Bio-Prospera Senior CRA Jobs | Clinical Research
Bio-Prospera Hiring Senior CRA in Mumbai | Clinical Research Jobs for Experienced Professionals
Professionals seeking Senior Clinical Research Associate jobs, Clinical Research jobs in Mumbai, or opportunities in the rapidly growing clinical trials industry have a promising opportunity with Bio-Prospera Clinical Research Pvt. Ltd. The company is currently hiring a Senior CRA (Senior Clinical Research Associate) for its clinical research operations in Maharashtra.
This opening is ideal for candidates with 3–5 years of experience in clinical trials, site monitoring, and clinical research operations who possess strong knowledge of ICH-GCP guidelines, clinical trial management, regulatory compliance, and study documentation practices. Experienced clinical research professionals looking to advance their careers with a research-driven organization can consider this opportunity.
As clinical research and drug development activities continue to expand across India, demand for skilled Clinical Research Associates remains strong. Organizations conducting clinical studies require experienced professionals capable of ensuring protocol compliance, patient safety, data quality, and regulatory adherence throughout the study lifecycle.
Company Overview
Bio-Prospera Clinical Research Pvt. Ltd. is a clinical research organization focused on supporting high-quality research activities and advancing healthcare innovation. The organization works toward improving clinical development processes while maintaining strong standards for quality, compliance, and scientific integrity.
Clinical research plays a critical role in bringing safe and effective therapies to patients. Companies operating in this space require professionals with expertise in site monitoring, regulatory compliance, clinical operations, and Good Clinical Practice (GCP) standards.
Bio-Prospera emphasizes innovation, professional growth, and a collaborative research environment that supports career development for clinical research professionals.
Job Role & Responsibilities
Position: Senior Clinical Research Associate (Senior CRA)
The selected candidate will support clinical trial activities and ensure study execution aligns with regulatory requirements, sponsor expectations, and approved protocols.
Key Responsibilities
- Conduct site monitoring visits for assigned clinical studies.
- Ensure compliance with ICH-GCP guidelines and study protocols.
- Monitor clinical trial progress and site performance.
- Review study documentation for completeness and accuracy.
- Verify source data and ensure data integrity.
- Coordinate with investigators, site staff, sponsors, and project teams.
- Support regulatory submissions and study documentation processes.
- Identify protocol deviations and assist with corrective actions.
- Ensure patient safety and ethical conduct throughout clinical trials.
- Prepare monitoring reports and maintain study records.
- Participate in site initiation, monitoring, and close-out activities.
- Assist in maintaining audit readiness and inspection preparedness.
Skills Expected
The organization is seeking candidates with experience in:
- Clinical Trial Monitoring
- Site Monitoring
- Clinical Operations
- Clinical Trial Management
- ICH-GCP Guidelines
- Regulatory Compliance
- Study Documentation
- Clinical Data Verification
- Quality Management
- Investigator Site Coordination
These competencies are highly valued across CROs, pharmaceutical companies, biotechnology organizations, and healthcare research institutions.
Eligibility / Qualifications
Educational Qualifications
Candidates from the following backgrounds may be suitable:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Microbiology
- Biochemistry
- Clinical Research
- Pharmaceutical Sciences
- Allied Health Sciences
Experience Required
- 3 to 5 years of experience in Clinical Research.
- Experience in Clinical Trials and Site Monitoring.
- Prior CRA experience preferred.
Required Competencies
- Strong knowledge of Good Clinical Practice (GCP) Guidelines.
- Excellent communication skills.
- Strong documentation and reporting abilities.
- Attention to detail and analytical thinking.
- Ability to work independently and collaboratively.
- Understanding of clinical trial regulations and quality systems.
Candidates with experience working on multicenter studies, regulatory audits, and monitoring activities may have an added advantage during the selection process.
Why Consider This Opportunity?
Clinical Research Associates remain among the most in-demand professionals within the pharmaceutical, biotechnology, and healthcare research sectors. With increasing investments in clinical development and drug discovery, experienced CRAs continue to play a critical role in ensuring successful trial execution.
Benefits of pursuing this opportunity include:
- Exposure to diverse clinical research projects.
- Career growth within a specialized clinical research organization.
- Opportunity to work with experienced research professionals.
- Hands-on involvement in clinical trial monitoring activities.
- Professional development in regulatory and quality compliance.
- Long-term career prospects within the CRO industry.
The position is particularly suitable for professionals aiming to strengthen expertise in clinical operations, study monitoring, pharmacovigilance collaboration, quality management systems, and regulatory affairs.
Location & Salary
Location: Vasai East, Mumbai, Maharashtra
Work Mode: On-Site
Experience Required: 3–5 Years
Industry: Clinical Research / CRO
Estimated Salary: Approximately ₹5.5 LPA – ₹9 LPA (based on experience, study exposure, therapeutic area expertise, and organizational policies)
Application Process
Interested and eligible candidates can apply by sending their updated CV to the official email address provided by the company.
Email Application
Email: bd2@bpclinical.com
Candidates should ensure that their resume clearly highlights:
- Clinical trial experience
- Site monitoring exposure
- Therapeutic area expertise
- GCP training and certifications
- Clinical research achievements
- Documentation and compliance experience
Company Address
Bio-Prospera Clinical Research Pvt. Ltd.
Viraj Industrial Estate, Plot No. 44
Dewan and Shah Udyog Nagar
Chinchpada, Vasai East
Mumbai, Maharashtra – 401208
Frequently Asked Questions
What position is Bio-Prospera hiring for?
The company is hiring for the role of Senior Clinical Research Associate (Senior CRA).
How much experience is required?
Candidates should have 3–5 years of experience in clinical trials and clinical research monitoring.
Is GCP knowledge mandatory?
Yes. Strong understanding of Good Clinical Practice (GCP) guidelines is one of the key requirements.
What educational qualifications are preferred?
Candidates with qualifications such as B.Pharm, M.Pharm, Pharm.D, Biotechnology, Life Sciences, Microbiology, and related fields can apply.
What are the major responsibilities of this role?
The position involves site monitoring, clinical trial oversight, documentation review, protocol compliance, and regulatory support.
How can candidates apply?
Applicants can send their updated CV directly to bd2@bpclinical.com.
Summary
| Category | Details |
|---|---|
| Company | Bio-Prospera Clinical Research Pvt. Ltd. |
| Department Vacancies | Senior Clinical Research Associate (Senior CRA) |
| Qualification | B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc Life Sciences, Biotechnology, Microbiology, Clinical Research |
| Experience | 3–5 Years |
| Location | Vasai East, Mumbai, Maharashtra |
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