Clinical Research Associate for Rare Diseases or Oncology Trials (Des Moines)
If you are dedicated to advancing clinical research and have up to 2 years of experience as a Clinical Research Coordinator specifically in Rare Diseases or Oncology Clinical Trials, we are excited to connect with you!
Key Requirements:
• Experience with Rare Diseases or Oncology Studies is essential.
• Availability to start on April 6, 2026.
• Willingness to attend in-person training in Raleigh, NC during the week of May 4th, 2026, if hired.
The APEX CRA program at Parexel is your entry point into clinical research, providing comprehensive training and practical experience while working closely with seasoned CRAs and Clinical Operations Leads. This is an incredible opportunity for growth and professional development!
As an APEX CRA, you will engage in project support, perform CRA initiation tasks, and interact with clinical sites, all aimed at laying the foundation for a successful career in clinical research. Your role will include gaining hands-on experience with crucial clinical systems, including CTMS, EDC, Safety Information Systems, and TMF platforms, all supported by ongoing mentorship from experienced colleagues.
The responsibilities of a CRA at Parexel go beyond traditional monitoring tasks. You will cultivate strong relationships with clinical sites, support their success, and ensure high-quality management from site identification through to study close-out. Be prepared to conduct at least five site visits per month, with travel requirements of up to 80%.
Qualifications:
• Minimum Bachelor's degree in life sciences, data sciences, pharmacy, or a related health discipline.
• 6-24 months of clinical research experience.
• Exceptional interpersonal, written, and verbal communication skills.
• Ability to work independently and effectively manage urgent tasks with minimal oversight.
• A client-focused mindset and adaptability to learn new concepts.
• Proven capacity to juggle multiple priorities and navigate unpredictable scenarios while adhering to project timelines and study protocols.
• Commitment to ethical practices in developing innovative treatments.
• Strong computer skills with the eagerness to learn new systems.
• Essential experience in Rare Diseases or Oncology studies.
At Parexel, we take pride in being a global leader in clinical research. You will be part of a supportive culture that fosters personal connections and professional growth. Join a team that values knowledge sharing, encourages open communication, and provides excellent opportunities for career advancement.
Our competitive compensation for this role ranges from $60k to $70k, depending on factors like experience and location. Additional incentives and benefits, including paid time off, 401k match, health insurance, and more, are available for eligible employees.
#LI-REMOTE
Equal Opportunity Employer:
Parexel is proud to be an equal opportunity employer. All qualified applicants will be considered for employment regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Apply Now
Apply Now
Key Requirements:
• Experience with Rare Diseases or Oncology Studies is essential.
• Availability to start on April 6, 2026.
• Willingness to attend in-person training in Raleigh, NC during the week of May 4th, 2026, if hired.
The APEX CRA program at Parexel is your entry point into clinical research, providing comprehensive training and practical experience while working closely with seasoned CRAs and Clinical Operations Leads. This is an incredible opportunity for growth and professional development!
As an APEX CRA, you will engage in project support, perform CRA initiation tasks, and interact with clinical sites, all aimed at laying the foundation for a successful career in clinical research. Your role will include gaining hands-on experience with crucial clinical systems, including CTMS, EDC, Safety Information Systems, and TMF platforms, all supported by ongoing mentorship from experienced colleagues.
The responsibilities of a CRA at Parexel go beyond traditional monitoring tasks. You will cultivate strong relationships with clinical sites, support their success, and ensure high-quality management from site identification through to study close-out. Be prepared to conduct at least five site visits per month, with travel requirements of up to 80%.
Qualifications:
• Minimum Bachelor's degree in life sciences, data sciences, pharmacy, or a related health discipline.
• 6-24 months of clinical research experience.
• Exceptional interpersonal, written, and verbal communication skills.
• Ability to work independently and effectively manage urgent tasks with minimal oversight.
• A client-focused mindset and adaptability to learn new concepts.
• Proven capacity to juggle multiple priorities and navigate unpredictable scenarios while adhering to project timelines and study protocols.
• Commitment to ethical practices in developing innovative treatments.
• Strong computer skills with the eagerness to learn new systems.
• Essential experience in Rare Diseases or Oncology studies.
At Parexel, we take pride in being a global leader in clinical research. You will be part of a supportive culture that fosters personal connections and professional growth. Join a team that values knowledge sharing, encourages open communication, and provides excellent opportunities for career advancement.
Our competitive compensation for this role ranges from $60k to $70k, depending on factors like experience and location. Additional incentives and benefits, including paid time off, 401k match, health insurance, and more, are available for eligible employees.
#LI-REMOTE
Equal Opportunity Employer:
Parexel is proud to be an equal opportunity employer. All qualified applicants will be considered for employment regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Apply Now
Apply Now