Medical Monitor Ontario, Canada

ClinChoice Inc.; Maryland; Hybrid; USD 90,000 - 130,000; Full time

Job summary

ClinChoice Inc. is searching for a qualified Medical Monitor to join our team. This hybrid role encompasses advising on clinical trials and data analysis while providing oversight from study design to dissemination of results. The successful candidate will possess a medical degree and relevant clinical experience, contributing to high-quality patient care and safety in the healthcare industry.

Qualifications

• At least two years of medical experience.
• Previous knowledge of the clinical trial process.
• Fluent in English.

Responsibilities

• Provide clinical support throughout the clinical trial lifecycle.
• Answer medical questions and provide advice during project meetings.
• Review clinical study data and write protocols and reports.

Skills

Medical knowledge

Analytical skills

Communication skills

Microsoft Office proficiency

Education

University Degree in medical disciplines

Job description

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a Medical Monitor on a permanent basis. This is a hybrid position, to be based either in Quebec, Canada or Pennsylvania, US.

The Medical Monitor will provide clinical support to the Clinical Operations team from study design through to dissemination of the results.

Join our team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career!

Main Job Tasks and Responsibilities:

• Will be the Clinical Advisor for the entire lifecycle of the clinical trial by answering medical questions.
• Participates in the project meetings by giving medical advice.
• Reviews study data listing from a medical point of view.
• Analyzes and makes an independent interpretation of study data/results.
• Writes and reviews protocol, Case Report Forms (CRF) and Clinical Study Reports (CSR).
• Provides training in specific disease/therapeutic area.
• May provide study team with assistance in developing criteria for investigator site selection and networking for potential investigators for study participation.
• Participates in subject recruitment and retention activities which may include per sponsor request individual calls to Key Opinion Leaders, Investigators and site staff, and participation in teleconference and virtual presentations.
• May present protocol and safety reporting information at Investigator Meetings (as required).
• Provides on-call coverage for medical queries on the protocol.

Education, Experience and Skills

• University Degree in medical disciplines.
• At least two (2) years of medical experience
• Previous experience or knowledge of the clinical trial process.
• Fluent in English and local language(s).
• Proficiency in Microsoft Office (e.g. Word, Excel, Outlook).
• Willingness to travel.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

Who will you be working for?

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. We are on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Join our passionate team and make a meaningful impact on global healthcare!

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology.The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice Canada Inc. is proud to be an equal opportunity employer, valuing and respecting diversity. We are committed to inclusive, barrier-free recruitment and selection processes. We will accommodate the needs of qualified applicants under theHuman Rights Code and theAccessibility for Ontarians Disabilities Act, in all aspects of the hiring process, upon request by calling + 1 [phone] x 301.

We thank all applicants for their interest; however, only those being considered for an interview will be contacted. In accordance with Federal Personal Information Protection and Electronic Documents Act ("PIPEDA"),personal information is collected under the authority of theActand will only be used for candidate selection.

Key words: Medical Monitor, Clinical Research Physician, Medical Doctor, MD, CRO, Contract Research Organisation

#LI-LG1 #LI-Senior #LI-FULLTIME

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