Senior Clinical Research Director, I&I

Scorpion Therapeutics; United States; Remote; USD 150,000 - 250,000; Full time

Job summary

A leading global healthcare company seeks a Senior Clinical Research Director to lead clinical programs. This role involves mentoring teams, providing medical expertise, and supporting regulatory submissions. Join a dynamic environment that fosters growth and offers a comprehensive rewards package.

Benefits

Comprehensive rewards package

Health and wellbeing benefits

Generous parental leave

Qualifications

• Fluency in English (spoken and written).
• At least 4 years of experience in the pharmaceutical industry or CRO.
• Background in clinical development.

Responsibilities

• Mentor other CRDs and Clinical Scientists on projects.
• Provide leadership and coordinate action plans to resolve study issues.
• Offer medical expertise for clinical studies and registries.

Skills

Leadership

Analytical skills

Emotional intelligence

Self-motivation

Education

Medical Doctor (MD)

Job description

About The Job

We are an innovative global healthcare company dedicated to advancing science to improve lives. We offer a dynamic environment where you can grow your career, make connections, and explore new opportunities. Ready to join us?

The Senior Clinical Research Director (Sr CRD)

The Sr CRD serves as the primary clinical lead for programs, requiring a well-organized, strategic, and resourceful individual with excellent emotional intelligence, self-motivation, and analytical skills to manage multiple operational tasks.

Responsibilities of the Senior CRD

1. Mentor other CRDs and Clinical Scientists on projects and collaborate to ensure aligned operational approaches.
2. Provide leadership, build consensus, and coordinate action plans to resolve study issues, sharing lessons learned across teams.
3. Escalate study or project issues to TA Heads and share relevant information within and beyond project teams.
4. Offer medical expertise for clinical studies and registries, including protocol review and key results analysis.
5. Support clinical development activities such as feasibility assessments, data review, and risk assessments.
6. Contribute to submission dossiers for regulatory agencies, including FDA, EMA, Japan, and China.
7. Provide medical input and support for study activities, training, data review, and medical information dissemination.
8. Prepare documents and presentations for internal governance meetings.
9. Assist in defining product value propositions, target product profiles, and market access strategies in collaboration with relevant teams.
10. Represent the project at regulatory agency meetings as the medical spokesperson.
11. Lead the development of clinical sections for regulatory submissions and support registration activities.
12. Perform additional roles as needed, including reviewing clinical documentation and evaluating licensing candidates.

Minimum Qualifications

Medical Doctor (MD) preferred, with fluency in English (spoken and written). At least 4 years of experience in the pharmaceutical industry or CRO, with a background in clinical development.

Why Join Us?

• Contribute to life-changing scientific advancements with a supportive team.
• Enjoy opportunities for growth and career development, both locally and internationally.
• Benefit from a comprehensive rewards package recognizing your contributions.
• Access health and wellbeing benefits, including high-quality healthcare and generous parental leave.

We are committed to diversity and equal opportunity. All qualified applicants will be considered without regard to race, gender, or other protected characteristics.