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Any Advanced PG Diploma Programs Just 19999/-

ENROLL HERE - (only from India)

 Any Advanced PG Diploma Programs

Now just 19999/- only

Duration: 6 Months

Only from India please pay from here

ADVANCED PG DIPLOMA IN
CLINICAL RESEARCH & PHARMACOVIGILANCE

The Advanced PG Diploma in Clinical Research & Pharmacovigilance from PharmaExa – the world’s largest and most respected clinical research and CRO institution – equips you with mastery of clinical trial design, regulatory compliance, and Good Clinical Practice, alongside specialist skills in drug safety, adverse event reporting, and risk management. Rooted in ICH-GCP and WHO standards, this globally recognised certification prepares you to excel in CROs, pharmaceutical companies, and regulatory agencies, leading advancements in clinical excellence and public health protection.

ADVANCED PG DIPLOMA IN
CLINICAL RESEARCH & CLINICAL DATA MANAGEMENT

The Advanced PG Diploma in Clinical Research & Clinical Data Management from PharmaExa – the world’s largest and most trusted clinical research and CRO institution – equips you with in-depth expertise in clinical trial processes, regulatory compliance, and Good Clinical Practice, alongside the skills to manage and analyse clinical data to global standards. Grounded in ICH-GCP and CDISC guidelines, this globally recognised certification prepares you to lead ethically, work to the highest standards, and make a meaningful impact in the advancement of healthcare worldwide.

ADVANCED PG DIPLOMA IN
PHARMACOVIGILANE & CLINICAL DATA MANAGEMENT

The Advanced PG Diploma in Pharmacovigilance & Clinical Data Management from PharmaExa – the world’s largest and most trusted clinical research and CRO institution – provides comprehensive training in drug safety, adverse event reporting, and risk management, combined with the expertise to organise, manage, and analyse clinical data to international benchmarks. Rooted in global regulatory standards and CDISC compliance, this globally recognised certification empowers you to safeguard public health, ensure ethical excellence, and excel in the evolving landscape of clinical research.

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International accreditations & Recognizations

Programme Overviews – Career Impact & Credentials

At PharmaExa – the world’s largest and most globally recognised clinical research and CRO institution – our flagship Advanced Postgraduate Diplomas are designed to shape future leaders in the life sciences industry. Whether you choose Clinical Research & Pharmacovigilance, Clinical Research & Clinical Data Management, or Pharmacovigilance & Clinical Data Management, each programme is meticulously structured to meet international industry standards and employer expectations worldwide.

Career Impact
These qualifications open doors to high-impact roles across Contract Research Organisations (CROs), pharmaceutical companies, biotechnology firms, clinical trial units, and regulatory authorities. Graduates are equipped not only with technical expertise but also with the ethical integrity and global perspective demanded in safeguarding public health, leading research teams, and managing large-scale clinical projects.

Course Duration & Format
Each diploma is completed over 6 months through a flexible learning format that blends interactive online lectures, cutting-edge eBooks, real-world case studies, and curated interview questions with model answers for career preparation. This approach enables both professionals and graduates to balance their studies with existing commitments while gaining practical, industry-relevant experience.

Certification, Accreditation & Global Recognition
On completion, participants earn a globally recognised certification accredited by leading international bodies in clinical research and pharmacovigilance education. Recognised across continents, these credentials hold strong value in the UK, EU, USA, Middle East, and Asia, enabling graduates to compete for prestigious positions in the global life sciences job market.

Core Specialisations

  • Advanced PG Diploma in Clinical Research & Pharmacovigilance – Comprehensive training in clinical trial design, protocol development, site management, and monitoring procedures in accordance with ICH-GCP and WHO guidelines. In addition, students master pharmacovigilance systems, adverse event detection and reporting, signal detection methodologies, and post-marketing drug safety surveillance.

  • Advanced PG Diploma in Clinical Research & Clinical Data Management – Strong focus on end-to-end clinical trial operations, ethical and regulatory compliance, Good Clinical Practice, and quality assurance. Learners gain in-depth skills in electronic data capture (EDC) systems, CRF design, data validation, query management, and database lock procedures, ensuring accuracy and integrity of trial data.

  • Advanced PG Diploma in Pharmacovigilance & Clinical Data Management – Specialised training in drug safety regulations, benefit–risk assessment, expedited reporting, and global pharmacovigilance legislation. The data management modules cover database programming, integration of safety data with clinical trial databases, and compliance with regulatory submission standards such as CDISC and FDA 21 CFR Part 11.

By choosing PharmaExa, you invest in a qualification that commands respect, opens global career opportunities, and equips you to lead in clinical research, data management, and drug safety on an international stage.

Course level : Advanced
Duration : 6 Months
Examination Type : Module wise
Eligibility : Graduation in the Life Science (B.Sc/ M.Sc.), Pharmacy(B.Pharm/ M.Pharm), Nursing (B.Sc./M.Sc) Medical science courses (MBBS, BDS etc.)
Admission process : Evaluation Basis
Average salary : INR 4,50,000- INR 7,00,000 per year (Terms and Conditions applied)
Recruiting Organizations : Contract Research Organizations, 2. Information Technology Companies, Hospitals etc
Job Positions

Graduates of these programmes can pursue diverse roles such as Clinical Research Associate (CRA), Clinical Trial Coordinator, Regulatory Affairs Associate, Medical Writer, Quality Assurance Auditor, Project Manager, Drug Safety Associate, Pharmacovigilance Scientist, Signal Detection Specialist, Case Processing Specialist, Safety Database Coordinator, Clinical Data Manager, Data Validation Associate, CDM Programmer, and Data Quality Analyst—positions that are in high demand across CROs, pharmaceutical companies, biotech firms, regulatory bodies, and healthcare organisations worldwide.