Regulatory Affairs Job in Hyderabad at Makro Group for regulatory affairs role. Apply online for pharma research and clinical trial analysis job.
Professionals with experience in regulatory affairs and scientific research now have a strong opportunity to work in a data-driven pharmaceutical research role. A reputed organization is hiring Research Analyst-II for Regulatory Affairs, focusing on secondary research, clinical trial intelligence, and regulatory data analysis. This role is ideal for candidates who enjoy analyzing scientific data and working on global pharma insights.
Company Overview
Makro Group is a global organization offering integrated services across the pharmaceutical and life sciences value chain. The company specializes in research, regulatory consulting, and analytics, helping clients navigate complex challenges in drug development and commercialization. With expertise across multiple domains, Makro Group provides a collaborative environment for professionals to grow in research and regulatory sciences.
Job Overview (Job Details)
| Category | Details |
|---|---|
| Organization | Makro Group |
| Role | Research Analyst-II (Regulatory Affairs) |
| Qualification | Any UG / PG in Life Sciences |
| Experience | 2–4 Years |
| Job Location | Hyderabad |
| Employment Type | Full-Time |
| Application Mode | Online |
| Salary | Not Disclosed |
Job Location & Employment Type
The position is based in Hyderabad and is a full-time role within the Research & Development / Regulatory Affairs domain.
Open Positions / Department Details
The hiring is for the Regulatory Affairs and Research Analytics team. The role focuses on secondary research, regulatory intelligence, and clinical data analysis related to pharmaceutical and biotech products.
Key Roles & Responsibilities
Candidates selected for this role will be responsible for:
- Conducting secondary research to develop detailed product and company profiles
- Analyzing regulatory frameworks and guidelines across global markets
- Collecting and interpreting data from sources such as clinical trial reports, company filings, and scientific publications
- Monitoring developments in drug, device, and biotech research
- Evaluating regulatory impact on product development and approval processes
- Compiling and maintaining scientific and regulatory databases
- Supporting intelligence research on pharma companies and R&D pipelines
- Mentoring junior team members and ensuring data quality
Eligibility Criteria
Education
- Any Undergraduate or Postgraduate degree in Life Sciences
Experience
- 2–4 years of relevant experience in regulatory affairs or research
- Strong exposure to secondary research and clinical trial data
Skills Required
- Strong knowledge of Regulatory Affairs and product development lifecycle
- Understanding of clinical trials, drug development, and regulatory approvals
- Excellent secondary research and data analysis skills
- Familiarity with scientific terminology and regulatory guidelines
- Ability to interpret complex scientific and regulatory data
- Strong analytical and problem-solving skills
Additional Skills
- Knowledge of global regulatory bodies and compliance standards
- Experience with research databases and scientific sources
- Ability to manage multiple projects and deadlines
- Good communication and reporting skills
Salary & Benefits
- Salary: Not disclosed (as per company standards)
- Opportunity to work on global pharma and biotech research projects
- Exposure to regulatory intelligence and clinical data analysis
- Career growth in regulatory affairs and research domains
- Professional and collaborative work environment
Selection Process
The hiring process generally includes:
- Online Application
- Resume Screening
- Technical / Research-Based Interview
- HR Discussion
- Final Selection
How to Apply
Interested candidates can apply through the official company career portal. Ensure your resume highlights your experience in regulatory affairs, clinical research, and data analysis.
Important Dates
- Last Date to Apply: Not specified
Why Apply for This Pharma Job?
This role offers a unique opportunity to work at the intersection of regulatory affairs, research analytics, and clinical intelligence. Candidates will gain valuable experience in analyzing global pharmaceutical trends and regulatory frameworks.
It is an ideal career path for professionals interested in regulatory consulting, market intelligence, and data-driven decision-making in the life sciences industry.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with any recruiter or company. We do not charge any fee for job applications. Candidates should verify all details independently before applying.
Final Call-to-Action
If you have experience in regulatory affairs and enjoy research-driven roles, this is a great opportunity to advance your career. Apply now and grow in the field of regulatory intelligence and pharma research.
