Global Safety Senior Medical Director - Oncology

SciPro; United States; Remote; USD 120,000 - 180,000; Full time

Job summary

Join a forward-thinking biotech company as a Global Safety Senior Medical Director specializing in Oncology. This remote position offers a competitive salary and significant career growth opportunities. You will lead safety analyses for clinical trials, manage risk mitigation strategies, and serve as a Safety Subject Matter Expert. The role is ideal for those with a solution-oriented mindset and a passion for oncology, providing a chance to make a meaningful impact in a stable and innovative environment. Apply now to embark on this exciting journey!

Qualifications

• 7+ years of experience in pharmacovigilance and safety in biotech or pharma.
• Proven experience in oncology is essential for this role.

Responsibilities

• Conduct safety analyses for clinical trials and post-marketed products.
• Lead clinical safety aggregate reports and manage risk mitigation strategies.
• Communicate safety updates to stakeholders and oversee safety surveillance.

Skills

Pharmacovigilance

Oncology Expertise

Risk Management Plans (RMPs)

Clinical Safety Reporting

Signal Management

Education

Medical Director Qualification

Job description

Global Safety Senior Medical Director - Oncology

Position Overview: We are seeking a highly experienced Global Safety Senior Medical Director specializing in Oncology to join our team remotely. This role offers a competitive compensation package based on experience and provides significant career growth opportunities within a rapidly expanding biotech company.

Company Profile:

SciPro Global partners exclusively with a stable and fast-growing company that is advancing a diverse pipeline across Therapeutic Areas including Oncology, Cardiovascular, Immunology, CNS, and Respiratory. Currently, over 30 programs are in Phase 1 & 2, fueling substantial growth in their Safety group. The team is solution-oriented, collaborative, and led by a passionate leader in the US, reporting directly to the Oncology Therapeutic Area Safety Head.

Key Responsibilities:

1. Conduct safety analyses for clinical trials and post-marketed products.
2. Lead clinical safety aggregate reports such as PADERs.
3. Manage risk mitigation and minimization strategies, including working with RMPs.
4. Respond to health authority queries related to safety and risk in regulatory documents.
5. Perform signal management and lead signal strategy measures.
6. Oversee safety surveillance of assigned products.
7. Serve as Safety SME, liaising with clinical counterparts across the organization.
8. Communicate safety updates to internal and external stakeholders.
9. Provide safety input during clinical study design activities.
10. Identify and implement improvements within the safety team and group.

Minimum Requirements:

1. Medical Director or equivalent qualification.
2. At least 7 years of pharmacovigilance and safety experience within biotech or pharma sectors.
3. Proven oncology experience is required.
4. Solution-oriented mindset and motivated attitude.

Additional Details:

This position is ideal for professionals seeking to grow their career in a reputable company with a stable and innovative environment. Apply now to start your journey with us!