Amgen is hiring for the position of Data Management Sr Associate in Hyderabad, Telangana. The role falls under the Clinical Development career category and is offered as a full-time, on-site position.
The selected professional will support clinical trial data management activities throughout the study lifecycle. Key responsibilities include database build testing, data cleaning, query management, reconciliation, database lock preparation, EDC and non-CRF data setup, timeline tracking, and coordination with internal and external clinical research teams.
Candidates with a relevant academic background and experience in clinical execution, life sciences, clinical research, or clinical data management may be eligible.
Amgen Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Amgen |
| Position | Data Management Sr Associate |
| Career Category | Clinical Development |
| Job Location | Hyderabad, Telangana |
| Work Mode | On Site |
| Employment Type | Full Time |
| Job Requisition ID | R-255251 |
| Qualification | Master’s / Bachelor’s / Associate’s / High School + Relevant Experience |
| Preferred Experience | 3 Years Life Sciences/Medical Field; including 1 Year Biopharma Clinical Research |
| Function | Clinical Data Management |
| Salary/CTC | Not Disclosed for India |
About Amgen
Amgen is a biotechnology company involved in the development and delivery of medicines for serious diseases. The company conducts research and development across therapeutic areas including Oncology, Inflammation, General Medicine, and Rare Disease.
The Data Management team supports clinical development by ensuring that clinical trial data is collected, reviewed, cleaned, reconciled, and prepared for analysis according to applicable quality and compliance requirements.
Amgen Data Management Sr Associate Job Description
The Data Management Sr Associate will contribute to the delivery of high-quality clinical trial data by performing core data management activities across the study lifecycle.
The position requires the candidate to work with clinical data structures, electronic data capture systems, queries, data reconciliation, and study timelines while coordinating with global teams and external partners when required.
Sr Data Management Support
The selected candidate will perform data management activities with limited supervision and take ownership of time-sensitive deliverables.
The role requires attention to data quality, timelines, documentation, compliance, and effective collaboration across clinical research functions.
Educational Qualification
Amgen provides multiple qualification pathways for this position:
- Master’s degree, or
- Bachelor’s degree with 2 years of clinical execution experience, or
- Associate’s degree with 6 years of clinical execution experience, or
- High school diploma/GED with 8 years of clinical execution experience
The company also lists relevant experience in life sciences or medically related fields as a preferred qualification.
Experience Requirements
Preferred candidates should have approximately 3 years of work experience in a life sciences or medically related field.
This should include approximately 1 year of biopharmaceutical clinical research experience gained while working on clinical trials within a:
- Biotechnology company
- Pharmaceutical company
- Contract Research Organization (CRO)
Experience working in Data Management for global clinical trials is also preferred.
Clinical Data Management Skills
The position requires knowledge and practical ability in areas such as:
- Clinical data management
- Database build testing
- Data cleaning
- Query management
- Data reconciliation
- Database lock preparation
- EDC data structures
- Non-CRF data structures
- Local laboratory data
- Coding dictionaries
- Non-CRF data integrations
- Clinical study timelines
- Data management deliverables
- Risk identification and escalation
Key Responsibilities
1. Clinical Data Management Activities
- Execute assigned clinical data management activities throughout the study lifecycle.
- Support database build testing.
- Perform clinical data cleaning activities.
- Manage and follow up on data queries.
- Conduct data reconciliation.
- Support preparation activities for database lock.
- Complete assigned deliverables with limited supervision.
2. EDC and Non-CRF Data Management
- Support the setup and maintenance of EDC data structures.
- Work with non-CRF data structures.
- Support local laboratory data setup.
- Work with coding dictionaries.
- Contribute to non-CRF data integrations.
- Help maintain data structures required for effective clinical trial execution.
3. Support Data Management Functions
The role will support core Data Management functions such as:
- Data Delivery Leads
- Database Designers
- Data Acquisition Leads
The selected candidate will take ownership of time-sensitive activities and ensure deliverables are completed accurately and within agreed timelines.
4. Study Timeline and Risk Management
- Monitor progress against data management timelines.
- Track study-level timelines and deliverables.
- Identify potential delays and operational risks.
- Escalate issues appropriately.
- Maintain clear documentation of identified risks.
- Support development or implementation of mitigation activities where required.
5. Cross-Functional Collaboration
- Coordinate with local internal teams.
- Work with global clinical research team members.
- Collaborate with external partners and Functional Service Providers (FSPs) when required.
- Ensure alignment across teams involved in clinical study activities.
- Support efficient and timely delivery of study-related work.
6. Process Improvement
- Identify opportunities to improve repeatable data management processes.
- Contribute to standardization and best practices.
- Share knowledge and relevant learnings with team members.
- Support continuous improvement initiatives within the Data Management function.
Preferred Qualifications
The following experience and qualifications are preferred:
- Around 3 years of experience in life sciences or a medically related field.
- At least 1 year of biopharmaceutical clinical research experience.
- Clinical trial experience in a biotechnology, pharmaceutical, or CRO environment.
- Experience supporting global clinical trials.
- Practical exposure to clinical data management activities.
Work Location and Work Environment
The position is based in Hyderabad, Telangana, India.
The vacancy specifies the work arrangement as On Site, so candidates should be prepared to work from the Hyderabad location.
The source does not specify particular shift timings.
Salary / CTC
The available job posting does not provide an India-specific salary or CTC for the Data Management Sr Associate position.
The posting includes a U.S. annual base salary section, but that information is not applicable as an advertised salary range for the Hyderabad position.
Candidates should confirm the compensation package applicable to the India role during the recruitment process.
Benefits and Career Development
Amgen states that eligible employees may receive benefits and opportunities related to professional development and well-being. The benefits described in the source include:
- Employee health and welfare benefits
- Medical, dental, and vision coverage
- Life and disability insurance
- Retirement and savings opportunities
- Flexible spending arrangements
- Discretionary annual bonus program, subject to eligibility
- Stock-based long-term incentives
- Time-off programs
- Career development opportunities
- Flexible work models where applicable
Eligibility and availability of individual benefits can vary by location, employment terms, and applicable company policies.
Selection Process
The source vacancy does not provide a detailed selection process.
Candidates should refer to Amgen’s recruitment communication for information about screening, interviews, assessments, or other stages of the hiring process.
How to Apply
Interested and eligible candidates can apply through the official Amgen Careers application page.
Candidates should ensure their resume clearly highlights experience in clinical research, clinical execution, data management, clinical trials, EDC, data cleaning, query management, and reconciliation, wherever applicable.
Important Details Before Applying
- Position: Data Management Sr Associate
- Company: Amgen
- Location: Hyderabad, Telangana
- Work mode: On Site
- Employment: Full Time
- Career category: Clinical Development
- Requisition ID: R-255251
- Multiple education and experience pathways are accepted.
- Preferred background includes life sciences or a medically related field.
- Biopharmaceutical clinical research experience is preferred.
- Global clinical trial data management experience is an advantage.
- Key activities include database testing, data cleaning, queries, reconciliation, and lock preparation.
- Salary/CTC for the India position is not disclosed.
Frequently Asked Questions
1. What position is Amgen hiring for?
Amgen is hiring for a Data Management Sr Associate position.
2. Where is the job located?
The position is based in Hyderabad, Telangana, India.
3. Is this a remote position?
No. The vacancy specifies the work arrangement as On Site.
4. What educational qualifications are accepted?
Amgen lists several pathways, including a Master’s degree, or a Bachelor’s/Associate’s/high-school qualification combined with specified clinical execution experience.
5. Is clinical research experience required?
Relevant clinical execution experience is required for some of the qualification pathways, while biopharmaceutical clinical research experience is specifically listed as preferred.
6. Is clinical data management experience preferred?
Yes. Experience working in Data Management on global clinical trials is specifically listed as a preferred qualification.
7. What are the main responsibilities?
The role covers database build testing, data cleaning, query management, reconciliation, lock preparation, EDC/non-CRF data setup, timeline tracking, risk escalation, and cross-functional coordination.
8. What type of clinical systems or data structures are involved?
The role includes EDC and non-CRF data structures, local laboratory data, coding dictionaries, and non-CRF data integrations.
9. What is the salary for this position?
An India-specific salary or CTC is not disclosed in the available posting.
10. How can candidates apply?
Candidates can apply through the official Amgen Careers application page using the application link provided above.
Important Note
Job responsibilities, eligibility criteria, compensation, benefits, work arrangements, and recruitment conditions may change during the hiring process. Candidates should verify the latest information on the official Amgen Careers page before applying.