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Job Descrption

The successful candidate will be an essential part of the Biology team focusing on the design, implementation, and oversight of in vivo Pharmacology studies.  The candidate will contribute to multiple cross-functional teams focused on developing new Attobody therapeutics for patients with autoimmune and inflammatory diseases.  Projects requiring Pharmacology support may span from target validation, preclinical development, to translational biology.  This position requires previous experience managing in vivo Pharmacology studies in an industry setting, with experience in immunologic models strongly preferred.  Job responsibilities also include assessing and coordinating with CRO’s.  This is an on-site position.

Key Responsibilities

• Oversee the design, implementation, and conduct of in vivo Pharmacology studies.
• Identifying, assess, and work with various contract research organizations (CRO’S) to generate critical pharmacokinetic, pharmacodynamic, and efficacy data.
• Work collaboratively on multiple projects concurrently.  Includes developing and presenting Pharmacology plans and data at project team meetings and to management to support project objectives. 
• Support the filing of regulatory documents, including writing study reports and IND (or related) documents.

Basic Qualifications

• MS/PhD in Immunology/Biology/Oncology or other relevant discipline.
• At least 8-10 years of experience designing, executing, and overseeing in vivo Pharmacology studies to support projects in the pharmaceutical or biotech industry.
• Critical thinking, multitasking, and the ability to propose new approaches and ideas.
• Excellent troubleshooting, data analysis and interpretation skills are required.
• Capable of working independently in a fast-paced, team-oriented environment, demonstrating the ability to manage activities on multiple projects simultaneously.
• Great communication skills and team spirit are a must.

Preferred Qualifications

• Management experience is strongly preferred.
• Successful history of coordinating off-site in vivo work via CRO’s is strongly preferred.
• Experience in translational biology.  Work with ex vivo models desired.
• Previous project team leadership in the pharmaceutical or biotech industry.

About Attovia 
Attovia is creating a pipeline of biotherapeutics with initial focus immune-mediated disease. The company leverages Attobody™, a novel biologics platform, to generate small format biparatopic binders that expand the addressable target universe across disease areas and can offer stronger efficacy, faster speed to response, and an improved safety profile than traditional approaches. We are currently progressing multiple programs across immune mediated disease indications. Our culture is centered around five core pillars:  • Integrity  • Learning & Growth  • Drive for Excellence  • Innovation  • Teamwork & Collaboration 
We take pride in fostering a strong team and dynamic work environment, and we are seeking individuals who align with our values and contribute to a positive and impactful workplace.    Attovia is located in Fremont, CA, with planned future relocation to the mid-Peninsula area.  Attovia is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.  
Learn more about Attovia: www.attovia.com 

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