FREELANCE Clinical Research Associate

SanaClis; California (MO); On-site; USD 41,328 - 61,992; Part time

Benefits offered by this job

Great work-life balance

Career growth opportunities

Friendly work environment

Job summary

A global clinical research organization is seeking a part-time Freelance Clinical Research Associate (CRA) to join their team. The role involves monitoring clinical trials, ensuring compliance with regulations, and maintaining data integrity. The ideal candidate should have a Bachelor’s degree in life sciences or related fields, with at least 2 years of relevant experience. English proficiency at C1 level is required, and a valid driving license with travel capability is essential. Enjoy a balanced work-life environment and growth opportunities.

Qualifications

• Minimum 2 years of experience of onsite monitoring activities.
• Driving license B and ability to travel.
• Profound knowledge of medical terminology.

Responsibilities

• Monitor clinical trials and ensure compliance with regulations.
• Guarantee data quality and integrity meeting clinical standards.
• Develop collaborative relationships with investigational sites.

Skills

Monitoring clinical trials

Knowledge of ICH GCP

Clinical research processes

Fluent English (C1)

Education

Bachelor’s degree in life sciences or medical sciences

Job description

We are looking for a FREELANCE, PART-TIME CRA to strengthen our clinical operations team in Ventura, Illinois & Ohio!

Job Requirements

• Bachelor’s degree required – preferred qualification in life sciences or medical sciences
• Minimum 2 years of experience of onsite monitoring activities
• Profound knowledge of clinical research processes and medical terminology
• Expert knowledge of ICH GCP, and international and local regulatory requirements
• Passion for clinical research
• English language proficiency of minimum level C1 (ref. CEFR) – fluent in written and spoken English
• Driving license B and ability to travel

Job Responsibilities

• You would be primarily responsible for monitoring clinical trials and
• Ensuring that clinical trial is conducted, recorded, and reported in accordance with all applicable international and local regulations and guidelines, good practices, SOPs and Clinical Trial Protocol
• Ensuring data quality and integrity meet acceptable clinical standards
• Guaranteeing the rights and safety of patients involved in a study are protected
• Performing and coordinating all aspects of the clinical monitoring and site management process
• Conducting remote and on-site visits to assess protocol and regulatory compliance and managing required documentation
• Developing collaborative relationships with investigational sites, act as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects rights, well-being, and data reliability; and you would ensure audit readiness.
• Serving as facilitator of Clinical Trial conduct in respective area in terms of identifying qualified sites and investigators, facilitating communication between sponsor and regulatory authorities and trial sites.

What We Offer

• Great work-life balance (You will not be overwhelmed with projects as we believe in quality over quantity)
• Career growth and development opportunities in a continuous learning culture
• Friendly environment in a privately owned international company
• Additional benefits will be discussed during the interview

You can apply via the link or send a CV directly to: [e-mail]

* SanaClis is an equal employment opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin, ancestry, age, disability, marital status, pregnancy, protected veteran status, order of protection status, protected genetic information, or any other characteristic protected by law.