Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
Responsible for strategy and oversight for assigned clinical research studies, as well as the overall relationship for a specific client. Responsible for overall cross-functional leadership of assigned project(s)/program and project/program team(s) to ensure delivery within specified budgets and timelines and in accordance with applicable regulatory guidelines/requirements, Tempus Compass Standard Operating Procedures (SOPs) and project specific instructions. Independently oversees the execution of assigned clinical research studies under a specific sponsor/client, applying and providing guidance to client and team members on best practices tailored to the applicable project, patient population, drug product or device (if applicable) and client project/program goals and objectives. The Director, SPCR will have regular interactions with key internal and external stakeholders to discuss project status, escalate issues, and troubleshoot inquiries. This role is expected to build and maintain positive rapport and working relationships with internal and external project team members, broader stakeholders and executive leadership. Strong written and verbal communication skills in English, operational leadership, and decision-making, ability to delegate, strategic thinking, conflict resolution, clinical project management experience and attention to detail are required. The role is primarily responsible for operational study strategy and study execution, and client relationship management.
Job Responsibilities:
Working as Director, Strategic Partnerships & Client Relationship tasks may include but are not limited to:
Develop and execute strategic partnership initiatives to grow client portfolios and enhance long-term client satisfaction, retention, and expansion
Serve as the primary point of contact for a key client and their projects, ensuring high levels of engagement, trust, and retention
Collaborate with clinical operations, project management, and executive leadership to align service delivery with client expectations
Understand client objectives and ensure they are translated effectively across project teams
Lead cross-functional project and program teams to manage the development and execution of program strategy in alignment with corporate goals
Have accountability as the primary contact for the client program, including ownership, maintenance, and communication of all program information, including strategy, scope, deliverables, timelines, status and key risks
Identify new business opportunities with assigned client(s) and support proposal development in collaboration with the Commercial Operations and Business Development teams
Monitor client satisfaction and implement strategies to proactively address concerns or performance gaps
Represent Tempus Compass at industry conferences, client meetings, and strategic forums
Stay informed on clinical research trends, regulatory changes, and competitive landscape to advise clients and internal stakeholders
Contribute to, interface with, or lead different levels of study governance, as required
In conjunction with functional area leads and sponsor, recommend, implement and oversee operational strategies as well as risk management plans inclusive of the Risk Assessment Categorization Tool (RACT)
Oversee the development of applicable study specific plans across a program including critical path activities and interdependencies for assigned clinical stud(ies)
Oversee the assigned project(s)/program scope of work and associated contractual agreements including recognizing and negotiating changes in scope in collaboration with Project Manager/Clinical Study Manager and Commercial Operations throughout the project lifecycle from start-up to close-out
Collaborate with clients to proactively provide win/win solutions
Lead cross-functional teams and third parties/vendors to ensure effective teamwork and communication
Oversee and analyze project deliverables including timeline, quality, scope, and financials
Leverage input from all critical functions to define critical path activities/decisions and associated risks, in collaboration with project/program teams, to ensure the projects/program meet their milestones on time and on budget
Oversee resource needs throughout the project/program lifecycle including ensuring that project tasks are correctly assigned to team members and vendors
Oversee and coordinate internal team members working on assigned project(s)/program as required
Mentor and lead project/program teams
Manage team dynamics and provide feedback on project team members’ performance to the project team member and respective line management
Contribute to business development initiatives, including proposals, responses to RFIs, and bid defense presentations as needed
Contribute to Tempus Compass initiatives as needed
Line manage - onboard, mentor and oversee Project Managers/Clinical Study Managers assigned to project(s) for assigned key client(s) as needed
Demonstration of Tempus Compass Values:
Consistently strives to demonstrate the following Tempus Compass values:
Recognizes that the team is always stronger than the individual
Seeks to inspire others by demonstrating consistently strong performance
Treats people with respect regardless of role or point of view
Listen well and seek to understand before reacting
Provides candid, helpful and timely feedback to colleagues
Demonstrates curiosity about and contributes effectively to areas outside of their specialty
Keeps the bigger picture in mind when making decisions
Never stops learning
Questions assumptions and offers suggestions for improvement
Focuses on results rather than process and seeks to minimize complexity when process is required
Identifies and addresses root causes, not symptoms
Demonstrates poise in stressful situations
Strives to always do the right thing
Questions actions that are incongruent with Tempus Compass values
Minimum Qualifications:
University/college degree with preference in a health or life science field from an appropriately accredited institution, advanced degree preferred
Minimum of ten (10)+ years relevant clinical research experience with five (5)+ years in a client-facing or strategic partnership role in a combination of research site, biotech or pharma, or CRO experience
Minimum of five (5)+ years Project Management experience at a CRO
Proven ability to build and maintain successful relationships and to effectively communicate at senior management level
Highly effective communicator at all levels with both clients and internally. Must be open and direct with strong oral and written communication skills
Proven track record of developing and maintaining high-value strategic partnerships
Exceptional communication, negotiation, and interpersonal skills
Ability to work cross-functionally and influence at all levels of the organization
Strategic thinker with a client-first mindset and an eye for innovation and growth
Strong understanding of the clinical trial lifecycle and regulatory landscape
Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of drug development programs, or of ISO Guidelines and GCP including US regulatory requirements for devices
Demonstrated ability to handle multiple competing priorities and to utilize resources effectively
Demonstrated ability to build rapport with team members and clients
Excellent written and verbal communication skills
Excellent organization skills, attention to detail and ability to handle multiple competing and changing priorities within tight timelines
Able to proactively anticipate needs and follow through on all assigned tasks
Proficient in Google for Business products including but not limited to GMail, GDrive, Google Documents, and Google Sheet. Proficient in Microsoft Office products including but not limited to Word, Excel, PowerPoint, and Sharepoint
Proficient in project management tools and processes (Smartsheet, Financial management systems)
Ability to travel overnight (up to 20%)
Preferred Qualifications:
PMP (Project Management Professional) Certified
Cell Therapy experience
Oncology clinical trial experience
Early phase oncology clinical trial experience
Diagnostics experience
IDE trial experience
Observational trial experience
Global Project Management experience
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Illinois Pay Range: $170,000-$210,000
The expected salary range above is applicable if the role is performed from California and may vary for other locations (Colorado, Illinois, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.
Additionally, for remote roles open to individuals in unincorporated Los Angeles – including remote roles- Tempus reasonably believes that criminal history may have a direct, adverse and negative relationship on the following job duties, potentially resulting in the withdrawal of the conditional offer of employment: engaging positively with customers and other employees; accessing confidential information, including intellectual property, trade secrets, and protected health information; and appropriately handling such information in accordance with legal and ethical standards. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
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