Senior Clinical Research Associate

Advanced Clinical; Orlando (FL); Remote; USD 60,000 - 95,000; Full time

Job summary

An established industry player is seeking a dedicated Clinical Monitor to ensure compliance in clinical trials across various sites. This role offers the chance to work remotely while managing relationships with investigators and ensuring the safety and confidentiality of study subjects. With a focus on quality and reliability, you will conduct site visits and monitor data integrity, contributing significantly to the success of clinical research. The company values innovation and resilience, providing a supportive environment and competitive benefits to enhance your career in clinical development.

Benefits

Comprehensive medical, vision, and dental benefits

Unlimited PTO

Charity volunteer PTO

Wellness reimbursement

Tuition reimbursement

Visibility and recognition by leadership

Mentorship opportunities

Qualifications

• 3+ years of clinical monitoring experience required.
• Bachelor's degree preferred; RN may also be considered.

Responsibilities

• Ensure clinical trials comply with protocols and regulatory requirements.
• Conduct site qualification, initiation, and monitoring visits.

Skills

Clinical Monitoring

Regulatory Compliance

Data Quality Verification

Site Management

Education

Bachelor's Degree

Registered Nurse (RN)

Job description

***This position can work remotely anywhere in the United States***

What's in it for YOU?

• Competitive compensation with comprehensive medical, vision, and dental benefits package


• Unlimited PTO package with additional sick days


• 8 hours of additional PTO to volunteer for a charity of your choice and up to $120 paid to your charity for your commitment


• Wellness reimbursement up to $50 per month for fitness and wellness memberships


• Tuition reimbursement up to $5,000 per year


• Visibility and recognition by Senior leadership for positive contributions to the business


• Opportunity to have a voice and be a part of a very close-knit team (advice, reliability, mentorship, partnership)


• And more!

Responsibilities:

• Ensure clinical trials are conducted in compliance with protocol/amendment(s), with ICH GCP, SOPs and with applicable regulatory requirements in the assigned countries and sites


• Ensure subject safety and verify diligence in protecting the confidentiality and wellbeing of study subjects


• Verify adequacy, completeness, reliability, and quality of trial data collected at study sites


• Conduct site qualification, site initiation, interim monitoring and close out visits


• Develop and maintain site and investigator relationships to ensure clinical trials are managed efficiently

Qualifications:

• Bachelor's degree preferred; a Registered Nurse (RN) may also be considered


• 3+ years of clinical monitoring experience


• The ability to perform travel up to an average of 80%, depending on project needs


• This role may be office and/or home-based/field-based however regular infrequent visits to a Company office will also be required.


• Current passport or identity card with a valid driving license required

Advanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey. Our goal is to improve the lives of all those touched by clinical research - approaching each opportunity with foresight, character, resilience and innovation. Based on decades of experience, we help our clients achieve better outcomes by conducting candid conversations and anticipating potential issues through our customized solutions.