Home › Clinical Data Management (CDM) › Medpace Hiring for Clinical Data & Database Roles in Unit 1203, 12th Floor, Building Q2, Aurum QPark, TTC Industrial Area, Thane Belapur Road, Navi Mumbai (Maharashtra) – 400710
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Medpace Hiring for Clinical Data & Database Roles in Unit 1203, 12th Floor, Building Q2, Aurum QPark, TTC Industrial Area, Thane Belapur Road, Navi Mumbai (Maharashtra) – 400710

MedpaceClinical Data & Database RolesUnit 1203, 12th Floor, Building Q2, Aurum QPark, TTC Industrial Area, Thane Belapur Road, Navi Mumbai (Maharashtra) – 400710

Verified Opening

Official Hiring Directive: Formal recruitment circular released by Medpace for Clinical Data & Database Roles in Unit 1203, 12th Floor, Building Q2, Aurum QPark, TTC Industrial Area, Thane Belapur Road, Navi Mumbai (Maharashtra) – 400710. Candidates meeting the specified qualifications and competencies are advised to submit applications before the scheduled closing date.

Position Overview & Specifications

Parameter Official Specifications
Hiring Organization Medpace
Designation / Role Clinical Data & Database Roles
Functional Department Clinical Research
Work Location Unit 1203, 12th Floor, Building Q2, Aurum QPark, TTC Industrial Area, Thane Belapur Road, Navi Mumbai (Maharashtra) – 400710
Experience Requirement Entry-Level / Freshers Welcomefor Review Associate (Hospital Nursing Experience) •1 – 3+ Yearsfor Programmer, Coder & Designer
Target Qualifications B.Pharm, M.Pharm, M.Sc Statistics, Mathematics, Computer Science, Life Sciences
Application Procedure Direct Official Online Submission / HR Notification

Key Roles & Detailed Responsibilities

  • Execute core operational deliverables for Clinical Data & Database Roles aligned with Medpace’s SOPs and compliance frameworks.
  • Perform scheduled assessments, data verification, laboratory tests, or regulatory reviews as assigned.
  • Maintain audit-compliant documentation and coordinate closely with cross-functional project leads.
  • Adhere strictly to global regulatory mandates (cGMP, GCP, ALCOA+ principles).

Eligibility Criteria & Candidate Profile

  • Educational Qualification: B.Pharm, M.Pharm, M.Sc Statistics, Mathematics, Computer Science, Life Sciences from an accredited university.
  • Experience Level: Entry-Level / Freshers Welcomefor Review Associate (Hospital Nursing Experience) •1 – 3+ Yearsfor Programmer, Coder & Designer in relevant healthcare, pharma, or clinical research environments.
  • Strong domain competencies, documentation precision, and communication capabilities.
  • Demonstrated adherence to quality assurance and standard operating protocols.

Core Technical Competencies & Instruments Matrix

Candidates possessing hands-on proficiency across the following analytical tools, software systems, and regulatory standards will receive priority evaluation:

cGMP & Good Documentation Practices (GDP Standards)Standard Operating Procedure (SOP) Implementation & ControlALCOA+ Data Integrity PrinciplesPharmaceutical Quality System (PQS – ICH Q10 Guidelines)Root Cause Analysis (RCA) & Deviation ReportingCross-Functional Interdepartmental CollaborationEnterprise Resource Planning (ERP / SAP Systems)Microsoft Office Suite (Advanced Excel & Data Analytics)Cleanroom Hygiene, 5S Methodology & EHS ComplianceRegulatory Audit Preparedness & Everyday Inspection Readiness

Daily Operational Workflow & Core Shift Duties

Detailed technical breakdown of standard shift activities, laboratory/plant floor execution, and daily operational deliverables for Clinical Data & Database Roles:

Duty 1Shift Handover & Daily Briefing
Reviewing prior shift logbooks, receiving operational assignments, and verifying workstation readiness.

Duty 2Standard Operating Procedure (SOP) Execution
Carrying out operational duties strictly within approved written SOPs, safety instructions, and cGMP norms.

Duty 3Good Documentation Practice (GDP) Records
Contemporaneously logging observations, process parameters, and activity completions in official logbooks using indelible ink.

Duty 4Workplace Hygiene & 5S Maintenance
Ensuring equipment, tools, and work suites are maintained clean, organized, and properly labeled according to 5S principles.

Duty 5Quality Incident & Anomaly Escalation
Promptly stopping operations and alerting supervisors upon noticing any equipment abnormality, process anomaly, or safety hazard.

Regulatory & Quality Compliance Framework

Candidates must demonstrate operational awareness and rigorous adherence to the following regulatory chapters and international standards governing this role:

WHO Good Manufacturing Practices

Main Principles for Pharmaceuticals
Fundamental quality assurance, production sanitation, and quality control requirements for pharmaceutical products.

Schedule M (Revised)

Indian cGMP Statutory Guidelines
Legal guidelines governing building layouts, cleanroom airlocks, HVAC validation, and personnel hygiene.

ICH Q10 Quality System

Modern Pharmaceutical Quality
Comprehensive model across process development, commercial manufacturing, and continual quality improvement.

ALCOA+ Data Integrity Standards

Good Documentation Governance
Principles ensuring all physical and digital records remain Attributable, Legible, Contemporaneous, Original, and Accurate.

Tailored Resume Guidelines for Clinical Data & Database Roles

  • Highlight targeted skill keywords relevant to Clinical Data & Database Roles prominently in your technical skills block.
  • Ensure project details and laboratory/clinical instrumentation (e.g. HPLC, Argus, EDC, Veeva) are explicitly listed.
  • Keep the resume layout clean, modern, and formatted for high-ranking automated ATS parsing.

Technical Interview Assessment & Guidance

Q: What core technical competencies make you suitable for Clinical Data & Database Roles at Medpace?
Authoritative Answer: Discuss your hands-on experience, academic foundation, understanding of standard workflows, and compliance awareness.
Q: How do you ensure data integrity and documentation precision in your daily workflow?
Authoritative Answer: Reference ALCOA+ principles, SOP adherence, real-time documentation practices, and prompt deviation reporting.
Q: Why do you want to join Medpace in this role?
Authoritative Answer: Highlight Medpace’s market reputation, quality culture, and your commitment to contributing to their operational goals.

Mandatory Documents Checklist for Interview & Verification

Ensure you organize the following original credentials and self-attested photocopies for technical interviews and HR onboarding verification:

Curriculum Vitae (2 Hard Copies)
Updated, clean chronological CV featuring core instrumentation, software tools, and role-relevant achievements.
Academic Certificates & Marksheets
Original and self-attested copies of 10th, 12th, Graduation, and Post-Graduation marksheets and degree certificates.
Government Photo Identification
Original Aadhaar Card and PAN Card (mandatory for statutory PF/ESI registration) plus Passport or Driving License.
Past 3 Months Salary Slips & Bank Records
Official payslips and corresponding bank statement records validating salary credits (for experienced candidates).
Relieving & Appointment Letters
Appointment letter and latest increment letter from current firm, plus relieving letters from all prior employers.
Passport Photographs & Professional Registration
4 recent passport-size color photographs, plus State Pharmacy Council registration certificate (where applicable).

Frequently Asked Questions (FAQ)

Q: What is the official application deadline for Clinical Data & Database Roles at Medpace?
Answer: Applications are processed on a rolling basis. Candidates are encouraged to apply as early as possible while the opening is active.
Q: Are freshers eligible for this specific role?
Answer: Freshers (0 years experience) are welcome if indicated in the experience tag; otherwise relevant domain background is required.
Q: Does Pharma Speed Post charge any recruitment fee?
Answer: No. Pharma Speed Post provides 100% free career notifications with zero charges.

Related Career Pathways & Functional Specializations

Associated functional specializations and recruitment tracks for Clinical Data & Database Roles at Medpace:

Medpace Recruitment 2026Medpace Careers IndiaMedpace Clinical Data & Database Roles VacancyClinical Data & Database Roles Jobs in Unit 1203, 12th Floor, Building Q2, Aurum QPark, TTC Industrial Area, Thane Belapur Road, Navi Mumbai (Maharashtra) – 400710Clinical Data Management CareersMedidata Rave EDC SpecialistClinical Data Coordinator OpeningseCRF Design and Discrepancy ManagementCDM Freshers Vacancies IndiaB Pharmacy Jobs 2026M Pharmacy Pharmacology CareersMSc Chemistry Jobs Pharma IndustryBSc Life Sciences CareersPharma Jobs in Unit 1203, 12th Floor, Building Q2, Aurum QPark, TTC Industrial Area, Thane Belapur Road, Navi Mumbai (Maharashtra) – 400710Pharma Speed Post Verified Careers100% Free Pharma Job Portal

Application Procedure

  1. Carefully review the functional eligibility criteria, academic qualifications, and key duties specified for Clinical Data & Database Roles at Medpace above.
  2. Calibrate your resume to highlight relevant instrumentation, software platforms, or cGMP/GCP regulatory compliance.
  3. Ensure your contact details, active mobile number, and email address are up to date in your CV.
  4. Click the official application button below to access the direct employer recruitment portal or HR email channel with zero intermediary charges.

👉 Submit Official Application – Clinical Data & Database Roles at Medpace

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