OrciMed Hiring Senior Clinical Data Manager; Database Programmer; Medical Coding Specialist
- Company Overview
- Job Role & Responsibilities
- Senior Clinical Data Managers
- Database Programmers
- Medical Coding Specialists
- Eligibility / Qualifications
- Location & Shift Details
- Application Process
- Why Clinical Data Management Is a High-Growth Career
- Career Growth Opportunities
- Frequently Asked Questions (FAQs)
- 1. Is this a remote opportunity?
- 2. What shift is required?
- 3. Are freshers eligible?
- 4. Which EDC systems are preferred?
- 5. How do I apply?
- Job Summary
CDM & Coding Vacancies in Hyderabad
5+ yrs CDM, 2+ yrs DB Programming & Medical Coding vacancies in Hyderabad (UK Shift) at OrciMed Life Sciences.
OrciMed Life Sciences is expanding its global clinical research operations and hiring experienced Clinical Research Professionals for its Hyderabad office. This office-based opportunity is aligned with UK shift hours and is ideal for candidates with proven expertise in Clinical Data Management (CDM), Database Programming, and Medical Coding. Immediate joiners are preferred.
If you are seeking high-growth clinical research jobs in Hyderabad with exposure to global trials, electronic data capture (EDC) systems, and regulatory-compliant clinical database environments, this hiring drive presents a strong career opportunity.
Company Overview
OrciMed Life Sciences operates in the clinical research and data management space, supporting pharmaceutical, biotechnology, and life sciences organizations with trial data oversight and regulatory-aligned database management services.
Clinical data management plays a critical role in ensuring the accuracy, integrity, and compliance of clinical trial data submitted to regulatory authorities such as the USFDA, EMA, and MHRA. Organizations in this sector must maintain strict adherence to GCP (Good Clinical Practice), 21 CFR Part 11 compliance, and global data governance standards.
Working at OrciMed provides exposure to:
- End-to-end Clinical Data Management processes
- Electronic Data Capture (EDC) platforms
- Clinical database build and validation
- Medical coding using global dictionaries
- Regulatory-compliant clinical documentation systems
As global clinical trials increase in complexity, demand for skilled clinical data managers, database programmers, and medical coding specialists continues to rise.
Job Role & Responsibilities
OrciMed is hiring across three specialized clinical research functions:
Senior Clinical Data Managers
Experience: 5+ Years
Location: Hyderabad (Office-Based)
Shift: UK Shift Hours
Key Responsibilities:
- Managing end-to-end Clinical Data Management (CDM) activities
- Overseeing database design, validation, and data cleaning processes
- Coordinating with biostatistics and clinical operations teams
- Ensuring compliance with GCP and regulatory guidelines
- Managing data review cycles and query resolution workflows
- Supporting database lock and submission readiness
Required Expertise:
- Strong experience in Electronic Data Capture (EDC) systems
- Exposure to Clinical One or Viedoc preferred
- Hands-on understanding of clinical trial lifecycle management
Senior CDMs are responsible for maintaining data integrity across global clinical trials. This is a high-responsibility role directly impacting regulatory submissions and trial outcomes.
Database Programmers
Experience: 2+ Years
Location: Hyderabad (Office-Based)
Shift: UK Shift Hours
Key Responsibilities:
- Building and programming clinical trial databases
- Configuring EDC systems such as Clinical One and/or Viedoc
- Performing database validation and UAT support
- Implementing edit checks and validation rules
- Supporting mid-study updates and system enhancements
Required Expertise:
- Strong database build experience
- Hands-on programming within EDC platforms
- Understanding of clinical protocol requirements
Database Programmers ensure that clinical trial data is captured accurately and in compliance with regulatory frameworks.
Medical Coding Specialists
Experience: 2+ Years
Location: Hyderabad (Office-Based)
Shift: UK Shift Hours
Key Responsibilities:
- Performing medical coding using MedDRA and WHODrug dictionaries
- Utilizing integrated coding tools within EDC systems
- Ensuring accuracy in adverse event and medication coding
- Collaborating with data management teams for query resolution
Preferred Experience:
- Experience with Clinical One or Viedoc
- Exposure to global clinical trial coding standards
Medical Coding Specialists play a key role in ensuring standardized terminology alignment for regulatory submissions and pharmacovigilance reporting.
Eligibility / Qualifications
Educational Qualifications (comma-separated):
B.Pharm, M.Pharm, Pharm.D, B.Sc Life Sciences, M.Sc Life Sciences, Biotechnology, Clinical Research, Biostatistics
Experience Requirements:
- Senior Clinical Data Managers: 5+ years in CDM
- Database Programmers: 2+ years in clinical database programming
- Medical Coding Specialists: 2+ years in MedDRA/WHODrug coding
Mandatory Skills:
- Experience with Electronic Data Capture (EDC) systems
- Knowledge of GCP and regulatory compliance standards
- Strong analytical and documentation skills
Candidates without relevant clinical research or EDC experience may not meet the selection criteria.
Location & Shift Details
Location: Hyderabad (Office-Based)
Shift: UK Shift Hours
Working in UK shift supports collaboration with global sponsors and international clinical trial teams. Hyderabad continues to be a leading hub for clinical research, pharmacovigilance, and life sciences data management operations.
Salary will depend on role, expertise, and years of experience. Clinical Data Management and Medical Coding are considered high-demand, high-value career domains due to regulatory complexity and global trial expansion.
Application Process
Interested candidates should send their updated CV to:
Email: Careers@orcimedlifesciences.com
Application Steps:
- Update your resume highlighting EDC, CDM, database programming, or coding expertise.
- Mention specific systems used (Clinical One, Viedoc, MedDRA, WHODrug).
- Indicate availability for UK shift.
- Email your CV to the HR contact provided.
Immediate joiners will be given preference.
Why Clinical Data Management Is a High-Growth Career
Clinical Data Management and medical coding roles are central to regulatory submissions, pharmacovigilance reporting, and global trial transparency. Without clean and validated data, clinical trials cannot progress to drug approval stages.
Professionals in this domain gain expertise in:
- Regulatory-compliant data handling
- Electronic data capture platforms
- Global dictionary coding systems
- Cross-functional collaboration with biostatistics and clinical operations
As global clinical research investments increase, experienced CDM professionals and database programmers remain in high demand.
Career Growth Opportunities
Professionals joining OrciMed may progress toward roles such as:
- Lead Clinical Data Manager
- Clinical Data Management Manager
- EDC Systems Specialist
- Clinical Database Architect
- Global Medical Coding Lead
- Clinical Operations Manager
Strong EDC platform expertise and regulatory knowledge significantly improve long-term compensation potential in the clinical research industry.
Frequently Asked Questions (FAQs)
1. Is this a remote opportunity?
No. The role is office-based in Hyderabad.
2. What shift is required?
UK shift hours.
3. Are freshers eligible?
No. Relevant experience is mandatory for all positions.
4. Which EDC systems are preferred?
Clinical One and Viedoc experience is preferred.
5. How do I apply?
Send your CV to Careers@orcimedlifesciences.com.
Job Summary
| Company | OrciMed Life Sciences |
|---|---|
| Vacancies | Senior Clinical Data Manager; Database Programmer; Medical Coding Specialist |
| Required Education | B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences |
| Experience | 5+ Years (CDM); 2+ Years (DB Programming & Coding) |
To apply for this job email your details to Careers@orcimedlifesciences.com
