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Endpoint Clinical

Interactive response technology for clinical trials

Project Manager

Full-TimeUpdated on 10/13/2026
£45k - £55k/yr
Mid
Remote in UK
Remote
Project & Program ManagementProject Management

About the job

Requirements
  • At least 2 years of project management experience in clinical trials, RTSM/IRT, clinical supply chain, or a related life sciences or technology field.
  • At least 2 years of experience in the life sciences industry.
  • Familiarity with SQL is a plus.
  • Maintain attention to detail and quality focus.
  • Provide strong customer service.
  • Demonstrate organizational and time management skills.
  • Work effectively with professionals across a wide variety of roles.
  • Handle multiple assignments with moderate supervision.
Responsibilities
  • Serve as the primary client contact for sponsor and CRO clients for RTSM-related activities after go-live, building long-term relationships throughout each study.
  • Lead recurring client status calls and steering committee meetings; own meeting agendas, minutes, and action-item tracking.
  • Manage change control for live systems by receiving requests, assessing scope and impact, coordinating with Design/Build, QA, and Biostatistics, and driving changes through validation and deployment.
  • Own the post-go-live project plan, timeline, and RAID log for each assigned study.
  • Coordinate site and depot user provisioning, training refreshers, and access issues with Help Desk and Training teams.
  • Monitor drug-supply forecasting, inventory thresholds, and resupply strategy with clients, proactively escalating operational risks.
  • Manage protocol amendments, dosing changes, new sites or countries, and investigational product updates from client request through implementation.
  • Coordinate user acceptance testing for post-go-live system changes with clients and internal build teams.
  • Track and communicate enrollment, randomization, and supply-status metrics to clients and internal leadership.
  • Manage account financial tracking, including change-order scoping, budget tracking, and invoice coordination with clients and internal finance.
  • Lead study close-out, including final reconciliation, system decommissioning, archival, and lessons-learned reviews.
  • Advocate internally for clients and partner with Sales, Design PM, Programming, QA, and Regulatory to resolve issues.
  • Maintain audit-ready documentation in accordance with GxP, 21 CFR Part 11, and internal SOPs.
  • Assess and manage risks associated with assigned client IRT systems and change requests, making decisions and recommendations within defined project, client, and governance frameworks.
  • Complete responsibilities accurately and on time, and use available resources to support timely study delivery with clear oversight, accountability, and appropriate documentation.
Desired Qualifications
  • Previous experience working in a fast-paced, entrepreneurial environment.

About the company

Endpoint Clinical provides interactive response technology (IRT) software for clinical trials, helping life sciences companies manage drug supply, patient randomization, and visit scheduling. Its platform coordinates these trial operations through a user-friendly system that can be set up, integrated with other trial management tools, and backed by ongoing services and support. The company differentiates itself through an emphasis on ease of use, strong integration with other systems, and comprehensive customer support, including collaborations with partners like THREAD and Berlinger to offer integrated solutions. Its primary goal is to help sponsors, CROs, and academic institutions run clinical trials more efficiently, with improved transparency and regulatory compliance.

Company Size

501-1,000

Company Stage

Debt Financing

Total Funding

$1.7M

Headquarters

Raleigh, North Carolina

Founded

2009

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Simplify Jobs

Simplify's Take

What believers are saying

  • Bluefin acquisition on September 14, 2026 expands Endpoint into clinical supply forecasting.
  • Elosity R3 launched April 13, 2026 with central pharmacy and rollover tools.
  • Sri Srivatsan became CEO on March 20, 2025, sharpening execution after Arsenal’s 2024 buyout.

What critics are saying

  • Bluefin integration can distract teams through 2026, delaying unified planning-execution product delivery.
  • Medidata, Oracle, and Veeva attack Endpoint’s niche with broader clinical-cloud suites.
  • Endpoint’s buyer concentration among sponsors and CROs makes any trial-program loss material.

What makes Endpoint Clinical unique

  • Endpoint supports 2,300-plus studies across 90-plus countries with regulated RTSM delivery.
  • Elosity R3 adds natural-language AI through elo while preserving study blinding and compliance.
  • Bluefin stays RTSM-agnostic, giving sponsors planning without forcing platform migration.

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Benefits

Remote Work Options

Growth & Insights and Company News

Headcount

6 month growth

7%

1 year growth

7%

2 year growth

7%
PR Newswire
Sep 14th, 2026
Endpoint Clinical acquires Bluefin to expand into clinical supply planning technology

Endpoint Clinical has acquired Bluefin, a Boston-based provider of clinical supply forecasting and planning technology. The deal expands Endpoint into clinical supply chain planning whilst maintaining Bluefin's independence and RTSM-agnostic approach. Bluefin will operate independently and continue connecting with RTSM systems across the industry. Endpoint will support Bluefin with global project management, implementation, quality and customer support capabilities. "Clinical supply planning is becoming more complex, more connected to trial execution, and more dependent on timely intelligence," said Nagaraja "Sri" Srivatsan, chief executive officer of Endpoint Clinical. The acquisition aims to link supply plans to trial execution data, enabling teams to anticipate enrolment shifts and automate forecasting. Arsenal Capital Partners acquired Endpoint Clinical in 2024 and continues supporting the company's growth.

Veristat
Jun 15th, 2026
Veristat expands biostatistics leadership to accelerate ai-powered Drug Development in complex disease areas.

Veristat expands biostatistics leadership to accelerate ai-powered Drug Development in complex disease areas. Veristat deepens expertise with Dr. Zhaohui Su and Dr. Gil Fine, names Scott Tarrant EVP of Drug Development Advisory, and welcomes Clint Wolfe as Chief HR Officer SOUTHBOROUGH, Mass. - June 23, 2026 - Veristat(TM), a global clinical research organization (CRO) and consultancy specializing in complex studies, today announced four strategic leadership hires that advance its mission to accelerate novel therapy approvals in complex disease areas, including cell and gene therapy, oncology, and rare disease. Building on its 30-year foundation in biostatistics and its recent acquisition of the medical writing and regulatory submission business of Certara, Veristat is deepening its scientific expertise and expanding its operational leadership to meet growing client demand. Dr. Zhaohui Su and Dr. Gil Fine join Veristat's Strategic Drug Development Advisory team in biostatistical leadership roles, collaborating with Scott Tarrant, who has been named Executive Vice President of the team. In addition, Clint Wolfe joins Veristat as Chief Human Resources Officer (CHRO). After spending his early career in academia working on clinical trials at Harvard University, Dr. Su took a biostatistical leadership role at Quintiles (now IQVIA). He continued his career building biostatistical teams from the ground up at OM1 and then Ontada, McKesson's oncology technology and insights business unit. At Veristat, Dr. Su will serve as Vice President of Statistical Consulting. "I have collaborated with many great people at Veristat over the years and jumped at the opportunity to join their team full time," said Dr. Su. "I appreciate Veristat's science-first approach to clinical trials and aim to blend this axiom with my knowledge and experience building teams to get investigational drugs approved faster so patients benefit sooner." Dr. Su will be leading a Veristat webinar about real-world evidence on June 30th - learn more here. Dr. Gil Fine received his PhD in biostatistics from the University of California, Los Angeles and has spent three decades at the forefront of drug development. His career includes senior leadership roles at Syntex and SuperGen, where he led the biostatistics team for more than a decade as executive director followed by leadership roles at Astex Pharmaceuticals and Sumitomo Dainippon Pharma Oncology. He has an exceptional track record spanning NDA, MAA, BLA, and IND submissions and approvals across oncology, autoimmune disorders, pain management, and rare disease. At Veristat, Dr. Fine will serve as Biostatistical Consultant. Scott Tarrant will serve as the Executive Vice President of Veristat's Drug Development Advisory, bringing 30 years of life sciences experience. After serving in the U.S. Army Corp of Engineers, Tarrant held positions with Nalco Chemical, Therimmune, and Xceleron. At Xceleron, he helped scale U.S. operations from a start-up to a $12 million company. Most recently, Tarrant served as Chief Business Officer at RRD Biopharma Development, quickly growing the company from 15 to 50 employees. Clint Wolfe joins as Chief Human Resources Officer with more than 25 years of experience leading global teams across private equity-owned and public life sciences companies. Most recently, Wolfe served as CHRO at Neovance and Endpoint Clinical Solutions (previously part of the Fortrea Corporation). He has also held executive positions at ArisGlobal and BioClinica, and spent 16 years at IMS Health (now IQVIA). "Veristat is building on its rich foundation in statistics, established through the leadership of Drs. Su and Fine, while adding a new global leader to help grow our consulting business under Scott. We will be well-positioned to expand globally, continue leveraging AI technologies, and apply modern approaches to complex research programs across our business," said Kim Boericke, CEO of Veristat. "And Clint is a seasoned professional with a proven ability to seamlessly integrate acquired business units and teams, onboard the next generation of talent, and develop our team so we can continue delivering the highest support to our clients." About Veristat Veristat is a full-service CRO and consultancy that helps life sciences companies bring novel therapies to market fast. With 30 years of experience and support in more than 100 regulatory approvals and deep expertise in rare disease, neurological disease, oncology, and advanced therapies, Veristat integrates strategic planning, regulatory insight, and trial execution to overcome complex challenges and accelerate success. From early planning through approval, Veristat delivers tailored solutions that drive meaningful outcomes for patients worldwide. Media Contact: Lisa Barbadora, Barbadora INK for Veristat +1 (610) 420-3413 [email protected]

PR Newswire
Apr 13th, 2026
Endpoint Clinical launches Elosity R3 with AI-driven insights and enhanced clinical trial supply management

Endpoint Clinical has launched Elosity R3, a major update to its Randomisation and Trial Supply Management platform. The release introduces enhanced clinical supply operations tools, including central pharmacy management, flexible sourcing strategies and patient rollover capabilities across studies. The update expands the platform's AI capabilities through elo, which enables clinical teams to interact with RTSM and supply data using natural language whilst maintaining study blinding and regulatory compliance. Elosity R3 aims to support increasingly complex global and adaptive trials by strengthening how teams plan, manage and monitor clinical supply operations. Built on cloud-based architecture, the platform enables connectivity across clinical and enterprise systems, providing end-to-end visibility. The release is now available to sponsors and contract research organisations worldwide.

The Healthcare Technology Report
Mar 31st, 2026
Isa Grimes represents Endpoint Clinical at NYC Awards Night.

Isa Grimes represents Endpoint Clinical at NYC Awards Night. Published. March 31, 2026 At this year's NYC Awards Night, The Healthcare Technology Repo were pleased to welcome leaders across healthcare and technology who are driving innovation in patient care and clinical outcomes. Among those in attendance was Isa Grimes, VP of Global Marketing at Endpoint Clinical, a company focused on advancing clinical trial technology through interactive response systems and digital solutions. Endpoint Clinical provides interactive response technology (IRT/RTSM) that supports patient randomization and clinical trial supply management, enabling sponsors and CROs to manage dosing, drug distribution, and inventory across complex, global studies. Its platform is designed to bring greater control and visibility to trial operations, helping teams navigate protocol complexity and execute studies more efficiently. Isa brings over 20 years of experience across digital, brand, and performance marketing, with a strong track record of leading global teams and driving strategic growth. At Endpoint Clinical, he builds data-driven go-to-market strategies that increase pipeline contribution and support revenue growth, while enhancing the company's visibility and differentiation within the eClinical space. It was a pleasure having Isa join The Healthcare Technology Repo in New York and represent Endpoint Clinical at this year's event. Picture: Isa Grimes at NYC Awards Night.

PR Newswire
Dec 1st, 2025
Endpoint Clinical Named a Leader in Everest Group's 2025 Life Sciences RTSM Products PEAK Matrix(R) Assessment

Endpoint Clinical named a Leader in Everest Group's 2025 Life Sciences RTSM Products PEAK Matrix(R) Assessment. News provided by. Dec 01, 2025, 17:09 ET RALEIGH, N.C., Dec. 1, 2025 /PRNewswire/ - Endpoint Clinical has been recognized as a Leader in the 2025 Everest Group Life Sciences Randomization and Trial Supply Management (RTSM) Products PEAK Matrix(R) Assessment. This distinction reflects Endpoint Clinical's commitment to advancing clinical research through innovative RTSM solutions that prioritize reliability, flexibility and patient-centric outcomes. The Everest Group PEAK Matrix(R) is a proprietary framework that evaluates providers based on two critical dimensions: market impact and vision and capability. Market impact considers factors such as adoption, portfolio diversity and value delivered to clients, while vision and capability assess strategy, technology innovation, flexibility, engagement models and support services. Endpoint Clinical's leadership position underscores its passion for patients and the privilege of supporting sponsors and CROs across multiple geographies, phases and therapeutic areas. With decades of experience powering thousands of studies, Endpoint delivers RTSM solutions designed for speed, quality and agility, helping to bring life-saving therapies to market. Guided by a customer-first approach, Endpoint provides tailored services and responsive support to ensure every trial runs smoothly and efficiently while continuing to innovate with AI-driven capabilities that enhance decision-making, optimize trial operations and improve outcomes for patients worldwide. "Being recognized as a Leader by Everest Group validates our dedication to bringing innovation in clinical trial operations through our technology, people and exceptional service," said Nagaraja Srivatsan, CEO at Endpoint Clinical. "Our focus remains on providing solutions that combine high quality, speed and agility to ultimately improve outcomes for both patients and sponsors." For more information about Endpoint Clinical's RTSM solutions, visit https://www.endpointclinical.com. To review the report, including details on Endpoint Clinical's Leader status, please visit: https://www.everestgrp.com/report/egr-2025-72-r-7726 About Endpoint Clinical Endpoint Clinical is a trusted clinical trial technology and service partner that delivers reliable RTSM solutions. Endpoint blends seamlessly into clinical trial processes by providing anticipatory and adaptive solutions to proactively mitigate risks. With decades of experience, Endpoint offers a deep understanding of the challenges sponsors and CROs face. Its tech-forward dedication to innovation and high-touch services enables Endpoint to control the controllables and proactively generate speedy, strategic solutions so sponsors and CROs can focus on running seamless clinical trials. SOURCE Endpoint Clinical