ClinChoice is seeking a Medical Monitor to join their team. The Medical Monitor will provide clinical support to the Clinical Operations team throughout the entire lifecycle of clinical trials, from study design to the dissemination of results. This is a hybrid position based in either Quebec, Canada, or Pennsylvania, US.Responsibilities:
Acting as the Clinical Advisor by answering medical questions.
Participating in project meetings and providing medical advice.
Reviewing study data listings from a medical perspective.
Analyzing and independently interpreting study data and results.
Writing and reviewing protocols, Case Report Forms (CRF), and Clinical Study Reports (CSR).
Providing training in specific disease/therapeutic areas.
Assisting in developing criteria for investigator site selection and networking.
Participating in subject recruitment and retention activities.
Presenting protocol and safety reporting information at Investigator Meetings.
Providing on-call coverage for medical queries related to the protocol.
Requirements:
University Degree in medical disciplines.
At least two (2) years of medical experience.
Previous experience or knowledge of the clinical trial process.
Fluency in English and local language(s).
Proficiency in Microsoft Office (e.g., Word, Excel, Outlook).
Willingness to travel.
ClinChoice offers:
Opportunity to make a difference in peoples’ lives.
ClinChoice is a global provider of regulatory and scientific services, specializing in preparing and submitting compliant Material Safety Data Sheets (MSDS/SDS). The company supports multinational chemical manufacturing companies, offering hazard analysis, SDS authoring, and regulatory compliance expertise across US, EU, and other international markets. ClinChoice focuses on establishing structured processes for SDS preparation, and delivers comprehensive hazard assessments and SDS phrases based on global regulatory standards. They provide mentorship and review services.