Senior Director/Executive Director, Clinical Operations
Company: Rakuten Medical Inc. - US
Location: San Diego
Posted on: October 29, 2024
Job Description:
Position Summary
Reporting to the Senior Vice President of Clinical Development, the
Senior Director/Executive Director of Clinical Operations will be a
key leader with responsibilities to manage all clinical operations
in coordination with other leadership at the company. This is an
excellent opportunity to join a rapidly growing company that is
well funded to advance novel cutting-edge anticancer therapies into
registration trials and later commercialization.
The candidate will function as the product Global Study Team Leader
to plan, organize, and coordinate all operational aspects of a
global multi-regional clinical study from protocol development
through database lock while ensuring timelines for different
regions are fulfilled.
The Senior Director/Executive Director will be a roll-up of the
sleeves to get the job done team member, work with a sense of
urgency, with attention to details, and work with utmost integrity
in a fast-paced small biotech environment.
The ideal candidate will have at least 10 years of experience
leading clinical trial operations including multinational/multisite
clinical studies with experience in oncology drug development. The
candidate will have strong leadership skills with ability to be
hands-on and drive execution and manage the clinical team.
Experience with clinical development of combination drug/device
therapies is a plus.
Key Duties and Responsibilities
- Align with the SVP of Clinical Development for successful
implementation of studies. Responsible for management of compounds
at the program and franchise levels including supporting at the
Portfolio Design Committee.
- Lead Clinical Research Organizations (CRO)/Vendor selection
process for outsourced activities, including developing an RFP,
managing the bidding process, analysis of proposals, budgets, and
leading and documenting vendor selection decisions. Includes review
of Scope of Work, budgets and negotiating contracts through
execution in a timely manner.
- Chair or participate in global meetings or conference calls
with multi-disciplinary study team across multiple time
zones/countries/regions, regional monitors, or vendors (e.g., CROs,
central Labs).
- Coordinate activities with other functional groups, such as
Regulatory, Drug Safety, Biostatistics, Supply Chain, etc.
- Work with CROs to define and ensure the coordination of Sponsor
and CRO responsibilities, obligations are being met in a timely
manner.
- Lead the team developing critical study documents, including,
but not limited to study protocols, informed consent form
templates, various management plans and study trackers.
- Lead global timelines and budget management to optimize
achievement of study goals and milestones.
- Provides leadership, effective management and guidance to the
Clinical Operations group.
- Develops and continually improves departmental infra-structure
including development of SOPs, work practices, training and
workshops and ensuring inspection ready state of clinical
operations activities.
- Ensures that clinical trials are properly resourced, managed
and executed within budget and in accordance with established
timelines.
- Ensures clinical trials are conducted in compliance with
relevant SOPs, regulatory requirements, Good Clinical Practice and
the highest quality standards.
- Evaluates data quality and study progress on an ongoing basis,
informs management of potential issues and works with the team on
corrective action plans. Drives solid departmental and study
budgeting practices collaborating with Finance.
- Oversees the selection and management of CROs, clinical
consultants, and vendors and may serve on the Governance and
Oversight Committees.
- Ensures appropriate maintenance of clinical trial master files
and documents.
- Responsible for representing Clinical Operations on
cross-functional project teams for strategic planning, risk/benefit
assessments and achievement of company, project and team
goals.
- Provides leadership for Clinical Operations related issues and
advise management team of potential issues and solutions.
- Manages, mentors and develops staff in order to maximize their
capabilities and contributions to the organization. Provides clear,
motivating and constructive feedback.
- Must be able to travel up to 20% of time on average, may be
higher in accordance with company and/or program
requirements
- Maintain strong relationships with site study personnel to
ensure site engagement.
- Other duties as assigned
Desired Education, Skills and Experience
- BS degree or higher in science, health or related field (MS
degree preferred)
- Minimum 12 years relevant industry experience in
clinical/medical research or pharmaceuticals/medical
devices
- Minimum 10 years relevant experience managing projects and
working with clinical professionals within a team, as well as
working in a cross-functional product development setting
- Global Oncology and drug/device combination experience
preferred
- Experience in CRO selection and management including drafting
requests for proposals (RFPs), bidding process, vendor negotiations
etc.
- Strong organizational/prioritization of multiple tasks under
tight timeframes with close attention to detail in a global
environment.
- Excellent communication and interpersonal skills.
- Excellent computer skills.
- Advanced degree desired.
Travel Requirements:
- Ability to travel 25% domestically and international travel
The expected salary range for this position based in California is
$200,000 to $250,000 annually. Actual pay will be determined based
on experience, qualification, geographic location, and other
job-related factors. Company is posting role confidentially.
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Keywords: Rakuten Medical Inc. - US, Placentia , Senior Director/Executive Director, Clinical Operations, Executive , San Diego, California
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