Associate Director/Director, Clinical Science

Job description

Associate Director/Director, Clinical Science

Lycia Therapeutics |

Lycia Therapeutics | Posted Feb 16

Full-time

Unknown

Lycia Therapeutics is a biotechnology company using its proprietary lysosomal targeting chimera (LYTAC) platform to discover and develop best-in-class therapeutics that degrade extracellular and membrane-bound proteins. These proteins drive a wide range of difficult-to-treat diseases, including autoimmune and inflammatory conditions. Lycia was established in 2019 in collaboration with academic founder and Nobel Laureate Carolyn Bertozzi, Ph.D., professor of chemistry and HHMI investigator at Stanford University. In May 2024, Lycia Therapeutics completed a $106.6 million Series C financing to advance its pipeline of LYTAC extracellular protein degraders to the clinic. Lycia is headquartered in South San Francisco.

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Lycia Therapeutics is seeking a Director or Associate Director of Clinical Science who will play a critical role in the design, execution, and analysis of clinical trials of clinical stage assets. This position is responsible for driving clinical development activities, ensuring scientific integrity, and collaborating with cross-functional teams to advance innovative therapies through all stages of clinical development. At Lycia, you will be instrumental in shaping the development trajectory of our innovative therapeutic candidates and bringing transformative therapies to patients in need.

Key Responsibilities

Provides clinical and scientific contributions to the clinical development plans, including the designing and implementation of clinical studies

Contribute to the development of clinical strategies in alignment with program goals

Clinical Development Leadership

Responsible for development of study protocols, case report forms (CRFs), consent forms, investigators brochure, development of charters (e.g., Independent Data Monitoring Committee, Safety Monitoring Committee) and other essential trial documents

Contributes to the development of training modules, Investigator webinars, Investigator meetings, and

CRA/staff training

Ensure compliance with ICH-GCP guidelines, regulatory requirements, and internal policies

Act as a medical monitor or scientific liaison during studies, depending on qualifications, to partner with investigators, study site staff, and CRO partners,

Data Analysis and Reporting

Analyze clinical data to evaluate safety, efficacy, and pharmacological properties of investigational products

Uses available tools to monitor study conduct (screening, randomization, adjudication, retention)

Participates in and leads safety and data cleaning activities (medical listing review, periodic safety review, preparation for IDMC review)

Provide input on the quality control of tables, listings, and graphs for database lock

Collaborate with biostatisticians to interpret results and prepare clinical study reports for regulatory submissions

Cross-Functional Collaboration

Work closely with clinical operations, regulatory affairs, biostatistics, and other cross-functional teams to ensure seamless trial execution

Build relationships and engage with external stakeholders such as Key Opinion Leaders (KOLs), investigators, and regulatory authorities as needed to help advance the development of investigational products

Regulatory Submissions

Support the preparation of regulatory documents (e.g., INDs, DSURs, NDAs) by providing clinical expertise

Ensure that all clinical trial data meet regulatory standards for safety and efficacy

Team Management and Mentorship

Depending on candidate’s experience level, opportunity to actively mentors and coaches junior cross-functional team members

Minimum Requirements

Education

Director: MD/PhD or MD or equivalent advanced degree in life sciences or related field

Associate Director: Advanced degree (PhD, PharmD, RN, Master’s) in life sciences; MD preferred but not required

Experience

Minimum 5–8 years (Director) or 3–5 years (Associate Director) of experience in clinical research or drug development within biotech/pharma settings

Expertise in allergy, immunology or autoimmune therapeutic areas is highly desirable

Skills

Strong understanding of drug development processes from preclinical to Phase 2 clinical development is desirable

Proficiency in analyzing and interpreting complex clinical data

Excellent communication skills for cross-functional collaboration and external stakeholder engagement

Competencies And Capabilities

Advanced knowledge of clinical trial design methodologies, biostatistics, and regulatory requirements

Ability to anticipate risks and develop mitigation strategies during trial execution

Demonstrated ability to lead cross-functional teams in a fast-paced environment while managing multiple priorities

Flexible and dynamic interpersonal approach, entrepreneurial by nature, a collaborative team player who works well with physicians, scientists, managers, peers, and staff

Creates an environment for open scientific debate, integrates information, and drives to decisions or actions where no process/precedent exists

Location & Travel

San Francisco Bay Area preferred; Ability to work on-site (Lycia South San Francisco office) at least 2-3 full days per week

Business travel as needed (may vary with time, but is not expected to exceed 15%)

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

The expected base salary range for this role is $190,000-$225,000 for Associate Director and $237,000-$280,000 for the Director. We encourage candidates of all levels to apply as there is often flexibility on job title and responsibilities. Compensation will be based on a variety of factors, including experience, qualifications and internal equity. Lycia offers a competitive employment package that includes an annual bonus, equity, and a generous benefits package.

About the company

Lycia Therapeutics

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Worksite address

south san francisco, CA, 94083, US

Who can apply

Review the original listing for work authorization, qualifications and employer requirements.