Manager, Clinical Operations

Iota Biosciences

$120K — $150K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a scientific field
  • 8+ years of clinical research experience in medical devices or 5+ years with an advanced degree
  • Track record of building and managing clinical operations teams
  • In-depth understanding of clinical operations, GCP, and US regulations
  • Experience with global clinical studies, particularly in EU or APAC
  • At least 2 years of monitoring experience
  • Familiarity with Class III medical device clinical studies

Responsibilities

  • Lead and mentor a high-performing clinical operations team
  • Manage clinical execution plans including protocols and budgets
  • Oversee all phases of clinical trial activities from start-up to close-out
  • Direct CROs and manage vendor relationships
  • Collaborate with hospitals and KOLs involved in clinical studies
  • Support post-clinical activities and product market launches
  • Coordinate with cross-functional teams to align clinical and regulatory goals

Benefits

  • Comprehensive health coverage, 100% covered for employees and families
  • Quality dental and vision coverage
  • Onsite gym access in Alameda
  • Generous vacation pay
  • Paid parental leave
  • Flexible work schedule options
  • Annual bonus plan
  • Long-term incentive plan (LTIP)
  • 401(k) plan with employer match
Full Job Description
The Role

We are seeking a Manager of our Clinical Operations team, to provide leadership in the oversight, management, planning, coordination, and execution of clinical projects. This is a highly hands-on role for someone who wants to impact company development through effective and efficient management of clinical operations staff and activities.

This role is ideal for someone who has experience in global Class III active implantable medical device studies, who can manage teams and vendors efficiently and effectively, and who wants to help bring a unique product to market for an underserved patient population.

What You'll Do
  • Manage a high performing clinical operations team by providing direction, subject matter expertise, training and mentorship.
  • Responsible for managing the design, development, modification, and evaluation of clinical execution plans (e.g., protocol, case report forms, consent forms, source document worksheets, budget, timelines, gap analysis, etc.)
  • Accountable for the comprehensive clinical trial activities including but not limited to study start-up, site activation, site management, vendor oversight, study reports, site and study close-out.
  • Provide technical direction to clinical research organizations (CROs) and oversee vendor selection/management as needed to execute clinical studies.
  • Work closely with hospitals and investigators participating in clinical studies and maintain close working relationships with KOLs, other investigating physicians and site coordinators
  • Provide input and support for post-clinical activities and market launch of products.
  • Establish / support cross-functional teams to ensure optimal alignment of Clinical, Regulatory, commercial goals, site operations, data monitoring and review, and safety surveillance and reporting expectations.
  • Ensure clinical research programs are conducted in accordance with company standard operating procedures (SOPs), Good Clinical Practice (GCP), and applicable regulations.


What we're looking for
  • Bachelor's degree in a scientific field
  • Minimum 8+ years of relevant clinical research experience in the medical device field, or an advanced degree with a minimum of 5 years of relevant experience in the medical device field
  • Proven success building and managing clinical operations teams
  • Comprehensive knowledge of clinical operations including Good Clinical Practices and all applicable US regulations
  • Experience with global clinical studies (e.g., EU or APAC regions)
  • At least 2 years monitoring experience
  • Experience with Class III medical device clinical studies
  • Effective verbal and written communication skills
  • Organized, self-motivated, ability to effectively manage multiple projects and priorities; high attention to detail
  • Must be a strong team player and effectively interface with other departments including translational medicine, regulatory, quality, product development


Preferred Qualifications
  • Clinical research certification (e.g., CCRP, CCRA, etc)
  • Experience with site and sponsor FDA BIMO inspections
  • Superior problem-solving skills.
  • Experience with urology clinical studies
  • Effective interpersonal/communication skills


What makes this role unique:
  • Innovation - first of its kind device that will require a unique clinical study design.
  • Build & Lead - you'll bring clinical operations expertise to the department and have the opportunity to influence department strategy and implementation
  • Impact - clinical studies are a critical part of product development. Your work here will directly influence time to market and providing a new therapy to an underserved patient population.


iota offers a very competitive benefits package that includes the following:

Health & Wellness
  • Comprehensive health coverage for you and your family, covered at 100%
  • Access to quality dental and vision coverage
  • Onsite Gym in Alameda


Work-Life Balance
  • Generous vacation pay
  • Paid parental leave
  • Options for flexible work schedules


Competitive Compensation
  • Annual Bonus Plan
  • Long Term Incentive Plan (LTIP)
  • 401(k) plan with employer match

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