Clinical Research Associate, Sponsor Dedicated

IQVIA; Afton (WY); On-site; USD 71,900 - 189,000; Full time

Job summary

IQVIA is hiring for a position focused on monitoring and site management to ensure compliance with study protocols in Afton, Wyoming. Ideal candidates have at least two years of on-site monitoring experience and a Bachelor’s in a scientific discipline or healthcare. You will work closely with sites, ensuring adherence to Good Clinical Practice and relevant regulations.

The compensation range varies from $71,900 to $189,000 annually, depending on experience and other factors. This role comes with a comprehensive benefits package.

Qualifications

• Minimum 2 years of on-site monitoring experience.
• Knowledge of Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.
• Proficient computer skills and familiarity with devices like iPhone and iPad.

Responsibilities

• Perform site monitoring visits and ensure compliance with study protocols.
• Work with sites to enhance subject recruitment plans.
• Evaluate site practices and ensure quality and integrity of study conduct.

Skills

On-site monitoring experience

Good knowledge of clinical research regulations

Effective communication skills

Organizational skills

Time management skills

Education

Bachelor's Degree in a scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

To be eligible for this position, you must reside in the same country where the job is located.

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

• Perform site monitoring visits (selection, initiation, monitoring and close‑out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start‑up phase.
• Ensure copies/originals (as required) of site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow‑up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

• Bachelor's Degree in a scientific discipline or health care preferred.
• Requires at least 2 years of on‑site monitoring experience.
• Equivalent combination of education, training and experience may be accepted in lieu of a degree.
• Good knowledge of and skill in applying applicable clinical research regulatory requirements.
• Good clinical practice (GCP) and International Conference on Harmonisation (ICH) guidelines.
• Good therapeutic and protocol knowledge as provided in company training.
• Computer skills including proficiency in Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad where applicable.
• Written and verbal communication skills including good command of English language.
• Organizational and problem‑solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Benefits

The potential base pay range for this role, when annualized, is $71,900.00 - $189,000.00. The actual base pay offered may vary based on a number of factors including job‑related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part‑time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA is proud to be 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, status as a protected veteran, or any other status protected by applicable law.

IQVIA is committed to integrity in our hiring process and maintains a zero‑tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.