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If you’re aiming to build a strong and rewarding career in Clinical Data Management, this new opening from Advanced Clinical could be the perfect opportunity for you.
Advanced Clinical is a well-known global clinical development organisation committed to providing high-quality, patient-centred research solutions. With a strong reputation in the global pharma and biotech industry, the company is expanding its India operations and is now hiring an experienced Senior Clinical Data Associate in Ahmedabad.
Advanced Clinical is an international Clinical Research Organisation (CRO) offering full-service clinical development, biometrics, and strategic resourcing services. The company works with global pharmaceutical, biotech, and medical device organisations to deliver safe and effective clinical trials.
Some highlights of the organisation:
Global presence across North America, Europe, and Asia
Focused on quality, compliance, and patient safety
Known for innovative clinical operations and data management
Employee-centric culture with opportunities for career growth
For clinical data professionals, Advanced Clinical provides exposure to global studies and modern data management systems.
The Senior Clinical Data Associate (SCDA) plays a vital role in ensuring accuracy, completeness, and compliance of clinical trial data. This role involves advanced-level data review, data validation, EDC oversight, and vendor reconciliation.
You will collaborate closely with the data management team, clinical operations team, external vendors, and stakeholders to ensure that all study data meets high regulatory and quality standards.
This position is on-site in Ahmedabad, making it a great opportunity for professionals looking to work in a corporate, structured environment within the pharma/CRO sector.
Below are the major responsibilities of the Senior Clinical Data Associate role at Advanced Clinical:
Review clinical trial data for accuracy and completeness
Identify inconsistencies in eCRFs (Electronic Case Report Forms)
Perform manual data review and listing review
Issue queries and manage query resolution
Ensure data follows study guidelines and CDASH standards
You will assist the Lead Data Manager in preparing several key documents, such as:
Data Management Plan (DMP)
Edit Check Specifications (ECS)
eCCG guidelines
Study start-up documentation
These documents help form the foundation of the clinical database for each study.
Perform UAT for EDC systems
Validate edit checks, forms, and integrations
Ensure database readiness before study go-live
You will support integration and maintenance of multiple electronic systems, including:
EDC (Electronic Data Capture)
ePRO (Electronic Patient-Reported Outcomes)
IVRS/IWRS (Randomisation & Trial Supply Management)
Investigational product dispensing systems
Reconcile Serious Adverse Events (SAEs) from safety databases
Reconcile external vendor data such as labs, ECG, and imaging
Identify discrepancies and ensure timely resolution
Generate queries for inconsistent data
Issue re-queries when needed
Communicate discrepancies to investigators and data managers
Track study progress
Maintain EDC user accounts
Support documentation for study audits
Follow company SOPs, regulatory standards, and protocol requirements
Perform QC review of data and documents
Ensure inspection-readiness of the study database
Support the archival of study data once trials are completed
This role requires strong analytical skills, attention to detail, and the ability to work under tight timelines.
To apply for this position, you must meet the following qualifications:
< 3 years of experience in Clinical Data Management
Experience in CRO or the pharmaceutical industry preferred
Bachelor’s degree preferred
Candidates with strong experience may be considered even without a degree
Deep understanding of CDASH standards
Experience with EDC systems
Strong communication & documentation skills
Ability to identify data trends and inconsistencies
Excellent organisational and analytical abilities
Candidates with hands-on experience in query management, SAE reconciliation, and global clinical trials are preferred.
Joining Advanced Clinical offers many benefits, especially for professionals aiming to grow in the CDM domain.
Work on global studies involving top pharma and biotech clients.
The company is known for:
Career progression
Skill development
Continuous training opportunities
Advanced Clinical provides:
Equal opportunities
Supportive leadership
Healthy work-life balance
Collaboration with international teams
The organisation is known for quality and compliance, which boosts your long-term career credibility.
Ahmedabad, Gujarat, India
On-site role
The Ahmedabad office provides a professional work environment with exposure to global teams and advanced systems.
Based on current market data for Senior CDM roles in India:
Final salary depends on:
Total experience
Skill level
Interview performance
Experience with EDC & CDASH
Click the official job link below:
๐ Apply Here
https://careers.advancedclinical.com/jobs/840/senior-clinical-data-associate
Make sure your resume highlights:
EDC systems used
Study types handled
CDASH experience
Query management
Vendor reconciliation experience
If you have strong experience in Clinical Data Management and are looking to grow into a senior-level role, then this opportunity with Advanced Clinical is a perfect match.
The role offers hands-on responsibilities, exposure to global clinical trials, and a supportive organisational culture that values quality and innovation.
Apply today to take the next major step in your clinical data management career!
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