Remote Medical Director, Safety & Risk Leadership

Alphanumeric; Philippines; Remote; PHP 11,307,000 - 15,075,000; Full time

Job summary

Alphanumeric is seeking a SERM Medical Director (Remote, 1-Year Contract) to lead safety evaluation, risk management, and regulatory interactions for a global pharmaceutical program. The role requires MD qualification and strong pharmacovigilance expertise, with English communication in a fast-paced, matrixed environment.

Working remotely from the Philippines, you will align safety activities across clinical development and marketed products, supporting RFIs and regulatory submissions while

Qualifications

• MD or equivalent physician qualification.
• Experience in clinical development, drug safety or pharmacovigilance.
• Experience responding to Health Authority RFIs.
• Strong benefit-risk assessment and safety evaluation understanding.
• Experience supporting regulatory submissions and authorities interactions.
• Excellent scientific writing and English communication.

Responsibilities

• Lead safety evaluation and benefit-risk assessments.
• Support pharmacovigilance and risk management activities.
• Contribute to regulatory submissions and health authority interactions.
• Prepare and review responses to RFIs.
• Analyze clinical and safety data for regulatory decisions.
• Participate in cross-functional safety governance.
• Provide protocol and regulatory support across development lifecycle.
• Escalate significant safety concerns when appropriate.

Skills

Independent work

Scientific writing

English proficiency

Regulatory interactions

Education

MD or equivalent physician qualification

Job description

Alphanumeric is seeking a SERM Medical Director (Remote, 1-Year Contract) to lead safety evaluation, risk management, and regulatory interactions for a global pharmaceutical program. The role requires MD qualification and strong pharmacovigilance expertise, with English communication in a fast-paced, matrixed environment.

Working remotely from the Philippines, you will align safety activities across clinical development and marketed products, supporting RFIs and regulatory submissions while