Senior Clinical Trial Manager

Regulatory Toolkit; San Francisco (CA); On-site; USD 180,000 - 220,000; Full time

Job summary

Marea Therapeutics, a South San Francisco biotechnology company, seeks a Senior Clinical Trial Manager to lead day-to-day clinical trial execution for MAR001 and MAR002 programs. You will manage CROs and vendors, mentor staff, and drive study start-up, enrollment, and close-out while ensuring GCP/regulatory compliance.

The role is onsite at least three days/week in South San Francisco, with compensation aligned to experience and program scope.

Qualifications

• BA/BS or higher in a relevant scientific discipline.
• 6–9 years of clinical research/clinical operations in pharmaceutical/biotech.
• Global Ph 2–3 trial experience required.
• Experience leading cross-functional study execution teams.
• Experience with vendor management, negotiating contracts and RFPs.
• Strong attention to detail with high-quality outputs (presentations, reports, dashboards).
• Able to work in fast-paced environment across multiple time zones.
• Excellent written and oral communication skills.
• High level of professionalism with internal and external stakeholders.
• In‑depth knowledge of current regulatory requirements and guidelines (ICH‑GCP).

Responsibilities

• Lead the day-to-day execution and management of clinical trials, ensuring studies are conducted efficiently, on time, within budget, and in compliance with GCP and regulatory requirements.
• Oversee CROs and vendors to ensure high‑quality delivery and milestones across programs.
• Mentor junior team members as needed within the Clinical Operations team.
• Support start-up, enrollment, maintenance, and close‑out activities for MAR001/MAR002 studies.
• Contribute to study design input and regulatory submissions support.
• Manage study budgets and operating plans, ensuring adherence to budgets.
• Support inspection readiness and SOP development within Clinical Operations.

Skills

Clinical Operations

Vendor Management

Cross-functional Team Leadership

ICH-GCP Knowledge

Regulatory Submissions

Communication Skills

Problem Solving

Project Management

Education

BA/BS in science

Job description

ABOUT THE COMPANY

Marea Therapeutics is a clinical‑stage biotechnology company based in South San Francisco with a growing pipeline of first‑in‑class therapies to address genetically validated cardioendocrine disease targets. Our therapies have the potential to serve as transformative treatment options for significant patient populations living with cardioendocrine diseases.

The company’s lead program, MAR001, is being developed for the treatment of severe hypertriglyceridemia (sHTG), a condition characterized by very high triglyceride levels and elevated risk of acute pancreatitis. Preclinical models with MAR001 demonstrated reduction in triglycerides, remnant cholesterol and ectopic fat, and improved insulin sensitivity. MAR001 has demonstrated strong and a differentiated profile in patients and is approaching Phase 3 development. Our second clinical asset, MAR002, is a monoclonal antibody targeting excess growth hormone produced by the pituitary gland in the rare hormonal disorder, acromegaly. MAR002 has potential to become best‑in‑disease and is quickly progressing into Phase 2/3 clinical development. We also have a third asset that is swiftly advancing through research discovery, with DC nomination expected this year.

At Marea, we believe in the power of collaboration and the importance of leading by example. We are a tight‑knit team that values the contributions of every member, from interns to senior leaders. Our environment is dynamic, with each day presenting new challenges and opportunities for growth. Every role is “Hands‑On”,and the successful candidate will be able to work alongside team members, regardless of level, to understand challenges and drive results.

ABOUT THE ROLE

Reporting to the Sr. Director of Clinical Operations, the Senior Clinical Trial Manager (Sr. CTM) will lead the day‑to‑day execution and management of clinical trials, ensuring studies are conducted efficiently, on time, within budget, and in compliance with GCP and regulatory requirements.

This role is a hands‑on operational leader at the study level, responsible for driving execution across study start‑up, enrollment, maintenance, and close‑out activities. The Sr. CTM will work closely with Senior Clinical Operations Leaders as well as with cross‑functional partners and oversee CROs and vendors to ensure high‑quality delivery of clinical trial milestones. There may be the opportunity to mentor junior members of the Marea team.

In this role, Sr. CTM will be a key clinical operating team member supporting our MAR001 program, specifically help drive the execution of a global PH2B study. MAR001 is a potential first‑in‑class‑and monoclonal antibody indicated for severe hypertriglyceridemia (sHTG),

This is a full‑time, South San Francisco based position with the expectation of working onsite at least three days per week. The level of the role will be commensurate with the chosen applicant’s background and experience.

KEY RESPONSIBILITIES

Study Execution Leadership & Management

• Support program lead with setting and timely executing the development strategies for the clinical studies.
• Responsible for the strategic and operational oversight, management, execution, and delivery of the clinical studies for MAR002 and related clinical program activities.
• Lead the Study Management Team (SMT) for assigned clinical study.
• Resolve and/or escalation issues raised by the clinical operations team or the SMT.
• Ensure consistency between studies for assigned clinical program.

CRO and Vendor Management

• Support vendor selection, including request for proposals, leading bid defense meetings, critical review of contracts and negotiation of work orders.
• Oversee CROs and other selected vendors on a product level including setting and monitoring key performance indicators and ensuring successful execution of the clinical program/studies and may co‑lead operational governance meetings.

Study Planning, Risk Mitigation, and Enrollment

• Identification and oversight of potential challenges or risks with clinical study conduct and implementation of mitigation plans.
• Support the development and execution of clinical site engagement and subject recruitment strategies for assigned study.

Trial Design, Documentation, and Submissions Support

• Provide input and clinical operations perspective on clinical trial design.
• Author, provide input and/or oversee the development of key study level documents as well as provide support for regulatory submissions.

Study Budget Management & Operational Excellence

• Oversee financial aspects of assigned clinical study, including preparing related operating plans and ensuring adherence to planned study budgets.
• Support Clinical Operations department head with strategic initiatives and the implementation of those initiatives for process and operational improvements.

Inspection Readiness, Quality, and SOP Support

• Oversee/co‑lead inspection readiness activities as it relates to clinical study execution and act as subject matter expert during regulatory inspections.
• Support Clinical Operations department on clinical SOP development.
• Support Clinical Operations department on ad hoc initiatives to leverage best practices as well as new technologies and applications for clinical study conduct.

QUALIFICATIONS

• BA/BS or higher degree in a relevant scientific discipline required.
• Significant experience (6 - 9 years) of clinical research / clinical operations and organizational management within the pharmaceutical industry; Biotech/small pharma experience preferred.
• Global Ph 2 – 3 clinical trial experience required
• Experience leading and working on cross functional study execution teams.
• Demonstrated ability to present complex information to management, vendors and external audiences.
• Demonstrated ability to manage and communicate effectively with vendors including negotiating contracts, drafting and reviewing request for proposals, analyzing scope of work, responding to inquiries and complaints.
• Strong attention to detail and ability to generate high quality work outputs (e.g. presentations, reports, dashboards, etc.)
• Demonstrated ability to work in a fast‑paced environment with multiple competing tasks and demands, across multiple time zones.
• Demonstrated ability to work independently, take initiative, complete tasks to deadlines and support Clinical Operations team in doing the same.
• Excellent written and oral communication skills.
• High level of professionalism with internal and external stakeholders.
• Demonstrated problem‑solving skills and conflict management skills.
• In‑depth knowledge of current regulatory requirements and guidelines governing clinical research (e.g., ICH‑GCP).

PAY RANGE

In compliance with applicable pay transparency laws, the expected base salary range for this position is $180,000 - $220,000 annually. This range represents the Company's good faith estimate of the salary range for this role at the date of hire and is subject to change.

WORKING CONDITIONS

• Prolonged periods of being at a stationary desk or work computer
• Ability to occasionally adjust, handle, or move objects up to [20] pounds
• Transparently and timely communicating with others to exchange information
• Occasional travel as required to meet business objectives

We do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual’s status in any group or class protected by applicable federal, state, and local law. We invite applications from minorities, women, the disabled, protected veterans, and all other qualified applicants.