Vice President, Clinical Pharmacology

4 weeks ago

Watertown, United States Acrivon Therapeutics Full time

Our global team operates out of two leading life science clusters, Watertown, MA and Medicon Village in Lund, Sweden.

**Position Overview**:
**Duties and Responsibilities**:

- Closely participate in the design, implementation, and interpretation of pharmacological studies, ensuring robust methodology and compliance with regulatory standards.
- Lead pharmacokinetic and pharmacology analyses at the clinical development stage.
- Support the clinical dose strategy and selection process through analysis of preclinical and early clinical studies.
- Collaborate with cross-functional teams, including research and development, clinical development, regulatory affairs, and program management, to define and implement successful development strategies.
- Serve as a key scientific spokesperson for the company, comfortable presenting pharmacology data with authority at internal meetings, medical/scientific conferences, and with corporate partners.
- Ensure scientific excellence and integrity in all pharmacological data published or communicated to regulatory bodies.

**Qualifications include**:

- Pharm D and/or PhD in Clinical Pharmacology or Biochemistry.
- At least 10 years of experience in oncology clinical pharmacology, with a significant track record in clinical drug development in an industry setting.
- Solid understanding of clinical objectives, constraints and risks in drug safety and efficacy
- Proven leadership experience with the ability to successfully manage cross functional relations.
- Strong knowledge of the drug development process, particularly in oncology, including IND/NDA enabling studies.
- Excellent strategic thinking and problem-solving skills.
- Demonstrated ability to work effectively in a collaborative, fast-paced team environment.
- Strong communication and interpersonal skills, proficient in presenting scientific data and strategies to stakeholders including non-scientific audiences.

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