Clinical Research Specialist I Position Available In Mecklenburg, North Carolina

Tallo's Job Summary: The Clinical Research Specialist I coordinates, collects, and processes clinical trial data under supervision, ensuring compliance and maintaining research protocol data. Requires a high school diploma, with preferred experience in clinical research or healthcare. Must have exceptional organizational skills, attention to detail, and be proficient in Microsoft Office. Valid driver's license required. Job Opening ID 83471.

Company:
Novant Health
Salary:
JobFull-timeOnsite

Job Description

Job Summary The Clinical Research Specialist I is responsible for the coordination, collection, processing and quality control of clinical trial data under the direct supervision of the Manager Clinical Research. Maintains all research protocol data and compliance reporting. Assists with screening of and consent from patients for research protocol regimens. Dedicated to excellence in all aspects of clinical research with a keen focus on ethics, safety, quality, compliance and stewardship. Come join a remarkable team where quality care meets quality service, in every dimension, every time. Let Novant Health be the destination for your professional growth. At Novant Health, one of our core values is diversity and inclusion. By engaging the strengths and talents of each team member, we ensure a strong organization capable of providing remarkable healthcare to our patients, families and communities. Therefore, we invite applicants from all group dynamics to apply to our exciting career opportunities. Responsibilities It is the responsibility of every Novant Health team member to deliver the most remarkable patient experience in every dimension, every time. + Our team members are part of an environment that fosters team work, team member engagement and community involvement. + The successful team member has a commitment to leveraging diversity and inclusion in support of quality care. + All Novant Health team members are responsible for fostering a safe patient environment driven by the principles of “First Do No Harm”. Qualifications +

Education:

High School Diploma or GED, preferred. 4 Year / Bachelors Degree, preferred. +

Experience:

Clinical Research or healthcare/medical experience preferred. Associate’s degree may substitute for 1 year of experience or Bachelor’s degree may substitute for 2 years of experience; Master’s degree may substitute for 3 years of experience. Certification (ACRP/SOCRA/equivalent) preferred. +

Licensure/Certification:

Valid driver’s license in appropriate state, required. + Additional Skills (required): Must have exceptional organizational and analytical skills. Attention to detail. Self-motivated and able to work independently. Able to meet multiple deadlines for concurrent projects. Work in a team- oriented setting. Must be proficient in Microsoft Office. Must provide own transportation to clinics, hospitals and associated agencies as required. Manual dexterity, prolonged standing or sitting. Able to lift light to medium weight objects which may be bulky and awkward. Ability to travel to developmental, educational and promotional activities. Physical and mental stamina required to function effectively in an environment with multiple fluctuating priorities. Ability to communicate effectively with individuals of all cultures and levels of authority. Exposure to hazardous materials (study agents, biohazards, pathology specimens). Job Opening ID 83471

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