Associate Director/Director, Clinical Science

We are seeking an Associate Director/Director of Clinical Science who will be responsible for providing clinical leadership in the definition of clinical development strategies, as well as the design, execution, and analysis of clinical studies conducted with Surrozen's academic, community and industry partners. This individual should be passionate about working in an innovative therapeutic field. The Associate Director/Director of Clinical Sciences will report to the Senior Director, Clinical Development.

Responsibilities

• Responsible for the review of data listings, summary tables, and study results for multiple clinical trials/programs
• Review and present data for scientific presentations on clinical trial results for internal and external purposes, manuscripts, and regulatory interactions in collaboration with the clinical development team
• Assist in the preparation/review of regulatory documents, clinical protocols, IND annual reports, IND safety reports, Investigator Brochures and BLAs.
• May serve as the primary or supporting medical monitor on clinical trials with appropriate medical backup
• Participate in formulating the clinical development strategy including designing and implementing clinical trials and registrational plans in collaboration with the clinical development team
• Play a key role in management of site/investigator relationships including site initiation visits, investigator calls, and investigator meetings
• Generate company presentations regarding clinical development activities for internal and external stakeholders (i.e. core development teams, executive team, key opinion leaders)
• Work with multiple functional teams to accomplish goals (i.e. clinical development, operations, nonclinical, biostats, research and development, regulatory, CMC, and finance)

• PhD in Biosciences/Clinical Research/Pharmacology or a related subject
• Minimum 3-5+ years of relevant scientific or drug development experience in industry; translational or early clinical trials experience is a plus
• Ability to critically analyze and interpret scientific and clinical data and literature
• Working knowledge of biostatistics, regulatory, clinical pharmacology and pharmacokinetics
• Ability to manage multiple tasks and prioritization skills in a fast-paced environment, work in a collaborative matrixed team environment
• Excellent interpersonal and communication skills (written and verbal)
• Proficient in Microsoft office (Excel, PowerPoint)

Who We Are

Surrozen is a biotechnology company focused on discovering and developing novel regenerative medicines with a focus on unlocking the powerful self-renewal properties of the body through specific control of the Wnt signaling pathway.

Our vision is to engage the body's own biological tissue repair mechanisms with our targeted regenerative antibodies, overcoming research and development hurdles that have been previously intractable, and have held back drug development efforts in the promising area of Wnt biology

We are an Equal Opportunity Employer offering a competitive salary and benefits package.