As a Safety Admin, you'll focus on serious and non-serious adverse events, protocol inquiries, physician assessment of diagnostics, Data and Safety Monitoring Boards, and Endpoint Adjudication Committees
Job Summary
As a Safety Admin, you'll focus on serious and non-serious adverse events, protocol inquiries, physician assessment of diagnostics, Data and Safety Monitoring Boards, and Endpoint Adjudication Committees.
You will liaise and establish effective relationships with internal functional team members to implement projects, prepare contractual documents, coordinate and facilitate meetings, and accurately manage all incoming safety documentation.
The role requires maintaining pharmacovigilance audit readiness and supporting global and domestic programs across multiple clinical trials.
Matching Summary
As a Safety Admin, you'll focus on serious and non-serious adverse events, protocol inquiries, physician assessment of diagnostics, Data and Safety Monitoring Boards, and Endpoint Adjudication Committees.
Skills & Requirements
Must-have
Adverse event coordination
Data Safety Monitoring Board liaison
Contractual document preparation
Project meeting facilitation
Pharmacovigilance audit readiness
Data entry and tracking systems
Strong problem solving skills
Nice-to-have
Ability to work independently
Effective communication skills
Positive and professional demeanor
Flexibility to reprioritize workload
Training junior staff
Key Requirements
High / Secondary school diploma or equivalent
Relevant formal academic or vocational qualification
At least 2 years of comparable experience
Knowledge of FDA Regulations and ICH Good Clinical Practices