Associate Medical Director

ARTO; Greater London; On-site; GBP 80,000 - 120,000; Full time

Job summary

An established industry player is seeking an Associate Medical Director to join their growing clinical development team. This exciting opportunity involves supporting drug development up to the IND/BLA submission phase within a globally renowned pharmaceutical company. The role requires strong expertise in clinical development, regulatory support, and data analysis, ensuring compliance and quality throughout the process. If you are passionate about advancing treatments in the Rare Disease space and have a strong background in the pharmaceutical industry, this position offers a chance to make a significant impact in a collaborative environment.

Qualifications

• 2+ years of pharmaceutical industry experience required.
• Experience in Rare Disease is preferred.

Responsibilities

• Develop key trial documents and support regulatory submissions.
• Analyze clinical trial data and ensure data quality.
• Act as scientific lead liaising with various stakeholders.

Skills

Clinical Development

Regulatory Support

Data Analysis

Stakeholder Communication

Risk Mitigation

Education

MD or MD/PhD

Job description

Helping biotech and pharma companies place Medical Director-Vice President level candidates in clinical development in the fields of Immunology

ARTO is currently partnered with a globally renowned mid-sized pharmaceutical company committed to developing drugs within the Rare Disease space.

With a growing clinical development team, they are seeking an Associate Medical Director to assist with drug development up to the IND/BLA submission phase.

Key Responsibilities:

1. Document Development & Regulatory Support: Create key trial documents (e.g., IND Annual Reports, Investigator Brochures, Briefing Books) and support regulatory submissions in compliance with guidelines.
2. Clinical Development & Study Design: Contribute to Clinical Development Plans (CDPs), develop protocols and methodologies, and collaborate on Statistical Analysis Plans (SAPs) ensuring alignment with project timelines.
3. Scientific & Safety Data Oversight: Analyze and interpret clinical trial data, perform safety reviews, ensure data quality, and support safety reporting (e.g., DSURs, SUSARs).
4. Communication & Collaboration: Act as the scientific lead liaising with stakeholders (e.g., PIs, KOLs, DMCs, Pharmacovigilance, Biometrics), ensuring effective study execution and GCP compliance.
5. Governance & Risk Mitigation: Represent Clinical Science in study teams, manage study-specific plans, deliver timely results, and proactively identify risks and mitigation strategies for successful trials.

Experience Needed:

• MD or MD/PhD
• At least 2 years of experience in the pharmaceutical industry
• Rare Disease experience preferred

If interested, please apply through the job advertisement or contact me at [e-mail].

Additional Details

• Seniority level: Director
• Employment type: Full-time
• Job function: Science and Research
• Industries: Staffing and Recruiting

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