Medical Scientist (Medical Degree Required)
- Buenos Aires
- Permanente
- Tiempo completo
We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.
Our Clinical Development model centers on the customer and the patient.
We continually seek ways to simplify and streamline our work to make Syneos Health easier to work with and for.
Whether joining 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 therapy delivery because we are passionate about changing 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 growth, supportive management, training, peer recognition, and rewards.
We foster a Total Self culture where you can be authentic.
We are dedicated to caring for our people.
We value diversity of thoughts, backgrounds, and perspectives to create a sense of belonging.
Job Responsibilities Serving as a clinical team member for data review, including verification of subject eligibility based on medical history.
Applying 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), drafting and responding to site queries, and ensuring accurate safety data reconciliation.
Reviewing reactogenicity data in eDiaries or EDC systems for protocol compliance.
Assisting lead clinicians with data review, safety narratives, and presentation slide preparation.
Supporting additional tasks like literature reviews, data cleaning, and review of training materials.
Participating in safety surveillance meetings and contributing to PowerPoint presentations as needed.
Being available during normal business hours for the assigned region.
Additional responsibilities may include study startup or conduct activities such as eDiary design, feasibility, informed consent reviews, protocol reviews, safety presentations, and site interactions for safety follow-up or protocol compliance.
Note: No interaction with regulatory authorities or direct site contact in this role.
Qualifications Medical degree.
At least 2 years of direct patient care experience post-residency.
Experience reviewing safety data, SAEs, and patient criteria as a medical monitor.
Experience with InForm or RedCap.
Experience working on vaccine trials.
Ability to critically evaluate medical/scientific information.
Understanding of clinical program and study design, development, and execution.
Ability to adapt to a fast-paced, changing environment.
No pharmaceutical industry experience required.
Preferred: training in infectious diseases or infection control, experience with investigational trials and systems (e.g., INFORM, J-review), and proficiency with MS Office tools.
Get to know Syneos Health Over the past 5 years, we've worked with 94% of FDA-approved drugs, 95% of EMA products, and conducted over 200 studies across 73,000 sites and 675,000+ patients.
Join us to challenge the status quo and make a difference in a dynamic environment.
Learn more at Additional Information Tasks and responsibilities may be expanded at the company's discretion.
Qualifications may be considered equivalent based on experience or education.
This description does not constitute a contract.
We are committed to compliance with applicable laws and promoting an inclusive, accessible workplace.
Work here matters everywhere.
Our work helps deliver therapies to those in need, and a career with us guarantees a meaningful impact on patients' lives worldwide.
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