Director, Clinical Development

Position Title: Director, Clinical Development

Reports to: Vice President, Clinical Development

Status: Fulltime, Exempt

Location: South San Francisco, CA (Hybrid)

Summary:

This is an opportunity to work in a dynamic role, supporting the development of clinical study strategy and managing the subsequent protocol development, execution, interaction with regulatory agencies and ethics committees, medical monitoring, interpretation and presentation of clinical trials associated with the clinical development of novel and innovative drugs for viral diseases and other indications. This role requires an MD and serves as a lead medical monitor for company-sponsored studies.

Specific responsibilities include, but are not limited to :

Designing and executing clinical development plans and protocols for clinical trials in viral diseases and other indications. This includes collaborating with the functional team during program implementation, clinical study start-up/execution/close out, data analysis/reporting and support of NDA/MAA/ROW filings

Serving as the medical monitor for company-sponsored clinical trials, providing real-time medical oversight to investigators and sites, including eligibility determinations, dose modification and toxicity management, and responses to protocol-related medical queries

Developing and maintaining study-level Medical Monitoring Plans and medical data review plans; overseeing CRO medical monitors and ensuring consistent application of protocol and medical monitoring guidelines across sites

Performing ongoing medical review of safety and laboratory data, including target-organ safety signals (e.g., hepatic signals such as ALT elevations, hepatitis flares, and drug-induced liver injury assessment), and partner with Drug Safety/Pharmacovigilance on SAE and SUSAR assessment, causality, and benefit-risk evaluation

Participating in the Safety Review Team and serving as the clinical interface to independent Data Monitoring Committees; contributing to the safety surveillance plan and to study-level risk management and stopping/pausing criteria

Providing high level, complex scientific and clinical guidance to Clinical Trials Management, Biometrics, Regulatory and Project Management to meet project deliverables and timelines

Serving as a clinical point of contact for senior management and senior level teams, both internally and externally

Providing medical and clinical input to key study documents and data tools, including informed consent forms, case report forms, statistical analysis plans, and data edit checks

Authorship of key clinical documents, including protocols, clinical study reports, and regulatory filings

Managing the clinical research component in the preparation/review of regulatory documents, IND annual reports/DSURs, IND safety reports, Investigator Brochures, and development plans; supporting responses to health authority and ethics committee/IRB questions and support inspection readiness for medical monitoring activities

Coordinating the collection and assimilation of ongoing data for internal analysis and review, and coordinating the preparation and/or review of data listings, summary tables, study results and scientific presentations

Presenting scientific and clinical study information at investigator meetings, internal meetings, and external meetings, and engage key opinion leaders and external experts in virology, infectious diseases, and other relevant therapeutic areas

Mentoring and providing medical guidance to clinical science and clinical operations staff, as applicable

Participating in the evaluation of business development opportunities

This job description outlines the primary duties and responsibilities of the role; however, it is not intended to be all-inclusive. The scope of responsibilities may be modified, expanded, or adjusted at the discretion of the organization to meet evolving business needs.

Qualifications include:

MD (or DO, or an equivalent non-US medical degree) is required

Minimum of 5 years of experience in clinical development in the biotechnology, pharmaceutical, or CRO setting, or equivalent academic clinical research experience, including hands-on experience as a medical monitor or in safety review of clinical trials

Preferred: board certification or eligibility in Infectious Diseases, Gastroenterology/Hepatology, or Internal Medicine; direct experience in virology / infectious disease will be considered uniquely qualified

Clinical trial experience either in the academic setting (as an investigator or sub-investigator) or in industry (as a director or medical monitor) with hands-on patient care and clinical practice experience

Thorough understanding of GCP and familiarity with relevant FDA and ICH guidance, including adverse event management and safety reporting requirements

Working knowledge of statistics as applied to clinical trial design and analysis

Ability to think analytically and strategically to formulate, develop, and execute clinical plans

Experienced with engaging internal and external expert physicians, scientists, and other key stakeholders in constructive scientific and clinical dialog around study design, study conduct, and interpretation of clinical results

Experience working with CROs and other external resources, including oversight of CRO medical monitors

Preferred: experience interacting with regulatory agencies (e.g., FDA, EMA) on clinical development programs

Demonstrated ability to work in a team environment. Able to thrive in a small group setting that requires a high energy, hands-on attitude. Must be capable of working with attention to detail in a time sensitive environment.

Experience in writing and editing scientific research reports

The ability to absorb new information quickly and gain command of relevant literature along with the skills to analyze and concisely summarize complex data and information

Pay Range: $289,000 - $312,600 annualized

The stated pay range for this position reflects the San Francisco Bay Area job market. Assembly Bio establishes pay ranges based on geographic work locations. Additional factors such as academic credentials and relevant experience will influence the actual salary offered .

About Assembly Bio

Assembly Bio (NASDAQ: ASMB) is an ambitious biopharmaceutical company with cutting-edge therapeutic candidates capable of improving the lives of millions living with devastating viral and liver diseases. We have multiple ongoing clinical programs focused on the development of novel treatments for herpesviruses, hepatitis delta virus (HDV), cholestatic liver diseases and hepatitis B virus (HBV). Further, our research organization is dedicated to the discovery of new therapies to change the treatment paradigm for individuals living with serious viral and liver diseases.

We pride ourselves on creating a culture and work environment that is scientifically driven, ambitious, and collaborative. We encourage diversity of thought that leads to great innovation and are looking to add great people to our dynamic team who are driven to transform the lives of patients. We set our sights high—and pursue our goals with determination. Our unique organization stands ready to welcome talented, motivated individuals, who share our ambitions.

As an equal opportunity employer, we are committed to diversity and inclusion and will

not tolerate discrimination and harassment of any kind. All employment decisions are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental s