(Clinical) Research Assistant

This Clinical Research position is an ON - SITE part time role in Thousand Oaks-- Los Angeles, California area; this will be a hourly support position with approximately 24 hours a week.

Description:

This role will perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.

The Research Assistant (RA) position delivers a strong customer experience for both sites and patients by providing virtual study support under the delegation of a PI. The RA is accountable for study delivery at the patient level and is expected to support the patient experience, data management, and other study administrative tasks with a quality-first approach. This is an early-to-mid experience position with the expectation that the RA has working knowledge of and experience in the clinical research industry. This position is an onsite part time, hourly role with approximately 24 hours a week.

Additional Skills & Qualifications:

· Data extraction from source documents and assist CRC with query resolution

· Basic knowledge of clinical trials and medical terminology

· In-depth understanding of departmental, protocol, and study-specific procedures

· Proficiency in MS Windows and Office applications (Access, Outlook, Excel, Word)

· Excellent interpersonal and communication skills

· Strong attention to detail and ability to work independently.

· Adaptability to a fast-paced environment

· Familiarity with medical and research terminology

· Knowledge of federal regulations and Good Clinical Practices (GCP)

· Critical thinking and problem-solving abilities

· Customer-centric personality with a positive attitude under pressure

· Contribution to team and site goals

· High level of self-motivation and energy

· Optimistic "can-do" attitude

· Willingness to work onsite in Thousand Oaks-- Los Angeles, California.

Skills:

Clinical research, Clinical trial, Pre-screening patients, EDC

Top Skills Details:

Clinical Research, Clinical Trial

Certifications/Licenses, Education, and Experience:

· A minimum of 1-2 years clinical research experience.

· Research experience required.

Experience Level:

Intermediate Level

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.