Senior Director, Clinical Operations

BigHat; San Mateo (CA); On-site; USD 275,000 - 295,000; Full time

Benefits offered by this job

Health insurance

401(k) with company match

Paid parental leave

DTO, shutdown days, holidays

Job summary

BigHat in San Mateo, CA is hiring a Senior Director, Clinical Operations to lead the clinical operations function in early-stage biologics development for oncology and inflammatory diseases. The role blends strategic oversight and hands-on execution, aligning trials with regulatory expectations and company goals.

You will guide trial design, site selection, biomarker integration, data quality, and documentation while building a high-performing team in a fast-paced startup environment.

Qualifications

• Advanced degree in life sciences, pharmacy, or related field.
• 10+ years in clinical operations, with oncology/inflammatory disease focus.
• Experience leading early-phase trials in biotech/pharma.
• Proven ability to build and lead startup-style teams.
• In-depth knowledge of ICH-GCP, FDA/EMA regulations, and global processes.
• Vendor management, CRO oversight, budget and risk management experience.
• Site-side sample management and biomarker program support experience.
• Data management and data quality oversight familiarity.
• Experience generating clinical documents across trial lifecycle.
• Exceptional communication, leadership, problem-solving skills.
• Experience in oncology, inflammatory diseases, and/or targeted therapies.

Responsibilities

• Develop and execute clinical operational strategies to advance biologics from early phase to regulatory approval.
• Lead planning, initiation, and management of Phase I–III trials with regulatory compliance.
• Oversee CROs, labs, and vendor management; monitor site monitoring activities.
• Manage site sample collection, processing, storage, and shipment per protocol.
• Partner with Translational Biomarker teams to support biomarker sampling plans.
• Oversee data management, quality reviews, and audit-ready datasets.
• Prepare and manage key clinical documents and regulatory submissions.

Skills

Leadership

Clinical Operations

Vendor management

CRO oversight

Budget management

Trial risk management

Biomarkers

Data management

ICH-GCP

Regulatory knowledge

Education

Advanced degree in life sciences or related field

Job description

Senior Director, Clinical Operations

Department: Drug Development

Employment Type: Full Time

Location: San Mateo, CA

Description

The role: We are seeking an experienced and motivated Clinical Operations Lead to join our drug development team, focusing on early-stage clinical development of biologic drugs in oncology and inflammatory diseases. As the Director and Lead of Clinical Operations, you will oversee the design, execution, and management of clinical trials, ensuring alignment with corporate objectives and regulatory requirements. You will lead a high-performing clinical operations function, develop strategies to accelerate development timelines, and establish best practices for trial execution. This is a unique opportunity to contribute at both strategic and operational levels in a fast-paced, collaborative startup environment.

Key Responsibilities

Leadership & Strategy

• Develop and execute clinical operational strategies to advance biologics for oncology and inflammatory diseases from early-phase trials to regulatory approval.
• Collaborate with cross-functional teams (e.g., R&D, Regulatory, CMC, Translational Biomarkers) to align clinical strategies with overall company goals.
• Provide insights into trial design, site selection, and patient recruitment strategies.
• Serve as a key point of contact for internal and external stakeholders, including investigators, regulators, and partners; prepare for and support regulatory interactions and inspections.

Clinical Trial Execution

• Lead the planning, initiation, and management of clinical trials (Phase I–III), ensuring they are conducted on time, within budget, and in compliance with global regulatory standards (ICH-GCP, FDA, EMA) and company SOPs.
• Oversee vendor selection and management, including CROs, labs, and other external partners; conduct and manage CRO site monitoring activities to ensure protocol adherence and data integrity.
• Monitor trial progress, manage risks, and resolve operational challenges efficiently.
• Oversee clinical site‑side sample management, including collection, processing, storage, and shipment of biological samples in alignment with protocol requirements and chain‑of‑custody standards.

Translational Biomarker Support

• Partner closely with the Translational Biomarker team to ensure clinical operations infrastructure supports biomarker sample collection, handling, and logistics across all trial sites.
• Coordinate with sites and CROs to ensure biomarker sampling plans are implemented correctly and that sample quality and completeness meet program requirements.

Data Management and Quality

• Oversee clinical data management activities, including data completeness, quality review, and timely query resolution to ensure high‑quality, audit‑ready datasets.
• Implement and maintain data quality management processes in collaboration with data management and biostatistics partners.

Clinical Document Generation

• Manage the preparation and lifecycle of key clinical documents, including protocols, informed consent forms, investigator brochures, clinical study reports, and regulatory submissions, ensuring accuracy, timeliness, and compliance with applicable guidelines.
• Coordinate cross‑functional input and review cycles to deliver complete, high‑quality documentation.

Budget and Resource Management

• Develop and manage clinical operations budgets, ensuring cost‑effective resource allocation.
• Optimize timelines and resources to meet critical milestones and deliverables.

Skills Knowledge and Expertise

• Advanced degree in life sciences, pharmacy, or a related field (PhD, MD, PharmD preferred).
• 10+ years of experience in clinical operations, with a strong track record in oncology and/or inflammatory diseases.
• Experience leading operational aspects of early‑phase clinical trials in the biotech or pharmaceutical industry.
• Demonstrated ability to build and lead teams in a dynamic, startup environment.
• In‑depth knowledge of ICH‑GCP guidelines, FDA/EMA regulations, and global clinical trial processes.
• Proven experience in vendor management, CRO oversight, budget management, and trial risk management.
• Experience in clinical site‑side sample management and biomarker program support.
• Familiarity with data management principles and data quality oversight in clinical trials.
• Experience managing the generation of clinical documents across the trial lifecycle.
• Exceptional communication, leadership, and problem‑solving skills.
• Experience in oncology, inflammatory diseases, and/or molecularly targeted therapies.

Total Rewards

The salary estimated for this position is $275,000 - $295,000 + bonus + options + benefits. Compensation will vary depending on job‑related knowledge, skills, and experience. Actual compensation will be confirmed in writing at the time of the offer.

What BigHat Offers:

• Range of health insurance plan options through Anthem and Kaiser (monthly credit if benefit waived)
• Dental, and vision coverage through Guardian
• Additional well‑being benefits through Nayya, OneMedical, Wagmo, Rula, and more
• 401(k) with company match
• DTO, two weeks of company‑wide shutdown, and 12 company holidays
• Paid parental leave