Job description
RQM+ is The MedTech CRO, accelerating innovation to patient impact. Our tailored solutions deliver regulatory and quality expertise, FDA-recognized laboratory services, clinical trials, and reimbursement strategies across device types and therapeutic areas to bring life-changing technologies to patients — faster, safer, better.
We don’t make MedTech. We make MedTech happen.
Our experienced teams are cohesive, collaborative, and proactive, constantly seeking to improve and evolve while remaining laser-focused on customer success. RQM+ elevates the MedTech experience through best-in-class service and clear, concise communication. We serve as an extension of our customers establishing and maintaining excellent client and site relationships and providing direct access to our technology platforms for real-time data and study transparency
The Principal Proposal & Contract Strategist is a subject matter expert (SME)-level role responsible for shaping and executing enterprise-level governance across proposals and contracts. This role serves as a critical partner to Sales, Finance, Legal, and Operational leadership, providing strategic oversight, driving cross-functional alignment, and enabling commercial scalability. The Principal Strategist will lead the development of core P&C frameworks, oversee high-impact client engagements, and guide transformational initiatives that elevate the function’s performance and visibility across the organization.
Primary Responsibilities:
Proposal Management
Lead the full proposal lifecycle for strategic and complex RFPs/RFIs from intake to delivery.
Act as a strategic advisor on bid positioning, pricing logic, and commercial risk during the proposal phase.
Coordinate internal input from subject matter experts across BD, Finance, Legal, and Operations.
Guide the creation of high-quality, client-tailored proposal responses aligned with business strategy.
Shape and maintain governance of reusable content, pricing models, and intake workflows.
Monitor and analyze proposal KPIs (cycle time, win rate, SLA compliance) and recommend improvements.
Contract Management
Draft, review, redline, and negotiate strategic agreements including:
Clinical Trial Agreements (CTAs), Confidentiality Agreements (NDAs/CDAs)
Master Service Agreements (MSAs), Investigator Agreements, SOWs, and vendor contracts
Resolve complex contract issues in partnership with Legal, Finance, and Operations leadership.
Contribute to enterprise-wide template redesign and commercial contract policy updates.
Ensure compliance with internal controls, approval workflows, and regulatory standards.
Governance & Strategic Leadership
Design and evolve proposal and contract governance frameworks across the organization.
Lead cross-functional working sessions to define RACI, SLAs, and intake-to-delivery workflows.
Provide mentorship to team members across all P&C levels, drive training for new tools and processes.
Collaborate on the design and implementation of pricing tools and data models for commercial use.
Serve as P&C lead in enterprise transformation workstreams and strategic client solutioning efforts.
Legal & Regulatory Compliance
Apply expert-level understanding of contract law principles and international clinical trial regulations.
Monitor and interpret compliance standards: FDA, GCP, HIPAA, GDPR, Sunshine Act, EU MDR, ISO 14155.
Translate evolving legal/regulatory requirements into actionable contract and proposal strategies.
Requirements:
- Bachelor’s degree in Business Administration, Life Sciences, Law, or related field (required)
- Advanced degree or certifications (e.g., IACCM, NCMA, APMP) preferred
- 10+ years in contract research, medical device, or life sciences with increasing responsibility in proposals/contracts
- Demonstrated experience leading governance, pricing strategy, or cross-functional commercial initiatives
- Strong knowledge of contract research budgets, risk frameworks, and regulatory environments
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), especially Excel for pricing analysis
- Experience with Contract Lifecycle Management (CLM) systems (e.g., DocuSign CLM, Ironclad)
- Familiarity with Salesforce, proposal software, CTMS platforms, and eTMF systems
- Expertise in supporting global trials, including EU MDR and international contracting standards
- Ability to translate data into actionable performance insights for continuous improvement
Behaviors:
- Strategic Thinking, Business Acumen, Decision Quality, Integrity & Trust, Collaboration, Customer Focus, Process Management, Change Agility, Influence, Planning
Supervisory Responsibilities:
- This position does not have direct reports but may serve as a mentor and process lead across team initiatives.
Work Environment/Physical Demands:
- This role operates in a professional virtual office environment. Routine use of computers, phones, and other standard equipment is expected. This role may occasionally require lifting or moving materials up to 25 pounds.
Being an industry leader in Medtech is just the beginning for RQM+. We consider our employees our biggest asset and we invest heavily in ongoing learning and development. Providing a rewarding place to work is rooted deep in our core values. From an industry leading compensation package to a deeply engrained focus on work life balance, RQM+ has a unique offering for regulatory and quality professionals. At RQM+, you are not just another employee, you are a member of RQM+ family. Make your impact today!
We invite you to apply if you have an interest in learning more about our organization and beginning your journey with us.
Job Opportunity Verification
At RQM+, we prioritize the security of our job applicants. To ensure a safe application process:
All legitimate RQM+ job opportunities are listed on our official careers page: rqmplus.com/careers
Every candidate going through the interview process will participate in a voice and/or video interview.
Exercise caution with unsolicited job offers or requests for sensitive information.
