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 globally recognized clinical research organization specializing in dermatology and rheumatology trials. With over 25 years of experience, Indero provides end-to-end clinical trial solutions—from protocol design, patient recruitment, and monitoring to biometrics and study delivery. 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 study execution.
Role Overview
The Medical Monitor Associate will report to the Team Lead, Medical Monitoring and Medical Affairs. This role provides medical, scientific, and administrative support for clinical trials, focusing on dermatology and rheumatology studies. The associate will assist in study-level, department-level, and cross-functional activities, ensuring clinical oversight, protocol compliance, and high-quality data management. This position is ideal for board-certified dermatologists with experience in clinical research or medical monitoring.
Key Responsibilities
Maintain current knowledge of study protocols, amendments, Investigator’s Brochure, safety information, and relevant clinical research guidelines.
Support development and implementation of Medical Monitoring plans.
Enter medical queries in EDC following lead medical monitor review.
Conduct coding review of adverse events, medical history, and concomitant medications to ensure proper classification.
Perform photo review and efficacy data assessment for assigned studies.
Support business development activities, including proposal development and client presentations.
Assist in drafting and updating standard operating procedures and working practices related to Medical Monitoring.
Maintain study trackers, KPI trackers, and medical monitoring documentation.
Coordinate team meetings, trainings, and project-level medical indication training sessions.
Ensure timely filing of eSignature documents and maintenance of study documentation.
Provide cross-functional support as needed, including collaborating with project teams, sponsors, and investigators.
Qualifications
Medical degree; board-certified dermatologist.
Minimum 1 year of experience in a CRO, pharmaceutical industry, or clinical trials as a medical monitor, medical reviewer, or drug safety physician.
Strong knowledge of drug development processes, clinical trial protocols, and regulatory guidelines (FDA, Health Canada, and ICH-GCP).
Ability to work independently and collaboratively in a matrixed team environment.
Excellent verbal and written communication skills.
Proficiency in Microsoft Word, Excel, and PowerPoint.
Detail-oriented with strong organizational and multitasking abilities.
Work Environment & Benefits
Remote-first position with some meetings outside standard business hours.
Flexible work schedule and full-time employment.
Opportunities for ongoing learning, professional development, and career advancement.
Collaborative, innovative, and responsive work culture.
Equal Opportunity
Indero is committed to equitable treatment and equal opportunity for all individuals. Reasonable accommodations are provided for applicants with disabilities upon request. Applicants must have legal authorization to work in India.
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