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We are seeking a dedicated and enthusiastic Trainee Physician to contribute to our clinical development projects. This role offers an exciting opportunity to gain hands-on experience in a pharmaceutical company focused on developing innovative medicines for patients with underserved medical dermatology diseases.
Tasks and Responsibilities
In collaboration with Clinical Lead, Clinical Study Physician trainee would provide medical input to the following activities
-Clinical Study Protocol Development:
- Collaborate with the Clinical Lead to elaborate on clinical study synopses and protocols.
- Conduct literature reviews to inform study design decisions.
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-Clinical and Medical Content Review:
- Thoroughly review study protocols, amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and other clinical documents.
- Ensure accuracy, consistency, and alignment with regulatory requirements.
-Clinical Trial Oversight:
- Be an integral part of the Clinical Study Team overseeing trial execution by the Contract Research Organization (CRO).
- Provide medical input to address queries from Ethics Committees and Health Authorities.
- Assist sites in determining patient eligibility by addressing medical questions.
- Perform data reviews for ongoing trials, including blinded safety data assessments
- Medical degree
- Enthusiasm and Dedication: We seek someone passionate about clinical research and committed to advancing patient care.
- Attention to Detail: Precise review of clinical documents ensures data accuracy and patient safety.
- Team Player: Collaboration within the Clinical Study Team and with external partners is crucial.
- High English Proficiency: Proficient in both written and spoken English.
- Care
- Innovation
- Courage
- Simplicity