Medical Scientist , and ARG - MD

Medical Scientist (UK, CAN, and ARG only - MD required)

Updated: Yesterday
Location: G
-Remote
Job :

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do.

• Must be located in Canada, UK, or Argentina to be considered.
• MD (Medical Degree) required.
• Minimum 2 years of direct patient care experience post-residency required.
• Previous Medical Monitoring experience required.
• Serving as a clinical team member assigned to data review for clinicians, including verification of subject eligibility based on medical history.
• Critical application of protocol-defined study requirements to assess data relevant to study endpoints (e.g., safety, tolerability, immunogenicity, efficacy).
• Reviewing serious and non-serious adverse events (AEs), including drafting and responding to site queries and ensuring accurate and timely reconciliation of safety data.
• Reviewing reactogenicity data in eDiaries or EDC systems to ensure compliance with protocol-specified safety surveillance and monitoring.
• Assisting the lead clinician with aggregate data review and interpretation, preparation and management of safety narratives, slide development for internal and external presentations, oversight or participation in safety narrative authoring workflows.
• Supporting additional study-related tasks such as literature reviews, data cleaning, review of training materials, participating in safety surveillance meetings and contributing to PowerPoint creation as needed.
• Being available during normal business hours for the assigned region and working the specified number of hours per week.
• Additional responsibilities may be added based on prior experience, including study startup or conduct activities such as eDiary design, feasibility, informed consent document reviews, draft protocol reviews, safety presentations, and site interactions for safety follow up or protocol compliance and/or training.
• Note:
  
  There is no interaction with regulatory authorities or direct contact with site staff in this role.

• Medical degree (M.D).
• Previous experience as a Medical Monitor.
• Ability to critically evaluate medical/scientific information.
• Understanding of the design, development, and execution of clinical programs and studies.
• Capacity to adapt to a fast pace and changing environment.
• No pharmaceutical industry experience required.
• Training and experience in infectious diseases and/or infection control in the hospital setting preferred.
• Experience with investigational clinical trials preferred.
• Experience with investigational clinical trials systems (e.g., INFORM, REDCAP, J-review) preferred.
• Experience with Excel, Word documents, PowerPoint preferred.

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description.

At Syneos Health, we are dedicated to building a diverse, inclusive, and authentic workplace. If your past experience doesn’t align perfectly, we encourage you to apply anyway. At times, we take into consideration transferable skills from previous roles. We also encourage you to join our Talent Network to stay connected to additional career opportunities.

Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against. If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, including the use of this website, please contact us at:
Email:  One of our staff members will work with you to provide alternate means to submit your application.

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