Senior Project Manager, Clinical Operations at Bicara Therapeutics

Boston, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

04 Sep, 26

Salary

206000.0

Posted On

06 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Management, Clinical Operations, Risk Management, Budget Monitoring, Cross-functional Leadership, ICH/GCP Guidelines, Oncology Clinical Trials, Strategic Planning, Stakeholder Management, Analytical Thinking, Problem Solving, Communication Skills, Detail Oriented, Vendor Management, Audit Preparation, Clinical Study Planning

Industry

Biotechnology Research

Description

Bicara Therapeutics is seeking a Senior Project Manager to provide project management expertise and strong operational support and leadership to the team. The role is highly cross-functional with key interactions with internal and external stakeholders. In partnership with the Clinical Operations Team, the Project Manager will assist in developing integrated plans and will understand developing strategy, identifying critical path activities and determining risks / mitigation plans. The successful candidate will have strong communication skills. They will be highly organized, detail oriented, comfortable with ambiguity, and have a proven track record of managing and driving projects. The role will report to the Senior Director, Clinical Operations. This role is based in our Boston office and follows a hybrid schedule, with three in-office days each week. Responsibilities · Serve as an integral part of the Clinical Operations core team to drive operations efficiently including generating integrated project plans, identifying and tracking key project milestones and metrics, and monitoring budgets, invoices, and accruals. · Provide cross-functional transparency of the clinical trial(s) progress to ensure team is efficiently progressing forward with deliverables, including deliverables from CRO and other partners. · Organize internal and external meetings (development of agendas, minutes, and presentations) · Manage ancillary supplies for clinical trials · Support risk management including risk assessment, mitigation planning, and internal and external audit preparation and follow-up · Contribute to development of clinical study plans and manuals, including version tracking and team training. · Provide support to senior leadership in deﬁning the deliverables on the clinical trial(s) which coincide with the expectations deﬁned in the departmental and company goals. · Maintain ongoing communication with team members and all stakeholders including senior leadership and external partners or vendors. · Foster a sense of inclusion and create a shared sense of purpose. Qualifications · Bachelor’s degree in life sciences or a related ﬁeld required · A minimum of 5+ years of industry experience with a minimum of 3+ years of project management in the biotech/pharmaceutical industry. Preference for experience in oncology clinical trials with solid knowledge of ICH/GCP and related guidelines and regulations. · Strong experience in project management techniques and principles including, but not limited to, project planning, execution and tracking, and risk identiﬁcation and management. · Strong organizational and leadership skills, including demonstrated ability to maintain a high level of productivity and inﬂuence at all levels of an organization. · Strong analytical, problem solving and critical thinking skills, including an ability to combine attention to detail with a big picture perspective. · Excellent oral and written communication skills, including presentation and facilitation skills, to effectively inform key updates and issues across to senior leadership and to all levels of the organization, as needed. · Ability to work independently and successfully in a fast-paced, results-driven, highly accountable environment with large potential impact; ability to prioritize and manage multiple tasks simultaneously, integrate cross-functional issues, and balance competing priorities effectively. · Willingness to travel up to 10-15% of the time. Company Overview Bicara Therapeutics is a clinical-stage biotech company pioneering bifunctional antibodies for targeted tumor modulation. Founded in 2020, we've built a global team of over 100 employees headquartered in Boston, with a clear focus on advancing our lead asset, ficerafusp alfa, or FICERA - a potentially first-in-class bifunctional EGFR-directed antibody combined with a TGF-β ligand trap. Our innovative approach combines tumor-targeting with tumor modulation, where one arm localizes to the tumor while the other serves as a modulator, designed to deliver superior efficacy, improved safety, and enhanced durability directly at the tumor site. FICERA specifically addresses a key challenge in solid tumor treatment by enabling immune cell penetration into tumors, reducing fibrosis and immunosuppression while reversing TGF-β-driven resistance mechanisms - ultimately designed to drive the deep, durable responses that may translate into better outcomes and survival for patients. For more information, please visit www.bicara.com. Here at Bicara, we believe in building diverse teams and cultivating a culture where all voices are included. We encourage people from all backgrounds to apply. Bicara Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.

Responsibilities

The Senior Project Manager will drive clinical operations by developing integrated project plans, tracking milestones, and monitoring budgets. They will provide cross-functional transparency and manage risks and deliverables in collaboration with CROs and internal stakeholders.