CIDP - Centre International de Développement Pharmaceutique
Website:
cidp-cro.com
Job details:
Company Description CIDP – Centre International de Développement Pharmaceutique (CIDP) is a private, independent Contract Research Organisation (CRO) established in 2004, specializing in high-performance R&D for the pharmaceutical, cosmetic, and nutrition sectors. With over 17 years of clinical research experience, CIDP operates centers in Brazil, India, Mauritius, and Romania, providing a global platform for research projects. Its services span Research & Development, preclinical in vitro testing, clinical research, biostatistics and data management, and regulatory affairs, all supported by ISO 9001 certified subsidiaries and a dedicated Global Quality Assurance department. CIDP’s multidisciplinary team includes doctors, pharmacists, biostatisticians, biologists, chemists, data managers, and other specialists, backed by an international network of expert investigators. Through its R&I cluster in Mauritius, CIDP leverages unique regional biodiversity to develop innovative natural ingredients and ethno-pharmacology-based solutions for cosmetic, nutrition, and therapeutic applications.
Job Description – Consultant Dermatologist / Principal Investigator
Experience: 1–8 Years
Location: New Delhi
Engagement: Consultant – Flexible Working Hours
Role Overview
CIDP Biotech India Pvt. Ltd. is seeking a Consultant Dermatologist to support dermatology and cosmetic clinical research studies as a Principal Investigator (PI)/Clinical Investigator.
Key Responsibilities
Act as PI for assigned studies and ensure compliance with ICH-GCP, approved protocols, Ethics Committee requirements, and applicable regulations.
Conduct and/or oversee clinical evaluations and dermatological scoring as per study protocols.
Provide medical oversight for participant safety, adverse events, informed consent, and clinical assessments.
Review, provide scientific input, and support finalization of clinical study protocols.
Ensure accurate, complete, and timely clinical documentation and data.
Provide medical/scientific input for Clinical Study Report (CSR) preparation and review.
Collaborate with sponsors, CRO teams, study coordinators, and other stakeholders.
Support monitoring, audits, inspections, and resolution of protocol deviations/clinical queries.
Qualifications
MBBS + MD/DNB Dermatology or equivalent recognized qualification.
1–8 years of relevant experience in Dermatology/Cosmetic Dermatology/Clinical Research.
Experience in clinical scoring, dermatological evaluations, protocol review, or clinical trials preferred.
Good knowledge of ICH-GCP and clinical research practices.
Strong clinical judgment, documentation, and communication skills.
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