CTM-CDM-PV Training Specialist
Budget: ₹37,500 – ₹75,000 INR
We run a training program in Clinical Research and management and are looking to strengthen it with a rigorous, practice-oriented teaching module. We seek an experienced industry professional who can guide graduate students through the end-to-end lifecycle of clinical trials, with integrated coverage of:
Clinical Trial Management (CTM)
Clinical Data Management (CDM)
Pharmacovigilance (PV)
Essentials of Medical Writing
Role & Responsibilities
You will be responsible for both curriculum design and delivery, with a strong focus on real-world application.
Specifically, you will:
Design a cohesive, integrated syllabus that logically connects CTM, CDM, PV, and Medical Writing across the clinical trial lifecycle
Deliver live lectures and workshops (online and/or on-site) using real-world case studies and practical examples
Develop and share slide decks, curated reading materials, and short assessments to track student progress
Review and provide structured feedback on student work, including:
Mock study protocols
Data cleaning and query management exercises
Safety case narratives and reports
Clinical or regulatory writing samples (e.g., CSR sections, summaries)
Your teaching should prepare students to meet industry-ready standards, not just theoretical knowledge.
Acceptance Criteria
A detailed course outline submitted prior to the first session
Teaching materials shared at least 48 hours before each class
End-of-course evaluation demonstrating that ≥80% of students meet defined learning objectives
Preferred Expertise
Strong working knowledge of ICH-GCP guidelines
Familiarity with MedDRA, CDISC standards (SDTM/ADaM)
Exposure to common EDC platforms or drug safety systems
Prior experience teaching, mentoring, or training graduate-level learners is a strong plus
Ideal Candidate Profile
If you:
Enjoy mentoring early-career professionals
Can translate complex regulations into clear, actionable guidance
Prefer hands-on, application-driven teaching over purely theoretical instruction
we would welcome the opportunity to collaborate.
Engagement Details
Mode: Freelance / Visiting Faculty
Delivery: Online and/or On-site (Hyderabad)
Schedule: Flexible (weekday or weekend sessions)
Clinical Trial Management (CTM)
Clinical Data Management (CDM)
Pharmacovigilance (PV)
Essentials of Medical Writing
Role & Responsibilities
You will be responsible for both curriculum design and delivery, with a strong focus on real-world application.
Specifically, you will:
Design a cohesive, integrated syllabus that logically connects CTM, CDM, PV, and Medical Writing across the clinical trial lifecycle
Deliver live lectures and workshops (online and/or on-site) using real-world case studies and practical examples
Develop and share slide decks, curated reading materials, and short assessments to track student progress
Review and provide structured feedback on student work, including:
Mock study protocols
Data cleaning and query management exercises
Safety case narratives and reports
Clinical or regulatory writing samples (e.g., CSR sections, summaries)
Your teaching should prepare students to meet industry-ready standards, not just theoretical knowledge.
Acceptance Criteria
A detailed course outline submitted prior to the first session
Teaching materials shared at least 48 hours before each class
End-of-course evaluation demonstrating that ≥80% of students meet defined learning objectives
Preferred Expertise
Strong working knowledge of ICH-GCP guidelines
Familiarity with MedDRA, CDISC standards (SDTM/ADaM)
Exposure to common EDC platforms or drug safety systems
Prior experience teaching, mentoring, or training graduate-level learners is a strong plus
Ideal Candidate Profile
If you:
Enjoy mentoring early-career professionals
Can translate complex regulations into clear, actionable guidance
Prefer hands-on, application-driven teaching over purely theoretical instruction
we would welcome the opportunity to collaborate.
Engagement Details
Mode: Freelance / Visiting Faculty
Delivery: Online and/or On-site (Hyderabad)
Schedule: Flexible (weekday or weekend sessions)