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

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. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

Job Responsibilities

*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.

• 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 Participant in safety narrative authoring workflows. -Supporting additional study-related tasks as required, such as:

• Literature reviews.

• Data cleaning.

• Review of training materials.

• -Participating in safety surveillance meetings and contributing to PowerPoint creation asneeded.

• -Being available during normal business hours for the assigned region and working the specified number of hours per week.

• -A dditional 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.

Qualifications

• · Medical degree (M.D)

-Previous experience as a Medical Monitor

• Possesses the ability to critically evaluate medical/scientific information.

• Understands 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 is preferred.

• Experience with investigational clinical trials is preferred.

• Experience with investigational clinical trials systems ( i.e INFORM, REDCAP, J-review) is preferred.

• Experience with excel, word document, PowerPoint is preferred.