Director, Solutions Onboarding

Posted 2 Days Ago
Be an Early Applicant
5 Locations
In-Office or Remote
187K-205K Annually
Expert/Leader
Cloud • Healthtech • Information Technology
The Role
Lead and manage a team delivering hands-on platform training and onboarding for Faro customers. Translate clinical development workflows into effective training, develop self-service training artifacts, beta test features with user feedback, and drive customer enablement to ensure independent platform use. Periodic travel for meetings and onsite trainings required.
Summary Generated by Built In

Faro aims to improve lives by helping life sciences companies answer complex clinical questions, simply, efficiently and effectively. Our software platform is used to orchestrate complex clinical development with a single source of truth. It brings words, data and teams together, empowering researchers to design more intelligent trials, master complexity and reach milestones faster.

The Director, Solutions Onboarding leads a team of onboarding specialists and data associates with a clear mission: delivering hands-on platform training that empowers customers to use the Faro Platform independently and to its full potential. This role is focused on training and enablement. You will draw on a strong clinical background to understand customer workflows and translate them into effective training experiences, ensuring customers develop the skills and confidence to operate the platform on their own.

Duties and Responsibilities
  • Leverage deep understanding of clinical development from protocol design and development to trial execution to ensure training sessions are contextually relevant and resonate with customer end users across a variety of therapeutic areas and study designs
  • Lead workshops with customer user groups (Clinical Scientists, Clinical Operations, Data Management, and Medical Writers) with a focus on end user training for self-sufficiency, empowering customers to independently leverage the Faro Platform
  • Develop and maintain training and self-service artifacts for clients based on how they will use the software; working with the Product Experience team for consistency across client enablement
  • Beta test new platform features from the end user lens and provide structured feedback to the Product team to inform the roadmap, leveraging your professional clinical trial experience to draw conclusions in context of using the Faro solutions
  • Manage and develop a team of Solutions Onboarding Specialists/Managers, who deliver platform training and support customer onboarding and adoption; and Data Associates, who support the accurate configuration and labeling of clinical content within the Faro Platform
  • Role is expected to require periodic travel for team and all-company meetings, and to customer sites for trainings/workshops as requested by customers.

RequirementsQualifications
  • Bachelor’s degree required, preferably in physical or life science or statistics discipline
  • 10+ years of experience in clinical research or drug development, with sufficient protocol-level knowledge to understand and contextualize customer workflows; prior experience as a Clinical Scientist, Clinical Program Manager, Study Manager, CRA, CTM, or Data Manager at a sponsor, CRO, or clinical site is preferred
  • Experience designing or delivering clinical training programs or user enablement initiatives; familiarity with instructional design principles is a plus
  • Demonstrated ability to create externally facing, end-user system training artifacts (e.g., user guides, how-to videos, quick reference cards, FAQ documents) and directly train end users on software platforms
  • 5+ years experience managing teams
  • Familiarity with clinical trial technologies (e.g., EDC, IRT, CTMS, ePRO, eCOA, eConsent, TMF) and regulatory requirements, sufficient to understand and contextualize customer workflows during training 
Skills and Competencies
  • Strong organizational, motivational, and leadership skills, promoting a team-based approach
  • Strong attention to detail skills and ability to triage and aid in resolution of escalations
  • Ability to work independently in a group setting; ability to adjust to changing priorities
  • Excellent team player with demonstrated track record of success in a cross-functional team environment; consistent commitment to delivering on team goals with a sense of shared urgency
  • Strong emotional intelligence, interpersonal and communication skills, both verbal and written
  • Strong organizational and leadership skills
  • Strong problem-solving skills
  • Strong facilitation and instructional communication skills; ability to translate complex clinical concepts into accessible training materials for diverse end users
  • Goal-oriented
  • Ability to project and maintain a professional and positive attitude

BenefitsSalary
  • Salary range for this position is $187,000 - $205,000
  • Salary listed reflects the base salary only and does not include other elements of total compensation
  • Individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training

Equity 

In addition to this position's salary (listed above), equity will be a major component of the total compensation for this position. We aim to offer higher-than-average equity compensation for a company of our size, and communicate equity amounts at the time of offer issuance. 

Benefits 

  • Health Care Plan (Medical, Dental & Vision)
  • Retirement Plan (401k)
  • Life Insurance (Basic)
  • Short Term and Long Term Disability
  • Paid Time Off (Flexible Vacation Policy; Paid Sick & Public Holidays Observed)
  • Training & Development Reimbursement
  • Remote Work Environment
  • Peer-to-peer bonus program
  • Company/department outings and events
  • Stock Option Plan
  • Office On-Premises Amenities; gym, restaurant tenant discount, Padel Nine

Skills Required

  • Bachelor's degree (preferably in physical or life science or statistics)
  • 10+ years of experience in clinical research or drug development with protocol-level knowledge
  • Prior experience as Clinical Scientist, Clinical Program Manager, Study Manager, CRA, CTM, or Data Manager at a sponsor, CRO, or clinical site
  • Experience designing or delivering clinical training programs or user enablement initiatives
  • Familiarity with instructional design principles
  • Demonstrated ability to create end-user system training artifacts and directly train end users on software platforms
  • 5+ years experience managing teams
  • Familiarity with clinical trial technologies (EDC, IRT, CTMS, ePRO, eCOA, eConsent, TMF) and regulatory requirements
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The Company
HQ: San Diego, CA
36 Employees
Year Founded: 2019

What We Do

Faro Health is bringing clinical trials into the digital age by helping teams manage and balance the complexity of modern trial designs through a cloud native platform. The Faro platform enables study teams to design complex clinical trials using small modular building blocks and combines that with data driven insights to orchestrate and automate operationally complex trials. Faro brings balance, centricity and flexibility to protocol development through automation and integration to downstream systems and vendors, ensuring they are always up to date and correctly configured. As a result, clinical trials using Faro are operationally efficient which avoid delays due to ambiguity and generate data that can be trusted.

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