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Home Flexible Job Board Head of Partnerships

Salary Unstated 93d ago

Head of Partnerships

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Kivo

Boston, MA, US

Full-time Permanent Remote

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Summary

The Head of Partnerships will build and lead Kivo's partner ecosystem across software vendors and service providers to create integrated solutions. This role involves sourcing, structuring, and executing partnerships while collaborating with the C-suite to shape go-to-market motions.

Job Description

About Kivo

Kivo is the modern document management and workflow platform for emerging and scaling life sciences companies. We give drug development companies a single regulated system of record and system of action — combining eTMF, regulatory document workflows, and quality processes in a platform built for the realities of small and mid-size sponsors.

Our customers are clinical-stage biotechs, CROs, and the partners that support them. As we scale, we are investing in a partner ecosystem of services firms, technology vendors, and integration partners that extend Kivo's value across the broader clinical and regulatory stack.

We are hiring a Head of Partnerships to build and own that ecosystem.

About the Role

The Head of Partnerships will lead Kivo's partnerships strategy across software vendors (CTMS, EDC, RIM, QMS, safety, and adjacent platforms) and service providers (CROs, regulatory consultancies, quality consultancies). You will be responsible for sourcing, structuring, and executing partnerships that produce integrated, differentiated solutions for our shared customers — and for identifying the next set of markets and verticals where Kivo should compete.

You will work directly with Kivo's C-suite, Sales, and product leadership to shape go-to-market motion, influence the roadmap based on partner and market signal, and represent Kivo externally with senior leaders at services firms, software companies, and industry organizations.

What You'll Do

• Build and own Kivo's partner program across service providers and software vendors, from strategy through signed agreement and ongoing relationship management.

• Lead the development of integrated solutions with software partners (CTMS, EDC, RIM, QMS, safety, and adjacent categories), including commercial structure, joint positioning, and integration scope in partnership with our product team.

• Establish and grow referral and co-sell relationships with CROs, regulatory consultancies, and quality consultancies serving emerging and mid-size biotechs.

• Represent Kivo at industry events, partner forums, and customer-facing conversations, building a strong external presence in the clinical and regulatory operations community.

• Partner closely with sales, marketing, and product to ensure partnerships translate into pipeline, revenue, and customer outcomes — not just logos on a slide.

• Develop the operating cadence, metrics, and infrastructure for the partner function as Kivo scales.

What We're Looking For

Required

• 10+ years of business development, partnerships, or strategic alliances experience in life sciences SaaS software.

• Direct working experience in at least one of the following categories: regulatory information management (RIM), quality management systems (QMS), trial master file (TMF), or other clinical operations software (CTMS, EDC, eISF, safety, etc.).

• Strong working knowledge of the CRO landscape and the clinical trial market — including how sponsors, CROs, and technology vendors interact across study conduct and submission.

• Track record of sourcing, negotiating, and closing partnership agreements that produced measurable commercial outcomes (pipeline, revenue, retention, or integrated product value).

• Comfort operating in a startup environment: building from a blank page, prioritizing ruthlessly, and moving between strategy and execution without losing momentum.

• Excellent executive presence and written communication — you can credibly represent Kivo to a CRO COO, a software CEO, or a head of regulatory at a clinical-stage sponsor.

Nice to Have

• Experience in adjacent regulated markets — medical devices, diagnostics, pre-clinical/discovery, or CDMO/CMC.

• Familiarity with eCTD, ICH guidelines (E6, M11, etc.), 21 CFR Part 11, EU Annex 11, or other GxP regulatory frameworks.

• Prior experience standing up a partner program from scratch, including building the underlying playbooks, contracts, and operating cadence.

• Existing relationships across CROs, regulatory consultancies, and life sciences software vendors.

• Experience evaluating new market entry and influencing product strategy based on partner and customer signal.

Why Kivo

• Work closely with the leadership team and have direct influence on the company strategy, roadmap, and go-to-market.

• Modern product in a market dominated by legacy incumbents — a real opportunity to win on architecture, speed, and customer experience.

• Strong existing customer base of emerging and scaling biotechs, and an active product investment in headless and integrated access (MCP, structured action handoff) that makes integrated partner solutions genuinely differentiated.

• Competitive compensation, meaningful equity, and benefits.

• Remote-friendly, with regular in-person collaboration and industry travel.

About the company

Kivo

Kivo is building the infrastructure for GxP compliance in the era of AI-powered drug development. Its unified cloud platform supports Regulatory, Clinical, and Quality operations — including RIM, eTMF, QMS, controlled document management, submission assembly, eCTD lifecycle management, inspection readiness, SOP management, and training management — within a single, audit-ready environment. With Part 11-compliant e-signatures, role-based permissions, continuous validation assurance, and a lossless data model that preserves context from legacy systems, Kivo gives life sciences teams the compliant foundation to reduce operational friction and accelerate time to market.

Clinical Capabilities:
eTMF - Electronic Trial Master File
TMF Transfer & Migration
Trial Archiving / Long Term Storage
Active CRO Trial Management
Vendor Management
Inspection Preparedness & Readiness

Regulatory Capabilities:
RIM - Regulatory Information Management
eCTD - Electronic Common Technical Document
Submission Assembly
Document Templates
Project Management
Registration Management
Dossier Management

Quality Capabilities:
QMS - Quality Management System
CAPA Management
Vendor Audit
SOP Management
Training

Founded

2021

Company size

11-50 employees

Industry

Software Development

Org type

Privately Held

Headquarters

Portland, Oregon

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About the company

Kivo

Kivo is building the infrastructure for GxP compliance in the era of AI-powered drug development. Its unified cloud platform supports Regulatory, Clinical, and Quality operations — including RIM, eTMF, QMS, controlled document management, submission assembly, eCTD lifecycle management, inspection readiness, SOP management, and training management — within a single, audit-ready environment. With Part 11-compliant e-signatures, role-based permissions, continuous validation assurance, and a lossless data model that preserves context from legacy systems, Kivo gives life sciences teams the compliant foundation to reduce operational friction and accelerate time to market.

Clinical Capabilities:
eTMF - Electronic Trial Master File
TMF Transfer & Migration
Trial Archiving / Long Term Storage
Active CRO Trial Management
Vendor Management
Inspection Preparedness & Readiness

Regulatory Capabilities:
RIM - Regulatory Information Management
eCTD - Electronic Common Technical Document
Submission Assembly
Document Templates
Project Management
Registration Management
Dossier Management

Quality Capabilities:
QMS - Quality Management System
CAPA Management
Vendor Audit
SOP Management
Training

Founded

2021

Company size

11-50 employees

Industry

Software Development

Org type

Privately Held

Headquarters

Portland, Oregon

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