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Site Activation Leader

Role overview

Qualifications

  • 4–7 years in clinical research operations, including site activation leadership
  • Strong understanding of clinical trial start-up processes and timelines
  • Bachelor’s degree in Life Sciences, Healthcare, Business, or related field
  • Proven experience managing site activation activities and teams

Responsibilities

  • Lead site activation strategy and execution for assigned clinical studies
  • Oversee all start-up milestones from feasibility through site activation
  • Guide and mentor site activation team members
  • Serve as the Study Start-Up (SSU) subject matter expert for assigned clients

Key facts

  • Remote from: United States
  • Full time
  • Senior (5-10 years)
  • English

Other skills

  • Strategic Planning
  • Problem Solving
  • Communication
  • Analytical Thinking
  • Detail Oriented

About the company

Parexel logo

Parexel

Contract Research Organizations (CRO)

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size10001

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Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Site Activation Leader

We are seeking a highly driven Site Activation Leader to join our Site Activation Center of Excellence. In this role, you will lead the planning, execution, and oversight of site activation across clinical trials—ensuring studies are initiated on time, within scope, and to the highest quality standards.

You will play a critical role in accelerating clinical research by driving efficient site start-up activities from feasibility through activation across multiple studies and therapeutic areas. We are focusing on hiring an individual on the west coast for this position.

What You’ll Do:

Site Activation Leadership & Strategy

  • Lead site activation strategy and execution for assigned clinical studies

  • Oversee all start-up milestones from feasibility through site activation

  • Develop and manage study critical path plans, including regulatory and operational activities

  • Identify risks, proactively mitigate delays, and ensure delivery timelines are met

  • Drive cross-functional problem solving to resolve complex activation challenges

Team & Stakeholder Leadership

  • Guide and mentor site activation team members

  • Act as a key liaison between project management, start-up teams, and stakeholders

  • Communicate activation progress, risks, and solutions to internal teams and leadership

  • Collaborate with clinical operations to align with study objectives

Client Engagement & Business Support

  • Serve as the Study Start-Up (SSU) subject matter expert for assigned clients

  • Provide strategic guidance and best practices for study initiation

  • Support proposal development and bid defense activities

Process Improvement & Quality

  • Implement standardized processes and best practices across studies

  • Analyze metrics to drive continuous improvement and operational efficiency

  • Ensure compliance with regulatory requirements, SOPs, and GCP

  • Contribute to process, template, and documentation development

Systems & Reporting

  • Leverage CTMS, EDC, IXRS, and TMF systems to optimize workflows

  • Ensure data integrity and accurate documentation across studies

  • Develop reports, metrics, and insights for leadership decision-making

What You Bring:

Experience

  • 4–7 years in clinical research operations, including site activation leadership

  • Proven experience managing site activation activities and teams

  • Strong understanding of clinical trial start-up processes and timelines

  • Experience working with study sites, investigators, and regulatory requirements

Skills

  • Advanced project management and strategic planning capabilities

  • Strong knowledge of GCP and clinical trial regulations

  • Proficiency with CTMS, EDC, IXRS, and TMF systems

  • Excellent communication and stakeholder management skills

  • Ability to manage multiple complex projects and priorities

  • Strong analytical thinking, problem-solving, and attention to detail

Education

  • Bachelor’s degree in Life Sciences, Healthcare, Business, or related field

  • Additional training in clinical operations or project management is a plus

Why Join Us?

  • Work remotely with a global, collaborative team

  • Play a critical role in advancing clinical research and patient outcomes

  • Opportunity to lead complex, high-impact studies across therapeutic areas

  • Be part of a team committed to operational excellence and innovation

EEO Disclaimer
Parexel is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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