Clinical Research Associate

US-Anywhere
+ 5 other locationsRemote
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s degree in Life Sciences or equivalent, or RN qualification
  • 2+ years of on-site monitoring experience in clinical research
  • Experience with early development Phase I/II studies in multiple therapeutic areas
  • Proficient in ICH-GCP and local regulatory requirements
  • Familiarity with clinical systems like CTMS and eTMF
  • Strong communication skills and problem-solving ability
  • Willing to travel up to 60% across the Midwest region.

Responsibilities

  • Act as the main liaison between investigation sites and the sponsor
  • Conduct various site visits: selection, initiation, monitoring, and close-out
  • Ensure compliance with ICH-GCP, SOPs, and applicable regulations
  • Maintain current documentation in clinical trial management systems
  • Support site staff training and compliance record maintenance
  • Monitor patient safety and manage adverse event reporting
  • Assist in subject recruitment and retention at the site level
  • Oversee drug accountability and manage storage/return/destruction processes
  • Resolve data queries and ensure accurate data entry
  • Document site progress and escalate risks to the clinical team
  • Track site budgets and ensure timely site payments if applicable
  • Collaborate with cross-functional teams including CTAs and CTMs.

Benefits

  • Comprehensive total rewards package for health and wellbeing
  • Health coverage including medical, dental, and vision
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training.
Full Job Description
Clinical Research Associate - Early Development Multi Therapeutic - Midwest Region
What you will be doing:

  • Serve as the primary point of contact between investigation sites and the sponsor

  • Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out

  • Ensure site compliance with ICH-GCP, SOPs, and regulations

  • Maintain up-to-date documentation in CTMS and eTMF systems

  • Support and track site staff training and maintain compliance records

  • Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting

  • Support subject recruitment and retention efforts at the site level

  • Oversee drug accountability and ensure proper storage, return, or destruction

  • Resolve data queries and drive timely, high-quality data entry

  • Document site progress and escalate risks or issues to the clinical team

  • Assist in tracking site budgets and ensuring timely site payments (as applicable)

  • Collaborate with cross-functional partners including CTAs, LTMs, and CTMs

You are:

  • A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RN

  • Eligible to work in United States without visa sponsorship

  • A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry

  • Experienced monitoring early development Phase I/II clinical studies, across multiple therapeutic areas

  • Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF

  • A clear communicator, problem-solver, and collaborative team player

  • Willing and able to travel up to 60% for on-site monitoring visits across the Midwest region; preference given to candidates residing in Midwest region near major HUB airports to support efficient regional travel


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our to read more about the benefits ICON offers.

About Pharmaceutical Research Associates, Inc

Pharmaceutical Research Associates, Inc Careers

Joining Pharmaceutical Research Associates, Inc presents an unparalleled opportunity to become part of a leading team in the pharmaceutical research industry. This company stands as a beacon of innovation, leadership, and professional growth.

Explore Job Opportunities

Pharmaceutical Research Associates, Inc is actively seeking skilled professionals eager to impact the world of pharmaceuticals and healthcare. With a variety of job opportunities available, candidates can find positions that match their skills and career ambitions perfectly.

Experience the Culture and Benefits

At Pharmaceutical Research Associates, Inc, the culture thrives on diversity, innovation, and a commitment to employee growth. The company offers comprehensive benefits designed to support the health, well-being, and financial security of each team member. From diversity training to leadership programs, employees are equipped with resources to thrive both professionally and personally.

Internship Programs

For those starting their career journey, Pharmaceutical Research Associates, Inc provides robust internship programs. These opportunities allow interns to work alongside experienced professionals, gaining invaluable industry insight and enhancing their resume through practical, hands-on experience.

Professional Growth and Development

Career advancement is a cornerstone of employment at Pharmaceutical Research Associates, Inc. The company supports career growth through professional development programs, networking opportunities, and leadership training, ensuring that every team member has the tools to succeed.

Innovative Work Environment

Pharmaceutical Research Associates, Inc is at the forefront of pharmaceutical innovation. The team is dedicated to pioneering research that leads to new discoveries and solutions in healthcare, offering employees a chance to contribute to meaningful projects that push industry boundaries.

Join the Team

Pharmaceutical Research Associates, Inc is hiring! Search open positions that align with your professional skills and interests. The company values curious, creative, and solution-driven team players ready to drive success in the pharmaceutical industry.

Stay Connected

Keep up to date with career tips, industry insights, and more from Pharmaceutical Research Associates, Inc. Subscribe to receive personalized job alerts and the latest news, tailored to your professional interests and career goals.

Apply Now

Ready to take the next step in your career? Explore the positions available, tailor your resume, and prepare for an interview with Pharmaceutical Research Associates, Inc. Discover how your expertise can contribute to the global impact of this dynamic company.

READ CAREERS BLOG

Job Alert Emails

Personalize your subscription to receive job alerts, latest news, and insider tips tailored to your preferences. See what exciting and rewarding opportunities await at Pharmaceutical Research Associates, Inc.
Learn more about Pharmaceutical Research Associates, Inc

Similar Jobs

More Jobs at Pharmaceutical Research Associates, Inc

More Pharmaceuticals & Biotech Jobs

Find similar Clinical Research Associate jobs: