Medical Monitor Contractor

About the role

The Medical Monitor Contractor will serve as a critical member of the clinical team, responsible for ensuring the integrity and quality of clinical data and supporting clinical oversight activities.

Responsibilities

• Serve as a clinical team member assigned to data review for clinicians, including verification of subject eligibility based on medical history.
• Apply protocol‑defined study requirements to assess data relevant to study endpoints (e.g., safety, tolerability, immunogenicity, efficacy).
• Review serious and non‑serious adverse events (AEs), draft and respond to site queries, and ensure accurate and timely reconciliation of safety data.
• Review reactogenicity data in eDiaries or EDC systems to ensure compliance with protocol‑specified safety surveillance and monitoring.
• Assist the lead clinician with aggregate data review and interpretation, preparation and management of safety narratives, slide development for internal and external presentations, and oversight or participation in safety narrative authoring workflows.
• Support additional study‑related tasks such as literature reviews, data cleaning, review of training materials, participation in safety surveillance meetings, and PowerPoint creation as needed.
• Be available during normal business hours for the assigned region and work the specified number of hours per week.
• Additional responsibilities may include 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.

Qualifications

• Medical degree (MD, DO, MBBS, or equivalent) required.
• At least 2 years of direct patient care experience post‑residency (preferred).
• Comfortable with complex medical reviews involving pediatric, adult, and obstetrical populations.
• Prior experience as a medical monitor, including safety data review (non‑serious and serious AEs).
• Experience on an interventional clinical trial within the past 3 years (vaccine trials preferred but not required).
• Familiarity with EDC platforms (RedCap preferred).
• Strong ability to critically evaluate medical/scientific information.
• Understanding of clinical study design, development, and execution.
• Proficiency in Microsoft Word, PowerPoint, and Excel.
• Fluency in English (written and spoken).
• Ability to adapt to a fast‑paced and evolving environment.
• Training and experience in infectious diseases and/or infection control in a hospital setting (preferred).
• Relevant specialty experience such as Family Medicine, Internal Medicine, Obstetrics and Gynecology, or Pediatrics.

Pay

Payrate: $86.85 – $86.85 per hour.

Non‑exempt positions are eligible for overtime at 1.5 × the base hourly rate for hours worked in excess of 40 in a work week, or as required by state or local law. Final offer amounts are determined by factors including relevant skills, education, and experience.

Benefits

• Medical, dental, and vision insurance.
• Health savings accounts with qualified medical plan enrollment.
• 10 paid days off.
• 3 days paid bereavement leave.
• 401(k) plan participation with employer match.
• Life and disability insurance.
• Commuter benefits.
• Dependent care flexible spending account.
• Accident insurance.
• Critical illness insurance.
• Hospital indemnity insurance.
• Accommodations and reimbursement for work travel.
• Discretionary performance or recognition bonus.
• Sick leave and mobile phone reimbursement (as required by state or local law).