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Director​/Sr. Director, Clinical Operations Lead

Job in Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: Valid8 Financial, Inc.
Full Time position
Listed on 2026-08-13
Job specializations:
  • Management
    Operations Management, Project & Program Management, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 120000 - 200000 USD Yearly USD 120000.00 200000.00 YEAR
Job Description & How to Apply Below

Paratus is decoding evolution to discover and develop first-in-class medicines for serious diseases where today’s therapies fall short. We are a global team of drug hunters dedicated to transforming nature’s most resilient traits into first-in-class medicines. Our interdisciplinary teams combine AI-powered discovery with deep drug development expertise to translate these insights into differentiated therapeutic programs .

This is an opportunity to be the founding clinical operations leader at a company where your work will shape both the science and the organization.

Position Overview:

As Paratus Sciences' first dedicated clinical operations hire, you will own the end-to-end delivery of our clinical pipeline. This is not a role for a process follower, it is a role for a dynamic builder and operator who can translate a clinical development strategy into executable programs, establish the infrastructure that scales with us, and lead with equal parts strategic judgment and hands-on accountability.

You will be the operational backbone of our most critical near-term milestones across two pipeline programs. You will define how we work with CROs, how we govern our vendors, how we manage risk, and how we build the team that carries us through Phase 2 and beyond.

This role reports to the Head of Clinical Development and is initially an individual contributor position with an opportunity to build and scale the clinical operations team as the pipeline advances.

This position is based in Boston, Massachusetts , with an expectation of working in the office a minimum of two days per week. Flexibility to work across global time zones is required .

Role

Description:

Study Execution & CRO Governance
Lead the full lifecycle of clinical trial execution from CRO and vendor selection, through contracting, study startup, site management oversight, and study close-out. Own the sponsor-side CRO relationship across the current pipeline, including our lead Phase 1 FIH program (healthy volunteers and patients) and the next program advancing toward IND and FIH, with accountability for timelines, budgets, and quality standards.

Assess study feasibility, develop cost estimates, and provide input into contracts, work orders, and change orders in support of outsourcing decisions.

Create and execute clinical operational strategic plans aligned with product strategy and resource allocation, translating developmentobjectivesinto executable, resourced program plans.

Operational Infrastructure
Build the clinical operations foundation Paratus will scale on: SOPs, vendor qualification frameworks, oversight plans, and a risk-based monitoring approach. You will establish practices that are fit-for-purpose today and structured to grow as the pipeline expands.

Budget & Finance Partnership
Manage clinical trial budgets and forecasts across programs. Partner closely with Finance on accruals, variance analysis, and program-level cost accountability. Proactively flag risks before they become surprises.

Risk Management & Program Momentum
Develop and execute risk mitigation strategies that protect program timelines. Represent clinical operations in cross-functional program discussions ; serving as the operational voice on timelines, risks, trade-offs, and decisions.

Team Building
Identify, recruit, and develop the Clin Ops team as the pipeline scales including CTMs, CRA oversight, study managers, and beyond. Model a high-performance culture that is inspection-ready, compliant, and mission-driven.

Regulatory & Quality Compliance
Ensure all studies are executed in accordance with ICH-GCP, FDA/EMA regulatory requirements, and internal SOPs.

Qualifications:

10+ years of clinical operations experience in biotech or pharma, with direct sponsor-side CRO management experience

Demonstrated track record leading early phase trials, including FIH and Phase 1/2 studies;

Proven ability to manage CROs and cross-functional clinical programs end-to-end from vendor selection through study close-out

Deep command of ICH-GCP, FDA/EMA regulatory requirements, and global clinical trial execution

Working proficiency with clinical systems (CTMS, eTMF, EDC) and their role in study quality

Stro…

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