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Parexel

End-to-end clinical trials and regulatory consulting

Research Associate

Clinical Research OperationsConfirmed live in the last 24 hours
Part-timeBaltimore, MD, USA

About the Job

Requirements

  • Proven customer service experience in a fast-paced environment.
  • Background working in a medical or clinical setting.
  • Comfort with prolonged periods of standing and walking.
  • A Bachelor of Science or higher in a related life science field, or a high school diploma or GED with relevant experience.
  • Availability for at least 16 hours per week and two 12-hour weekend shifts in a four-week month, or three 12-hour weekend shifts in a five-week month.
  • Ability to work any shift, including day, evening, overnight, and weekend shifts.
  • Ability to work 40 hours per week during the first four to six weeks of required training.

Responsibilities

  • Understand study protocols and complete required medical procedures.
  • Recruit study participants by calling the database, attending company-sponsored community events, and posting flyers in schools, senior centers, supermarkets, and other establishments.
  • Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs.
  • Conduct screening visits and study-protocol-specific participant visits, and assist staff physicians in assessing concomitant medications, adverse events, laboratory results, and other test results.
  • Prepare and monitor study supplies and stock levels in the clinic or hospital.
  • Ensure basic study participant safety.
  • Assist with monitor visits, including room setup.
  • Maintain and update knowledge of Clinical Operating Guidelines and apply them appropriately.
  • Assume an appropriate role with study participants and caregivers.
  • Ensure the quality and accuracy of source and CRF documentation.
  • Comply with Quality Management department guidelines and complete corrections for Quality Management, CRC, and Monitor/Sponsor Representative in a timely manner.

Desired Qualifications

  • CPT or phlebotomy experience is highly preferred.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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