Clinical Research Coordinator

Description:

Working at a top-ranked research company, the Clinical Research Coordinator works under the general direction of the Principal Investigator to ensure protocols are conducted in accordance with the principles of Good Clinical Practice. The coordinator will coordinate clinical research studies and perform a variety of duties involved in the collection, compilation, and documentation of clinical research data. The coordinator will play a key role in coordinating all clinical trial activities, by following all applicable regulations governing the conduct of clinical trials. The primary skills include GCP proficiency, logical thinking, ability to prioritize, a can-do attitude, the ability to adapt quickly to changing business conditions, and strong interpersonal, and team-building skills.

The coordinator, working closely with study team members under the moderate direction of a Study Investigator, will have overall responsibilities for coordinating efforts with other study team members in order to achieve study objectives and corporate goals, including:

Coordinate the day to day activities of the research visits by completing all assessments required for the visit (eg Vital signs, EKG, labwork).

The Clinical Research Coordinator will ensure that subjects participating in a clinical trial are following the study protocol as directed.

Maintain study source documents. Report adverse events.

Educate subjects on protocol, study intervention, study drugs, etc.

Ensures the data collected is accurate, legible, organized by follow good clinical practices. .

Skills:

Chart review, Clinical research, Clinical trial, Patient recruitment

Top Skills Details:

Chart review,Clinical research,Clinical trial,Patient recruitment

Additional Skills & Qualifications:

Requires a minimum of 2 yrs of experience in healthcare.

Strong interpersonal skills with attention to detail are a must. Demonstrated ability in positive relationship building, with strong verbal and written skills required.

Ability to travel for Clinic activities, attend investigator meetings, or vendor visits/audits, as required.

Familiar with the background of the study drug and requirements of the study

Must demonstrate a passion for direct patient interaction

Demonstrate clinical competence, positive leadership, and ability to work collaboratively with a multi-disciplinary team

Prolonged periods of sitting at a desk and working on a computer

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.