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Clinical Research Associate (Cra Ii/Senior)

1-2 years
Not Disclosed
10 Sept. 17, 2024
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

About This Role: Clinical Research Associate at Parexel

Working with Heart

At Parexel, we deeply understand that at the heart of every clinical trial, we are all patients. This empathy drives our approach, ensuring we deliver with care and dedication. Our clinical operating model prioritizes effectiveness by reducing handoffs and boosting satisfaction for employees, clients, and sites alike. As a Clinical Research Associate (CRA) with Parexel, you’ll be part of a team that combines diverse experiences and expertise to achieve exceptional outcomes. We seek proactive individuals who aim to improve processes, think innovatively, and grow both personally and professionally.

Your Role

As a CRA at Parexel, you’ll go beyond traditional monitoring roles. You’ll be the primary point of contact for clinical sites, managing relationships and ensuring their success throughout the study lifecycle. This role involves:

  • Conducting Visits: Perform site qualification (QV), initiation (SIV), monitoring (MV), and termination (TV) visits, and generate detailed reports.
  • Building Relationships: Foster strong rapport with site staff, ensuring the integrity of the study and addressing site issues effectively.
  • Protecting Patients: Safeguard the rights and well-being of participants, ensuring adherence to protocols.
  • Driving Productivity: Collaborate with sites to develop patient recruitment strategies, ensuring compliance with SOPs, protocols, GCP, and regulatory requirements.
  • Ensuring Quality: Monitor and evaluate data integrity, site performance, and drug accountability.
  • Executing Tasks: Oversee regulatory documentation, ensuring completeness and accuracy.

A Little About Us

At Parexel, we pride ourselves on being a leading global Clinical Research Organization. We foster a collaborative environment where team members build personal connections and share expertise. Our open discussions and support for career growth—whether in senior CRA roles, line management, quality, project leadership, or other areas—reflect our commitment to your professional development.

What We Expect From You

  • Experience: Minimum of 18 months as a CRA with experience in clinical research, including oncology monitoring.
  • Education: Bachelor’s degree or equivalent in biological sciences, pharmacy, or a related health discipline.
  • Skills: Strong interpersonal, written, and verbal communication skills, with a self-driven approach and minimal need for oversight.
  • Attributes: A client-focused attitude, flexibility in handling assignments, and the ability to manage multiple tasks and meet project timelines.
  • Technical Skills: Proficiency in Clinical Trial Management Systems (CTMS), Electronic Document Management Systems (EDMS), and MS Office (Excel, Word).

Additional Information

  • Remote Work: This position is remote.
  • EEO Disclaimer: Parexel is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

If you are looking for a role where you can make a meaningful impact, grow your career, and work in a supportive environment, Parexel might be your perfect fit. Join us in advancing clinical research and improving patient outcomes.