Clinical Research Associate, Sponsor Dedicated

IQVIA Argentina; Marysville (WA); On-site; USD 71,900 - 189,000; Full time

Job summary

IQVIA Argentina is seeking a Clinical Research Associate in Marysville, United States to conduct site monitoring visits and ensure compliance with clinical trial protocols. The ideal candidate will have a Bachelor’s degree and at least 2 years of relevant experience.

Responsibilities include managing study progress, evaluating site practices, and collaborating with the study team. The expected annual salary ranges from $71,900 to $189,000 depending on experience and qualifications.

Qualifications

• Minimum of 2 years of on-site monitoring experience.
• Good knowledge of clinical research regulatory requirements like GCP.
• Proficient in using computer skills, particularly Microsoft Office.

Responsibilities

• Perform site monitoring visits in accordance with contracted scope of work.
• Evaluate site practices related to protocol conduct and adherence.
• Manage progress of assigned studies through various tracking methods.

Skills

On-site monitoring experience

Clinical research regulatory knowledge

Communication skills

Organizational skills

Problem-solving skills

Education

Bachelor's Degree in a scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Laptop, iPhone, iPad

Job description

Clinical Research Associate, Sponsor Dedicated

Marysville, United States of America | Full time | Field-based | R1541733

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

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) 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 (e.g., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
• Good therapeutic and protocol knowledge as provided in company training.
• Computer skills including proficiency in use of 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.

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.