Medical Monitor Associate (Dermatology & Rheumatology) – CRO | India
Company: Indero
Location: India (Home-Based)
Employment Type: Permanent | Full-Time
Industry: Clinical Research | Medical Affairs | Dermatology | Rheumatology
Experience Required: Minimum 1+ year in clinical research within a CRO or pharmaceutical environment
Position Overview
A global dermatology- and rheumatology-focused Contract Research Organization is seeking a Medical Monitor Associate (Dermatologist) to support medical monitoring activities across international clinical trials.
Reporting to the Team Lead, Medical Monitoring within Medical Affairs, this role provides medical, scientific, and operational support at study, departmental, and cross-functional levels. The Medical Monitor Associate plays a key role in ensuring clinical trial safety oversight, data integrity, and protocol compliance while collaborating with project teams, sponsors, and investigative sites.
This position is ideal for board-certified dermatologists with clinical research experience who can balance rigorous protocol requirements with real-world clinical considerations and interpret complex safety and efficacy data efficiently.
Key Responsibilities
Study-Level Medical Oversight
Maintain in-depth knowledge of study protocols, amendments, Investigator’s Brochures, and evolving safety information.
Support development of Medical Monitoring Plans.
Assist in safety data review and enter medical queries in EDC systems following subject-level safety listing review by the Lead Medical Monitor.
Review adverse event coding, medical history, and concomitant medication listings to ensure MedDRA/WHO coding accuracy.
Conduct clinical photo review for dermatology trials.
Review efficacy endpoints and clinical scoring data.
Track KPIs and maintain study trackers.
Coordinate document workflows, including eSignatures and SharePoint filing.
Cross-Functional & Operational Support
Attend project meetings with cross-functional stakeholders including Project Management, Data Management, Biostatistics, and CRO partners.
Develop content for indication-specific medical training at the project level.
Support business development initiatives including proposal development and client presentations.
Assist in drafting and updating SOPs and internal medical monitoring procedures.
Coordinate internal team meetings and training sessions.
Maintain medical monitoring documentation and ensure timely completion.
Required Qualifications
Education:
Medical Degree (MBBS or equivalent).
Board-Certified Dermatologist (mandatory).
Experience:
Minimum 1+ year of experience in clinical research within a CRO or pharmaceutical organization.
Investigator experience in clinical trials may be considered.
Prior experience as Medical Monitor, Medical Reviewer, or Drug Safety Physician is advantageous.
Knowledge & Competencies
Strong understanding of the global drug development lifecycle.
Good knowledge of ICH-GCP guidelines and regulatory frameworks, including familiarity with Health Canada and FDA regulations.
Ability to analyze high-volume clinical and safety data and provide medical recommendations.
Strong collaboration skills within multidisciplinary and matrix teams.
Ability to manage multiple concurrent studies and shifting priorities.
Excellent written and verbal communication skills in English.
Proficiency in Microsoft Word, Excel, and PowerPoint.
Ability to work independently in a remote environment with minimal supervision.
Work Environment & Benefits
This is a home-based full-time position in India.
Flexible work schedule
Permanent employment
Ongoing professional development opportunities
Exposure to global dermatology and rheumatology clinical programs
Note: Occasional attendance at meetings outside regular business hours (primarily evenings) may be required due to global time zones.
About the Organization
Indero is a globally recognized Contract Research Organization specializing in dermatology and rheumatology clinical trials. With over 25 years of expertise, the organization delivers comprehensive clinical development services, including study design, clinical monitoring, medical monitoring, biometrics, pharmacovigilance, and regulatory consulting.
Operating across North America, Europe, Asia Pacific, and Latin America, the organization partners with biotech and pharmaceutical sponsors to deliver scientifically rigorous and operationally efficient global trials.
Equal Opportunity Statement
The organization is committed to equitable employment practices and provides reasonable accommodations during the recruitment process upon request.
Applicants must be legally authorized to work in India.
Apply via ThePharmaDaily.com
If you are a board-certified dermatologist with clinical research experience seeking to advance your career in medical monitoring within a specialized global CRO, apply now through ThePharmaDaily.com and contribute to high-impact dermatology and rheumatology clinical programs worldwide.
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