Senior Clinical Trial Manager

Vera Therapeutics, Inc.; Oregon; Hybrid; USD 150,000 - 180,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401k match

Flexible time off

Paid holidays

Job summary

Vera Therapeutics, Inc. is seeking a Senior Clinical Trial Manager to lead day-to-day global trial operations, ensuring adherence to protocol, SOPs, GCP/ICH, and regulatory requirements.

You will partner with CROs, manage timelines, budgets, and data quality while driving cross-functional collaboration across teams. Ideal candidates have 5+ years in clinical development within pharma/biotech, experience with rare or inflammatory diseases, and a track record of mentoring staff in a fast-paced

Qualifications

• BS or higher in life sciences or health-related field.
• 5+ years clinical development experience in pharma/biotech.
• Experience with rare/inflammatory diseases and difficult enrollments preferred.
• Regulatory filing experience and inspection readiness preferred.
• Experience mentoring junior staff and working in fast-paced environments.
• Proficiency in GCP, ICH guidelines and FDA regulations.

Responsibilities

• Own day-to-day operational oversight of global clinical trials.
• Monitor trial adherence to protocols, SOPs, GCP/ICH standards and KPIs.
• Identify and mitigate risks; manage CRO/vendor relationships.
• Support data quality and issue resolution (eligibility, deviations).
• Develop study plans, ICFs, site manuals, CRF guidelines and system specs.
• Lead clinical operations meetings and cross-functional collaboration.
• Travel up to 30% as needed to support programs.

Skills

Clinical development

GCP/ICH/FDA

Leadership

MS Office

Education

Bachelor's degree in life sciences

Tools

MS Office

Job description

Vera Therapeutics is a commercial-stage biotechnology company focused on the pursuit of truth in science to transform medicine in autoimmune disease, starting with the kidney. Vera Therapeutics' flagship commercial product is TRUTAKNATM (atacicept-vymj), a B-cell activating factor (BAFF) and A proliferation-inducing ligand ( APRIL) inhibitor. Vera Therapeutics is evaluating multiple diseases where the reduction of autoantibodies through inhibition of BAFF and APRIL may prove clinically meaningful. Vera Therapeutics was founded in 2016 and is based in Brisbane, California. To learn more, visit .At Vera, our values are the cornerstone of our culture and guide how we work together every day. We lead with empathy, act with an owner's mindset, demand clarity, work without fences, and execute with urgency because patients are counting on us. From how we hire and develop our people to how we advance rigorous science, we are building a team committed to transforming medicine in autoimmune diseases, starting with the kidney.

Position Summary:

We are seeking a highly skilled and motivated Senior Clinical Trial Manager to join a fast-paced and collaborative team. The Senior Clinical Trial Manager will be responsible for the day-to-day operational oversight of assigned trial(s) in accordance with the protocol, standard operating procedures (SOPs) and GCP/ICH guidelines to support successful execution of the trial within timelines, budget and with the highest quality.

Responsibilities:

• * Manage all clinical operational aspects of a global clinical trial including start-up, conduct and close out activities.
• * Monitor assigned trial for adherence to the GCP, protocol, SOPs and other key performance indicators (e.g., review of monitoring reports, study tracking tools, etc.) to ensure proper oversight of the CRO and sites.
• * Proactively identifies potential study issues/risks and recommends/implements solutions.
• * Manages CRO interactions, including sponsor oversight of operational functional activities (e.g., study management, monitoring, site management, project files) and serves as the primary CRO/vendor contact.
• * Supports the CRO to ensure quality and accurate data is generated and assists in resolving any issues (e.g., subject eligibility, deviations, etc.) .* Manages study timelines to align with corporate and cross-functional goals.
• * Contribute to the writing, review and finalization of protocols or components of clinical study reports.
• * Prepares metrics and updates for Vera management.
• * Organizes and leads clinical operational meetings.
• * Organizes and leads study team meetings.
• * Develop and maintain strong working relationships with principal investigators, key clinical opinion leaders and sites.
• * May contribute to development of RFPs and participates in selection of CROs/vendors as well as review of any CRO budgets and /or change orders.
• * Develop strong cross-functional relationships and exhibits leadership skills with counterparts to ensure efficient execution of clinical trial.
• * Ensure site and CRO adherence with SOP, applicable regulations, GCP, and ICH guidelines.
• * Contributes to the development and/or review of study plans, ICFs, site manuals, patient materials, CRF completion guidelines, system specifications, etc.
• * Attend and/or present at Investigator Meetings as needed.
• * May travel up to 30%, as needed, to support clinical development programs.

Qualifications:

• * BS or higher in life sciences or health-related field.
• * 5+ years clinical development experience and progressive experience in clinical research within the pharmaceutical or biotechnology industry.
• * Rare disease and inflammatory diseases and/or difficult enrolling study experience preferred.
• * Regulatory filing and experience with inspection readiness preferred.
• * Experienced in managing, mentoring, and developing junior staff.
• * Flexible self-starter to operate in a fast-paced start-up environment. Ability to develop out of the box solutions with limited infrastructure.
• * Experience is all aspects of clinical operations.
• * Working proficiency of GCP, ICH guidelines and FDA regulations.
• * Ability to work independently as well as collaboratively in cross-functional team environment.
• * Proficiency with MS Office (e.g., Word, Excel, PowerPoint, Outlook, Project).
• * Strong interpersonal skills with excellent oral and written communications.
• * Innovative, analytical, and extremely organized to drive projects to completion.

Vera Therapeutics Inc. is an equal-opportunity employer.Vera Therapeutics is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is$150,000—$180,000 USDAt Vera, base pay is only one part of your total compensation package. At Vera, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Vera Therapeutics also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays.