Senior Medical Reviewer

Avania; California; Presencial; USD 42.000 - 70.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual bonus

Benefits

Descripción de la vacante

Avania is seeking a Senior Medical Reviewer to lead safety activities for medical device clinical studies. The role involves translating study protocols into practical safety plans and ensuring participant safety concerns are identified and escalated.

Based in Canada, this position oversees multiple studies across therapeutic areas, coordinating with Medical Reviewers and other functions to maintain progress within client budgets and study timelines.

Formación

• Lead safety activities for medical device clinical studies and translate protocols into safety plans.
• Coordinate safety activities across studies with operations and client teams.
• Review clinical information and adverse events; raise questions and escalate safety concerns.
• Facilitate events committees and coordinate adjudication when required.
• Mentor junior medical reviewers as you establish in the role.

Responsabilidades

• Translate study protocols into safety management plans and strategy documents.
• Coordinate safety activities across studies to align with client needs and budgets.
• Review clinical information and adverse events, identify inconsistencies, and escalate concerns.
• Facilitate clinical events committees and coordinate member identification and adjudication.
• Manage competing priorities across studies and therapeutic areas.
• Mentor junior medical reviewers as you gain experience.

Conocimientos

Safety leadership

Clinical study coordination

Adverse event review

Event adjudication

Mentoring

Descripción del empleo

Avania is hiring a Senior Medical Reviewer

Salary Range up to CAD $100,000 + Annual bonus + Benefits

About the Role

As a Senior Medical Reviewer at Avania, you'll lead safety activities for medical device clinical studies, turning protocols into practical safety plans and helping ensure that participant safety concerns are identified, questioned and escalated. This is a clinical operational leadership role, not simply adverse-event processing or data entry.

Based in Canada, you'll typically oversee 5 to 9 studies, depending on their complexity, across areas such as cardiovascular, orthopedics, dermatology and neurology. You'll coordinate the work with Medical Reviewer 1 or 2 colleagues supporting each project. Where a medical monitor is assigned, they provide medical oversight and have the final say on clinical safety decisions.

What You’ll Do

• Translate study protocols and statements of work into safety management plans and other study‑specific strategy documents.
• Coordinate safety activities across your studies, working with clinical operations and other functions to keep work moving and aligned with client needs and study budgets.
• Review clinical information and adverse events, identify inconsistencies or missing information, ask follow-up questions and elevate safety concerns.
• Facilitate clinical events committees where required, including identifying members and coordinating event adjudication.
• Manage competing priorities across studies with different therapeutic areas, complexity and committee requirements.
• As you become established in the role, help mentor junior medical reviewers.