Axis Clinicals Ltd, a leading global Clinical Research Organization (CRO), is conducting a Walk-In Drive for Trainee Research Associate positions at its Miyapur, Hyderabad facility. This opportunity is ideal for B.Pharm, M.Pharm, and Pharm.D freshers seeking careers in Clinical Research, Quality Assurance (QA), and Medical Writing.
With growing demand in BA/BE studies and regulatory documentation, this Trainee Research Associate role offers structured exposure to clinical trial documentation, SOP management, IRB/IEC submissions, and bioanalytical QA review.
📍 Walk-In Details
- Company: Axis Clinicals
- Role: Trainee Research Associate (QA & Medical Writer)
- Experience: 0–1 Years (Freshers Eligible)
- Salary: ₹1.75 – ₹2.25 LPA
- Location: Miyapur, Hyderabad
- Walk-In Date: 18th & 19th February
- Time: 10:00 AM – 1:00 PM
- Venue: Axis Clinicals Ltd, 1-121/1, Miyapur – 500049
- Contact: Rohitha
- Commitment: 2 Years
Job Overview – Trainee Research Associate
The Trainee Research Associate position at Axis Clinicals is divided into two functional tracks:
- Medical Writing
- Quality Assurance (Clinical & Bioanalytical)
This Clinical Research job in Hyderabad provides foundational exposure to BA/BE studies, regulatory submissions, SOP compliance, and audit processes.
Key Responsibilities
🔬 Medical Writing Responsibilities
- Conducting literature surveys for study planning
- Preparing protocol summaries based on sponsor requirements
- Drafting study protocols and informed consent documents (ICFs)
- Managing IRB/IEC submissions and coordination
- Supporting regulatory documentation for clinical trials
🧪 Research Associate – Quality Assurance Responsibilities
- Generation, distribution, archival of SOPs and logbooks
- Issuing controlled forms and maintaining master SOP lists
- Coordinating employee training and personnel file maintenance
- Conducting facility and system audits
- Auditing IRB/IEC, vendors, and third-party service providers
- Reviewing:
- Study protocols and ICFs
- Clinical raw data and reports
- Bioanalytical validation data & chromatograms
- Biostatistics and summary reports
- Software validations & IQ/OQ/PQ documentation
- Compilation of regulatory documents
- Archiving study reports per SOP compliance
This makes the role highly suitable for candidates aiming to build careers in Clinical QA, Regulatory Affairs, Medical Writing, or Bioanalytical Quality Review.
Eligibility Criteria
- Qualification: B.Pharm / M.Pharm / Pharm.D
- Experience: 0–1 year (Freshers Preferred)
- Strong knowledge of:
- Clinical research documentation
- SOP management
- Regulatory guidelines
- BA/BE studies
- eCTD basics (preferred)
- Willingness to commit for 2 years
Why Join Axis Clinicals?
Axis Clinicals is a globally recognized CRO:
- Operational since 2006
- Headquarters in Hyderabad
- Facilities in India, US & Mexico
- 700+ clinical research professionals
Benefits include:
- Hands-on exposure to clinical trial QA and medical writing
- Strong regulatory documentation experience
- Direct interaction with IRB/IEC processes
- Career pathway into Clinical Research, QA, PV, and Regulatory Affairs
How to Apply?
Eligible candidates can attend the walk-in interview directly at the Miyapur facility on 18th or 19th February between 10:00 AM and 1:00 PM.