clinical research associate bridge program

Define your future in clinical research 

Benefits of cra drive, cra academ y, success stories, drive  entry points, clinical research associate drive:  program overview, who is eligible for cra drive, recent graduates, established clinical professionals, about  our cra academy program, cra academy program highlights, dedicated six weeks of training, ongoing support and development, successful results, award winning recognition, future leaders, elevated performance , hear from our colleagues, “after graduating, i was more grounded in the knowledge and application of clinical research tenets, could identify my strengths and felt empowered to reach out to my trainers and peers.” , “they truly care about my career goals and where i want to be, and they motivate me to meet those goals.” , “i was promoted to ctm in october 2019, with the same customer who accepted me as a brand-new cra. it has been an incredible opportunity, and i have learned a lot. i love the cra role.” , “what a huge contribution to the organization, bringing all these talented people into our workforce, while offering them great growth opportunities.”, start your story today. become a cra with the world leader in serving science. if you’re enthusiastic and committed to success, here are three roles to consider. each role lends to your potential of becoming a cra., clinical trial coordinator (ctc), country approval specialist (cas), assistant clinical research associate (acra).

Industry-Bridging Programs

“Your transition to industry is guaranteed with Clueo Clinical Signature Industry-Bridging Programs TM “.

Clinical Trial Assistant IBP

Study Start-Up Specialist IBP

Clinical Research Coordinator IBP

Clinical Research Associate IBP

How industry-bridging programs work.

You can kickstart your clinical research industry career in 3 simple steps with our all-in-one IBP program. Click on each step below to explore more details.

Complete our career quiz to find the industry job that matches your strengths, personality, and aspirations.

Click on the name of the program that matches your chosen industry career. e.g., CRA-IBP for CRA role.

Clueo Clinical Industry-Bridging Programs (IBPs)

You will have access to comprehensive career support services, and resources to help you navigate the job market and securing employment post-training such as:

• Personalized guidance on career goals and aspirations
• Customized advice on industry-specific job search strategies
• Individualized resume and cover letter assistance
• Targeted interview preparation and coaching
• Ongoing support and feedback for career development
• Networking tips and strategies for industry connections
• Assistance in showcasing relevant skills and experiences
• Guidance on professional development opportunities within your desired career
• Assistance in creating a personalized career plan to fast-track your career goals

Why Choose Us?

• Customized Training Programs:  We specialise in transforming candidates with limited experience into competent industry professionals clinical trials.
• Industry-Relevant Curriculum:  Our curriculum reflects current industry trends, tools, technologies, and skills relevant to the evolving job market.
• Expertise and Experience:  Benefit from our extensive expertise in the industry.
• Flexible and Interactive Learning:  Learn from anywhere, at anytime, and acquire hands-on, practical learning experiences that bridge the gap between theory and real-world application.
• Comprehensive Career Support Services:  Access comprehensive career support services, including job placement assistance, resume writing, career counselling, and resources to help you navigate the job market and securing employment post-training.
• Guaranteed industry job:  Access to full career support until you secure paid employment upon successful completion of our program.
• On-the-Job Support:  You have two years to finish the program, which includes on-the-job support once you entered the industry to enable you to gain confidence to navigate job responsibilities independently and effectively.
• Affordable and Accessible:  Benefit from training programs that offer competitive pricing, and instalment plans to help individuals seeking professional development without a significant financial burden.
• Industry-Recognized Certification:  Gain certifications that are recognized in the industry, adding value to your resume and increasing your marketability.
• Proven Track Record:  We have a proven track record of success, demonstrated by the achievements and career advancements of our past participants. Check out the testimonials and feedback from past participants and clients who have successfully benefited from our training programs.

Student intake per enrolment period is limited and competitive to maintain only top quality candidates enter the industry and to ensure that each trainee’s individual needs are adequately met to boost their industry-transition success.

[email protected] | 1300 39 22 06

Privacy Policy | Terms and Conditions

Copyright © 2020- Clueo Clinical Pty Ltd | ABN 26 639 212 150

CRA I - CRA Bridge Program

• Location: United States
• Categories Clinical Monitoring
• __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions
• __vacancyopjusttionswidget.opt-Remote Working __ Remote

TA Business Partner

• Icon Strategic Solutions

Send me a message

About the role, this vacancy has now expired. please see similar roles below....

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

This role will focus on Phase l-lll  therapeutic area of (vaccines).

What do you need to have?

• Undergraduate degree or its international equivalent in clinical, science, or health related field from an accredited institution; a licensed healthcare professional (i.e., registered nurse); or equivalent work experience required
• 2+ years of clinical monitoring experience or equivalent combination of education and experience is required for the level 2 role; 5+ years is required for a level 3
• Knowledge of ICH and local regulatory authority regulations regarding drug 
• Experience in monitoring all trial components (PSSV to COV)
• Ability to travel as needed (greater than 40%)

To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.

Benefits of Working in ICON: Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

ICON and you

ICON history

Career Pathways

Benefits & Rewards

Environmental, Social & Governance

Women in IT

Application process

Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.

Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.

One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.

Day in the life

Teaser label

Content type

Publish date

To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

Unlocking your Potential: The Benefits of ICON’s EPIC Internship Program  Internship programs have become a vital stepping stone for students and young professionals seeking to gain practic

Read more about ICON plc's EPIC (Entry-level Professionals in CRO (Contract Research Organization)) internship program.

How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce

 Senior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.

Press play to find out more

Similar jobs

Clinical Monitoring

Remote Working

Business Area

ICON Strategic Solutions

Job Categories

Description

As a Senior Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be partnering with one

2023-103968

Expiry date

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech

2023-104179

As Clinical Research Associate (CRA), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.  A CRA is a professional who cont

2023-103904

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

2023-106051

Baltimore, United States

United States

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us

2024-109470

2024-109462

Browse popular job categories below or search all jobs above

CRA Careers at IQVIA

Help tackle healthcare’s greatest challenges to improve patient health.

Not ready to apply? Join our Global Talent Network .

Put your passion to work

IQVIA Clinical Research Associates play a vital role in the evolution of clinical development. They bring passion, ambition, and a deep level of expertise to help solve complex clinical issues while ensuring adherence to regulations and sponsor requirements. Here, you'll find the autonomy and flexibility you need to take your CRA career to the next level.

Choose your path

Sponsor-dedicated.

When you join as a sponsor-dedicated CRA, you’ll embrace the stability of a global contract research organization and harness the power of industry-leading technology. As part of this alignment, you'll gain valuable experience, working side by side one of our pharmaceutical customers, and expand your knowledge in a wide variety of therapeutic areas.

Our sponsor-dedicated model brings together the right people, experience and ideas to deliver high quality solutions specific to the customer’s needs.

Full-service

When you become a CRA as part of our full-service alignment, you'll embrace your passion for a specific therapeutic area and support a variety of sponsors. With access to world-class training and cutting-edge technology, developed specifically for IQVIA CRAs, you'll have the resources you need to create the career you want.

Our full-service model delivers cutting-edge clinical research through state-of-the-art innovation.

IQVIA Biotech

When you pursue a CRA career with IQVIA Biotech, you'll work directly with customers in a collaborative environment to help change the face of biotech. Using your extensive therapeutic knowledge, you’ll oversee uniquely-focused clinical studies, where you’ll be exposed to pioneering protocols and experience a dedicated partnership with your team like none other.

IQVIA Biotech is at the forefront of clinical trials in a variety of therapeutic areas through the delivery of flexible solutions within the biotech sector.

IQVIA empowers you to drive your own path within the organization. As no person's route is the same and the clinical research landscape is forever changing, you are encouraged to continually seek career growth opportunities and align your interests with your career goals.

Senior Clinical Research Associate 2

At IQVIA, we are committed to supplying our CRAs with the right tools, training and development support to allow for success and career growth. In addition to the rewarding work, collaboration and engaged line management, there is a constant focus on development as your career growth supports also the growth of the company.

Director, Clinical Operations

For me, it’s the people and knowing I’m making a difference in creating a healthier world that inspire me to come to work every day. I can go to anyone with a challenge, and they are willing to help. Together, we’re thinking outside of the box to navigate each sites’ unique needs and challenges.

Senior Clinical Research Associate

Explore unlimited opportunities

Clinical Research Associates can leverage their experience in a variety of ways that enable them to pursue their unique passions. Whether you choose to advance within a specific therapeutic area or want to explore something new, you can create the career you want. Explore the various career opportunities when you join IQVIA as a CRA.

What you can expect

All CRAs at IQVIA, regardless of alignment, thrive within our dynamic culture and experience:

Professional Development

Work-Life Balance

Supportive Leadership

Best-in-Class Training

Collaboration

Explore clinical monitoring jobs.

• R1416182 Senior Clinical Research Associate, Sponsor dedicated in POLAND Learn more Multiple Locations
• R1388858 Senior Clinical Research Associate (m/w/d), Single Sponsor Learn more Multiple Locations
• R1416180 Clinical Research Associate, Single Sponsor dedicated in POLAND Learn more Multiple Locations

Join our Global Talent Network

Let’s stay connected. Sign up to receive alerts when new opportunities become available that match your career ambitions.

Job Category Select a Job Category Administrative Support Advanced Analytics Client Services Clinical Data Management Clinical Operations Clinical Project Management/Leadership Clinical Trial Supply & Logistics Connected Devices Consulting Contract Management Database Management Systems Finance Human Resources Information Security Internships IT Design & Development IT Infrastructure IT Support Lab Science Lab Science Advisors Lab Services Laboratory Laboratory Projects Legal and Regulatory Lifecycle Safety Marketing Medical Medical Affairs Medical Communications Medical Sales & Services Monitoring Patient Centric Services (PCS) Phase 1/Clinic Operations Product Support (Tier 3) Production Project and Program Management QA & Testing Quality Assurance Sales Sales Support Software Development Engineering Statistician Strategic Supplier Services Strategy and Corporate Development Technical Writing

Remote Select... Yes

Areas of Interest

Confirm Email

Search for a location and select one from the list of suggestions. Select a job category from the list of options. Finally, click “Add” to create your job alert. Multiple job alerts may be created by repeating these steps.

Explore life at IQVIA

• Global Careers
• China Careers
• Japan Careers

I’m working toward a better future for patients. And I do it

Search Jobs

Radius: Enter distance 5 15 25 35 50

Begin your Clinical Research Associate ( CRA) career with Parexel

Helping the clinical research industry and the individuals breaking into it.

If you have completed a minimum of a Bachelor’s degree in Life Sciences, Pharmaceuticals, Clinical Research or Nursing and are interested in kick-starting your CRA journey, learn more on how to join the other 250+ individuals across the Americas and EMEA who have completed the program. When applying to our APEX Program, our hiring process will entail a CV review, screening of qualifications, interviews and a post assessment selection.

Programa APEX CRA

El Programa acelerado de educación, exposición y experiencia para monitores de investigación clínica (Accelerated Program of Education, Exposure, and Experience for Clinical Research Associates, APEX CRA) proporciona formación básica en investigación clínica, incluida la experiencia en proyectos y sistemas, a nuevos CRA contratados que son recién graduados universitarios con menos de un año de experiencia en monitoreo.

Si tienes título universitario en Ciencias de la Salud, Farmacia, Investigación Clínica, Enfermería o carreras afines, y te interesa iniciar tu carrera laboral como CRA, lee sobre cómo unirte a nuestro equipo de más de 250 personas en América y EMEA que han completado el programa. 

Al postularte a nuestro Programa APEX, el equipo de contratación hará un análisis de tu perfil a través de la revisión de tu CV, entrevistas, y evaluaciones adicionales.

Why the APEX CRA Program

We are a leading contract research organization with over 20,000 employees globally. For more than 40 years, we’ve assisted clients in the pharmaceutical, biotechnology, and medical device industries simplify their journey to market. We take our work personally, we do it with empathy and we're committed to making a difference. A nd together, we’re doing it  With Heart ™.

#1 CRO in Phase I clinical research and customer loyalty in the delivery of Phase II/III services

3,000+ project staff worldwide with Oncology/Hematology experienc

250+ Decentralized ClinicalTrials (DCTs)

Hear from graduated participants

How did the APEX Program help prepare you to become a CRA?

Diego Teraza: Fall 2022 Program

What impressed you about the APEX CRA Program?

 Olivia Perry: Fall 2022 Program

What did you enjoy most about the program?

Mimi Nguyen: Spring 2022 Program

Explore Parexel

Our Culture

Explore what makes Parexel's work culture unique

Emerging Talent

Begin your career journey at Parexel

Hiring Process

Find out what to expect when applying to Parexel.

Sign up for our Talent Community

Sign up and we’ll reach out with job alerts when positions that match your career interests become available. We’ll also share periodic updates about the latest company news and events.

• Core Curriculum
• Web Seminars
• On-Boarding Programs
• On-Site Training
• On-Demand eLearning Courses
• Web Seminar Archives
• CCAD Programs
• GCP Training Assessments
• Mock Audits Findings Based Training
• Virtual Meetings Support Services
• Customized eLearning Solutions
• Licensing of Barnett's Content
• SOP Development Training
• Acquisition Integration
• Training Subscription
• Publications
• Course Catalog

• Training Courses
• GCP Training & Assessments
• Audits and Mock Inspections
• Licensing of Barnett's Content
• SOP Development & Training

10-Week CRA & CRC Beginner Program

Upcoming Courses

Monday Afternoons. No class May 27, July 1.

Resume support is available as an add-on option! Click here for more details.

Wednesday Evenings.

Modal body text goes here.

Course Description

The online 10-Week CRA & CRC Beginner Program provides a comprehensive introduction to clinical research and the job functions of the Clinical Research Associate (CRA) and Clinical Research Coordinator (CRC) for drug, biologic, and device trials. This program is geared toward individuals seeking a new career or career change into clinical research, but haven’t decided which job track to pursue. Case studies and industry best practices are presented to emphasize how the learning objectives apply directly to the responsibilities of the CRA and CRC.

The resources required to take this on-line course are already at your fingertips - an Internet connection and a phone. After registering, you will receive an email confirmation that provides you with the Web Seminar link and audio connection information.

Prior to the start of the course, participants will receive Module 1 materials. Course materials for subsequent modules will be sent weekly prior to class. Come to class prepared to interact – you will be able to ask questions, provide feedback and participate in discussions and group work. Upon course completion, participants will be provided training certificates. In order to receive accreditation CEUs, participants are required to pass both a mid-term and final exam. Upon completion of the exams, CEU certificates will be provided.

Learning Objectives

• Describe and discuss the investigational product development process, including FDA regulations, ICH guidelines, and Good Clinical Practice (GCP)
• Explain the roles and responsibilities of a CRA and CRC
• Describe the four types of monitoring visits, including the responsibilities of the CRA and CRC in preparation, activities, and follow-up
• Explain the Key Pre-Study Concepts: Role of the Principal Investigator, Site Selection, Clinical Trial Agreement and Budget Negotiation
• Discuss the role of the Institutional Review Board in clinical trials, define informed consent requirements, and discuss the informed consent process
• Discuss the study site initiation, interim monitoring activities, and data management
• Define safety definitions and reporting requirements for both drugs and devices
• Examine accountability for the investigational product and study closeout visits
• Discuss regulatory compliance and quality assurance as it relates to audits and inspections

Course Outline

• Module 1: Investigational Product Development, the FDA, and Good Clinical Practice Guidelines
• Module 2: Clinical Research Team: Roles and Responsibilities
• Module 3: The Principal Investigator, Site Selection, and Budget Negotiation
• Module 4: Clinical Study Protocol Elements
• Module 5: Institutional Review Boards, the Consent of Human Volunteers, and HIPAA
• Module 6: Study Monitoring, Data Management, and Study Initiation Visit
• Module 7: Safety Reporting: Definitions and Reporting Requirements
• Module 8: Accountability for the Test Article and Trial Termination Visits
• Module 9: Regulatory Compliance and Quality Assurance: Audits and Inspections
• Module 10: Managing Your Time and Preparing for the Interview

Who Should Attend

• Aspiring Clinical Research Associates and Clinical Research Coordinators (This course is also appropriate for Clinical Research Associates and Clinical Research Coordinators with less than six months of experience)
• College Students and New Graduates in a Scientific Field

NOTE: This course is for individual registrants only and does not allow for group training.

What participants say about Barnett's 10-Week courses ...

“Great course! Instruction is expertly led and engaging. I will recommend Barnett to any colleague and will seek out topics for my own future training and professional development needs.”

"The course has been so incredibly helpful thus far...I look forward to Thursday evenings!"

“This class exceeded my expectations of an online learning experience. The instructor was knowledgeable, came equipped with great examples to keep the class interesting and is a strong presenter. Thank you!”

The course will be led by one of the following instructors:

Nikki Christison, B.S., C.C.R.A., T.I.A.C.R.

Susan Torchio, R.N., B.S.N.

Elizabeth Weeks-Rowe, LVN, C.C.R.A.

Click here for complete trainer biographies

Course Length and Time

10 weeks for 3 hours each week.

Registration Fees

$1,795 by Early Bird Deadline

$1,995 after Early Bird Deadline

This course is for individual registrants only and does not allow for group training.

All participants are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met.

Accreditation Information

Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education.  Participants will receive 30 hours (3.0 CEUs) of continuing education credit for full participation, including the completion of a mid-term exam, final exam, and program evaluation.  Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion.  ACPE#: 0778-0000-23-002-L99-P. Released: 1/23.

Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.