Join Croissance Clinical Research, a fast-growing Clinical Research Organization (CRO) based in Hyderabad, Telangana, dedicated to advancing clinical trials with innovation and excellence. With a focus on delivering high-quality clinical research services to pharmaceutical and biotech companies, Croissance supports global trials adhering to ICH-GCP and regulatory standards.

We’re hiring experienced professionals for Clinical Data Manager, Clinical Research Associate (CRA), and QA-Executive roles to strengthen our team and drive impactful healthcare solutions.

Recruitment Details: Ongoing Hiring

This recruitment drive seeks experienced candidates for roles based in Hyderabad, supporting clinical trials for global sponsors. Candidates should have relevant experience in clinical research or CRO environments.

Job Location

Croissance Clinical Research, Hyderabad, Telangana (specific address not disclosed; contact HR for details)

Job Opportunities at Croissance Clinical Research

We’re hiring for Clinical Data Manager, Clinical Research Associate (CRA), and QA-Executive roles to support clinical trial operations, data management, and quality assurance. All positions require experience in regulated environments, preferably with exposure to USFDA, EMA, or ICH-GCP standards.

1. Clinical Data Manager

Position: Clinical Data Manager
Qualification: B.Pharm, M.Pharm, M.Sc. (Life Sciences, Biotechnology), or equivalent
Experience: 5-7 years in clinical data management
Key Responsibilities:
- Oversee end-to-end clinical data management processes, from CRF design to database lock
- Develop and implement Data Management Plans (DMPs) and ensure data quality
- Perform data cleaning, query resolution, and validation using EDC systems (e.g., Medidata, Oracle Clinical)
- Coordinate with biostatisticians and clinical teams for data analysis and reporting
- Ensure compliance with ICH-GCP, 21CFR Part 11, and sponsor requirements
Key Skills:
- Proficiency in EDC platforms (Medidata Rave, Oracle InForm)
- Expertise in CDISC standards (SDTM, ADaM) and data validation
- Knowledge of GCP, GCDMP, and regulatory guidelines
- Strong analytical and problem-solving skills
- Experience with data reconciliation and audit readiness
Openings: Multiple (likely 2-3 based on CRO hiring trends)
Salary: ₹6.0–12.0 Lakhs/year (estimated based on industry standards for Hyderabad)

2. Clinical Research Associate (CRA)

Position: Clinical Research Associate
Qualification: B.Pharm, M.Pharm, M.Sc. (Life Sciences, Biotechnology), or equivalent
Experience: 4-5 years in clinical trial monitoring
Key Responsibilities:
- Conduct site initiation, monitoring, and close-out visits for Phase I-IV trials
- Ensure adherence to protocol, ICH-GCP, and regulatory requirements (USFDA, EMA)
- Verify source data, CRFs, and informed consent documents
- Manage site queries, report adverse events, and ensure data integrity
- Collaborate with investigators and sponsors to meet trial timelines
Key Skills:
- Expertise in clinical trial monitoring and site management
- Knowledge of ICH-GCP, cGMP, and local regulations
- Proficiency in CTMS and eTMF systems
- Strong communication and interpersonal skills
- Ability to travel for on-site monitoring
Openings: Multiple (likely 3-4 based on trial demands)
Salary: ₹5.0–9.0 Lakhs/year (estimated based on industry standards)

3. QA-Executive

Position: QA-Executive
Qualification: B.Pharm, M.Pharm, M.Sc. (Chemistry, Life Sciences), or equivalent
Experience: 3-4 years in quality assurance for clinical research
Key Responsibilities:
- Develop and implement QA processes for clinical trials per ICH-GCP
- Conduct internal audits of trial processes, TMFs, and data management systems
- Review SOPs, protocols, and study reports for compliance
- Support regulatory inspections (USFDA, EMA) and sponsor audits
- Manage CAPA, deviations, and risk assessments to ensure quality
Key Skills:
- Expertise in GCP, QMS, and audit processes
- Knowledge of regulatory guidelines (USFDA, EMA, CDSCO)
- Proficiency in TMF management and audit documentation
- Strong attention to detail and risk management skills
- Experience with CAPA and deviation handling
Openings: Multiple (likely 2-3 based on QA needs)
Salary: ₹4.0–7.0 Lakhs/year (estimated based on industry standards)

Why Join Croissance Clinical Research?

Croissance Clinical Research, a Hyderabad-based CRO, is recognized for its innovative approach to clinical trials, supporting pharmaceutical and biotech sponsors globally. Rated approximately 3.5/5 on Glassdoor for work culture, employees praise the learning opportunities and exposure to global trials but note challenges with work-life balance due to tight project timelines. With a focus on oncology, cardiology, and rare diseases, Croissance offers a platform to work on cutting-edge research in a dynamic environment.

Key Benefits

Contribute to global clinical trials in a USFDA/EMA-compliant CRO
Gain expertise in EDC, CTMS, and QMS systems
Work on innovative therapies in oncology and rare diseases
Join a growing organization in Hyderabad’s biotech hub
Access career advancement through hands-on trial experience

How to Apply

Send your CV to hr@croissancecr.com with the subject “Role Name – Hyderabad”. Include:

Updated resume
Educational certificates (B.Pharm, M.Pharm, M.Sc.)
Experience letters and last 3 months’ payslips
Aadhar and PAN cards
Preparation:
- Clinical Data Manager: Review EDC systems, CDISC, and data validation
- CRA: Study ICH-GCP, site monitoring, and CTMS
- QA-Executive: Prepare for QMS, audits, and CAPA processes
- Be ready to discuss regulatory exposure and trial experience
Note: Croissance Clinical Research does not charge recruitment fees; verify communications via @croissancecr.com emails. For queries, contact HR at hr@croissancecr.com. Apply promptly to secure an interview slot.

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Croissance Clinical Research Hiring for Clinical Data Manager, Clinical Research Associate, and QA-Executive Roles

About Croissance Clinical Research

Croissance Clinical Research, established in Hyderabad, provides end-to-end clinical research services, including data management, monitoring, and quality assurance for Phase I-IV trials. With a team of skilled professionals and a focus on clinical innovation, we partner with global sponsors to deliver high-quality trial outcomes. Our commitment to ICH-GCP and data integrity ensures trust and reliability in clinical research.

Our Mission

Drive excellence in clinical research
Deliver reliable, high-quality trial data
Foster a collaborative, innovative workplace

Apply now by emailing hr@croissancecr.com. Join Croissance Clinical Research in Hyderabad and advance global healthcare through clinical innovation!