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APEX Clinical Research Associate (CRA) - October 2026 Cohort

Role overview

Qualifications

  • Minimum Bachelor’s degree in life sciences/data sciences/pharmacy or other health related disciplines.
  • Up to 24 months maximum experience in clinical research.
  • Strong interpersonal, written, and verbal communication skills within a matrixed team.
  • Strong computer skills with aptitude to learn new systems quickly.

Responsibilities

  • Support CRAs and Clinical Operations Leads with project tasks.
  • Conduct observational and co-monitoring support on-site or during remote visits.
  • Manage site quality and delivery from site identification through to close-out.
  • Address and resolve site issues and questions.

Key facts

Other skills

  • Communication
  • Social Skills
  • Computer Literacy
  • Teamwork
  • Time Management
  • Physical Flexibility

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.

Do you have up to 2 years of experience working in Clinical Research and do you have experience in these preferred therapeutic areas: Oncology, Cell & Gene Therapy, Ophthalmology, or Dermatology

AND

Do you live in the West or Central Regions of the US (California, Washington, Idaho, Michigan, Texas, Nevada, Arizona, New Mexico, Colorado or Illinois) 

*Currently hiring for October Cohort – Candidates must be available to start on October 12, 2026

**Must be able to also attend in-person training in Raliegh, NC the week of November 9, 2026, if hired **

APEX CRA: The Accelerated Program of Education, Exposure, and Experience for Clinical Research Associates (APEX CRA) provides foundational clinical research training including project and system experience. 

As they progress through the program, APEX CRAs perform billable project tasks to support the CRAs and Clinical Operations Leads (COLs) with a focus in three developmental areas: Project Support, Initiation CRA support, and Site Facing support. They are required to complete the ACRP Entry Level Knowledge Assessment (CRKA) and are enrolled in a 1-year membership to the ACRP.

APEX CRAs work closely with CRAs to gain exposure to and experience with the CRA role and its responsibilities across a period of four months. They get the opportunity to practically apply in-class concepts with day-to-day application by working with clinical systems including Clinical Trial Management Systems (CTMS), Electronic Data Capture, Safety Information Systems, and TMF platforms. Instructor-led trainings are supplemented with ongoing coaching and support of Line Managers and COLs. 

APEX CRAs accompany CRAs for observational and co-monitoring support on-site or during remote visits which combines learning for the APEX CRAs and workload aid for their CRA colleagues. Upon completion of the program, APEX CRAs are well-positioned to independently function within the CRA role and to immediately begin successful monitoring.

At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they’re set up for success. As the clinical sites’ sole point of contact, this includes addressing and resolving site issues and questions. You’ll also manage site quality and delivery from site identification through to close-out.

Travel expectations: The CRA role is a largely field based role that requires frequent travel multiple times per month. Investigator sites participating in studies span the country, from large research centers to smaller offices, so traveling to them is a part of the CRAs role. You can expect at least five (5) minimum visits per month and 7 days on site which might require weekly overnight travel and some travel on weekends in different locations. Travel time can vary widely depending on the location of the site, flights, proximity to the airport and travel delays. In addition, there are other factors that will impact the travel times including your location, the study you are working on and the location of the sites. During the first six months, travel will be limited but, as your development continues, traveling will increase.

Job Qualifications:

  • Minimum Bachelor’s degree in life sciences/data sciences/pharmacy or other health related disciplines.
  • Up to 24 months maximum experience in clinical research
  • Strong interpersonal, written, and verbal communication skills within a matrixed team.
  • Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
  • A client-focused approach to work and flexible attitude with respect to assignments/new learning.
  • The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
  • An honest and ethical work approach to promote the development of life changing treatments for patients.
  • Strong computer skills with aptitude to learn new systems quickly.
  • Ability to travel 80% of the time
  • Candidates must be able to legally work in the US without the need for sponsorship now or in the future
  • Spanish or French language capability considered beneficial.

Parexel is proud to be a leading Clinical Research Organization with colleagues across the globe. As a member of our team, you’ll get to know your coworkers on a personal level. Have a question? A clinical research leader, project team member, technology “super user” or collaborator are a phone call away. Our clinical research teams meet regularly to have discussions in an open environment, allowing our team members to share their expertise and promote learning within the team. Management supports and encourages career growth through consistent performance discussions and evaluations. Whether your interest is to progress into a more senior level CRA role, into line management, Quality, Project Leadership or a variety of other positions, Parexel prides itself on career opportunities for our employees.

The Potential base Pay Range for this role is: $60k-$70k. The actual salary offered may vary within the range based on a number of factors including position/level offered, skills, education, training, experience, professional achievement, and location.

Some roles may also be eligible for additional incentives, bonuses, and other benefits. Our talent acquisition team will provide additional details on bonus plan or incentive programs for those eligible roles. We offer benefit programs including paid time off, 401k match, life insurance, health insurance, and other benefit offerings in accordance with the terms of applicable plans to all eligible employees.

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

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