ClinChoice is a full-service global clinical CRO dedicated to offering high-quality, efficient and flexible solutions to pharmaceutical, biotechnology, medical device, and consumer products clients worldwide. With a 25-year history of success, ClinChoice continues to be The Standard of Excellence for biostatistics, clinical operations, data management, statistical programming, CDISC, regulatory affairs, medical affairs and pharmacovigilance. ClinChoice has established major delivery centers across US, China, Europe, Canada, India, Japan and the Philippines. It has over 4,000 employees globally, with a strong and talented team, and a growing clinical operations presence in seven countries across Asia, North America and Europe.
The Medical Monitor (MEM) plays a crucial role in providing clinical support to Clinical Operations throughout the entire lifecycle of a clinical trial, from study design to the dissemination of results. The responsibilities and job requirements for this role are outlined below:
Responsibilities:

Clinical Advisory Role:

Acts as a clinical advisor for the entire lifecycle of the clinical trial, addressing medical questions.
participates in project meetings, providing medical advice.

Data Analysis and Interpretation:

Reviews study data listings from a medical perspective.
Analyzes and independently interprets study data/results.

Document Writing and Review:

Writes and/or reviews protocols, Case Report Forms (CRF), and Clinical Study Reports (CSR).

Training and Support:

Provides training in specific disease/therapeutic areas.
Assists the study team in developing criteria for investigator site selection.
Networks for potential investigators for study participation.

Subject Recruitment and Retention:

Participates in subject recruitment and retention activities.
May make individual calls to key opinion leaders, investigators, and site staff per sponsor request.
Presents protocol and/or safety reporting information at investigator meetings as requested by the sponsor.

On-Call Coverage:

Provides on-call coverage for medical queries related to the protocol.

Job Requirements:

Education:

University Degree in medical disciplines.

Experience:

Minimum of two (2) years of medical experience.

Technical Skills:

Proficiency in Microsoft Office (e.g., Word, Excel, Outlook).

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Medical Monitor Consultant

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