledge of GCP guidelines, documentation skills, and communication abilities are essential.
What is the career growth after CRA?
You can progress to Senior CRA, Clinical Project Manager, or move into regulatory affairs and pharmacovigilance.
Is this a high-paying pharma job?
Yes, clinical research roles offer strong salary growth, especially with experience and certifications.
Summary
| Category | Details |
|---|---|
| Company | Veeda Lifesciences |
| Vacancies | Clinical Research Associate |
| Required Education | B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Clinical Research, Biotechnology, Microbiology, Biochemistry) |
| Experience | Not explicitly mentioned (preferred understanding of clinical research) |
To apply for this job please visit www.linkedin.com.
