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Bicara Therapeutics

Senior Project Manager, Clinical Operations

RemoteUnited States only
Published
Role
Project Management
Experience
Senior
Employment
Full-time
Company size
Mid-size
$176k–$206k/yr
Check eligibility

Open to US only. Set where you work from to check your eligibility.

No BS summary

Senior Project Manager with 5+ years industry experience (≥3 years project management) in biotech/pharmaceuticals, ideally oncology clinical trials. Based in Boston (willingness to travel 10–15%). Must know project planning/tracking, risk management, and ICH/GCP guidelines.

Core skills

project planningrisk management

Required skills

project trackingbudget monitoringinvoice managementaccrual trackingclinical study plan developmentversion trackingteam training

Optional skills

oncology clinical trials experienceICH/GCP knowledge

What you'll do

  • 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.

What they require

  • 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 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.
  • Ability to work independently in a fast-paced, results-driven, highly accountable environment; ability to prioritize and manage multiple tasks.
  • Willingness to travel up to 10-15% of the time.

Benefits

  • Equal opportunity employer; encourages diverse applicants

clinical-stage biotech company pioneering bifunctional antibodies for targeted tumor modulation

🇺🇸 United StatesBiotechMid-size
$176k–$206k/yr