Medical Monitor Associate – Dermatology & Rheumatology CRO
Location: India (Remote)
Job Type: Permanent, Full-Time
Experience Required: Minimum 1 year in CRO, pharmaceutical industry, or clinical trials
Job Category: Clinical Research / Medical Affairs / Pharmacovigilance
Company Overview
Indero (formerly Innovaderm) is a global clinical research organization specializing in dermatology and rheumatology trials. With over 25 years of experience, Indero provides end-to-end clinical trial solutions, including protocol design, patient recruitment, monitoring, biometrics, and study execution. Operating across North America, Europe, Asia Pacific, and Latin America, Indero partners with biotech and pharmaceutical sponsors to ensure scientific rigor, operational excellence, and efficient trial delivery.
Role Overview
Reporting to the Team Lead, Medical Monitoring, the Medical Monitor Associate provides medical, scientific, and administrative support across study-level, department-level, and cross-functional activities. This role focuses on clinical oversight in dermatology and rheumatology trials, ensuring protocol compliance, accurate data review, and high-quality documentation. The position is ideal for board-certified dermatologists with clinical research experience.
Key Responsibilities
Maintain up-to-date knowledge of study protocols, amendments, Investigator’s Brochure, safety updates, and relevant clinical research guidelines.
Support development and implementation of Medical Monitoring plans.
Enter medical queries in EDC after lead monitor review and support adverse event, medical history, and concomitant medication coding.
Conduct photo reviews, assess efficacy scores, and support clinical data validation.
Assist in drafting SOPs and working practices related to Medical Monitoring activities.
Prepare and maintain study trackers, KPI trackers, and relevant documentation, ensuring timely filing and e-signature completion.
Coordinate project-level medical indication training and team trainings.
Support business development through proposal preparation and presentations.
Participate in team meetings and cross-functional coordination with CRO, PM, DM, and statistical teams.
Perform additional responsibilities as assigned by the Director, Scientific and Regulatory Affairs.
Qualifications & Requirements
Medical degree; board-certified dermatologist.
Minimum 1 year of experience in CRO, pharmaceutical industry, or clinical trials. Experience as a medical monitor, medical reviewer, or drug safety physician is an asset.
Strong knowledge of drug development, clinical trial protocols, GCP, and applicable FDA and Health Canada regulations.
Ability to work independently and collaboratively in a matrix environment.
Excellent organizational, multitasking, and prioritization skills.
Strong verbal, written, and interpersonal communication skills.
Proficiency in Microsoft Word, Excel, and PowerPoint.
Work Environment & Benefits
Remote-first position with occasional meetings outside standard business hours.
Flexible work schedule and full-time employment.
Ongoing learning, professional development, and career advancement opportunities.
Collaborative, innovative, and high-performance culture.
Equal Opportunity
Indero is committed to equitable treatment and providing accommodations for applicants with disabilities. Applicants must have legal authorization to work in India.
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