Clinical Research Associate II

Premier Research; España; Hybrid; PHP 3,762,000 - 5,643,000; Full time

Job summary

Premier Research is seeking a Clinical Research Associate II to join our Clinical Monitoring, Site Management and SSU team. The role supports biotech, medtech, and specialty pharma partners to advance medicines and diagnostics, with growth opportunities and flexible work options.

You will monitor trials across sites with focus on patient safety and data integrity, prepare monitoring visits, and maintain essential trial documents in line with ICH/GCP.

Qualifications

• 2+ years of experience in clinical trials and independent monitoring.
• Experience in Neurology, Oncology, Rare Diseases & Pediatrics is beneficial.
• Willingness to monitor country-wide; capable of remote, hybrid, or onsite work.

Responsibilities

• Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines.
• Maintains submission of expenses according to travel and expense requirements within company guidelines.
• Monitors (remote, onsite, or other approved mode of monitoring) with a focus on data integrity and patient safety in accordance with country regulations.
• Plans day to day activities for monitoring of a clinical study and sets priorities per site.
• Prepares for and conducts on-site qualification, study initiation, interim monitoring, and close-out monitoring visits at investigator sites as required by clinical monitoring plan.
• Maintains Trial Master File (TMF)/electronic Trial Master File (eTMF) per guidelines; understands essential documents per ICH/GCP Section 8.
• Reviews site documents and verifies they are accurate, complete, current, and include required updates.

Skills

Clinical monitoring

Data integrity

Patient safety

Study planning

TMF/eTMF familiarity

Education

Undergraduate degree in clinical/science/health

Licensed health-care professional (RN)

Job description

Premier Research is looking for a Clinical Research Associate II to join our Clinical Monitoring, Site Management and SSU team.

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.

Your ideas influence the way we work, and your voice matters here.

As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.

Job Description

What You'll be Doing:

• Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines
• Maintains submission of expenses according to travel and expense requirements within company guidelines
• Monitors (remote, onsite, or other approved mode of monitoring) with a focus on data integrity and patient safety in accordance with specific country regulations
• Plans day to day activities for monitoring of a clinical study and sets priorities per site
• Prepares for and conducts on-site qualification, study initiation, interim monitoring, and close-out monitoring visits at investigator sites as required by clinical monitoring plan
• Maintains Trial Master File (TMF)/electronic Trial Master File (eTMF) as defined by the organization’s processes per filing guidelines. Understands the required essential documents according to ICH/GCP Section 8.
• Reviews site documents and verifies they are accurate, complete, current, and include required updates

What We Are Searching For

• Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required
• Previous clinical research experience required
• At least 2+ years’ experience in clinical trials and independent monitoring
• Experience working in one or more of the following therapy areas will be beneficial; Neurology, Oncology, Rare Diseases & Pediatrics
• Preference at working across all phases I-IV, although phase II and III only will be considered

The role can be offered as fully remote, hybrid or office based. There will be an expectation for country-wide monitoring with the average frequency of days on site being 6 days per month.