"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs"

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"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs" (Syneos Health Hiring Safety & PV Coordinator in Hyderabad) Introduction Candidates looking to build a strong and long-term career in Pharmacovigilance (PV) and Drug Safety have an excellent opportunity at Syneos Health , a globally recognized biopharmaceutical solutions organization. Syneos Health is currently hiring for the position of Safety & PV Coordinator at its Hyderabad office . This is a full-time, office-based role , ideal for professionals who have experience or exposure in pharmacovigilance submissions, safety reporting, regulatory compliance, and clinical research processes . Working with a global organization like Syneos Health provides exposure to international safety regulations, cross-functional teams, and structured career growth . About The Company – Syneos Health Syneos Health® is a fully integrated biopharmaceutical solutions organization that supports pha...

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"Senior Clinical Data Associate Job in Ahmedabad – Advanced Clinical Hiring | Apply Now"

"Advanced Clinical Hiring Senior Clinical Data Associate in Ahmedabad – 2025-26 Fast Apply Now"



(Senior Clinical Data Associate Job in Ahmedabad)



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.


About Advanced Clinical:-

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.


Position Overview: Senior Clinical Data Associate:-

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.


Key Responsibilities (Detailed Breakdown):-

Below are the major responsibilities of the Senior Clinical Data Associate role at Advanced Clinical:

1. Advanced-Level Data Review

  • 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

2. Start-up Document Creation

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.

3. User Acceptance Testing (UAT)

  • Perform UAT for EDC systems

  • Validate edit checks, forms, and integrations

  • Ensure database readiness before study go-live

4. EDC System & Module Oversight

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

5. Vendor Data Reconciliation

  • Reconcile Serious Adverse Events (SAEs) from safety databases

  • Reconcile external vendor data such as labs, ECG, and imaging

  • Identify discrepancies and ensure timely resolution

6. Query Management

  • Generate queries for inconsistent data

  • Issue re-queries when needed

  • Communicate discrepancies to investigators and data managers

7. Study Metrics & Account Management

  • Track study progress

  • Maintain EDC user accounts

  • Support documentation for study audits

8. Compliance & Quality Control

  • 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.


Eligibility & Qualifications:-

To apply for this position, you must meet the following qualifications:

Experience

  • 3 years of experience in Clinical Data Management

  • Experience in CRO or the pharmaceutical industry preferred

Education

  • Bachelor’s degree preferred

  • Candidates with strong experience may be considered even without a degree

Skills Required

  • 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.


Why Join Advanced Clinical?

Joining Advanced Clinical offers many benefits, especially for professionals aiming to grow in the CDM domain.

1. International Exposure

Work on global studies involving top pharma and biotech clients.

2. Growth-Focused Environment

The company is known for:

  • Career progression

  • Skill development

  • Continuous training opportunities

3. Diverse & Inclusive Culture

Advanced Clinical provides:

  • Equal opportunities

  • Supportive leadership

  • Healthy work-life balance

  • Collaboration with international teams

4. Strong Industry Reputation

The organisation is known for quality and compliance, which boosts your long-term career credibility.


Job Location:-

Ahmedabad, Gujarat, India
On-site role

The Ahmedabad office provides a professional work environment with exposure to global teams and advanced systems.


Salary (Industry Estimate):-

Based on current market data for Senior CDM roles in India:

₹6,00,000 – ₹10,00,000 per annum

Final salary depends on:

  • Total experience

  • Skill level

  • Interview performance

  • Experience with EDC & CDASH


How to Apply:-

Click the official job link below:

๐Ÿ‘‰ 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


Conclusion:-

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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