Clinical Research Specialist – Novant health jobs in New York

novant health jobs in New York

Job highlights

Identified by Google from the original job post

Qualifications

• 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
• 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)

Responsibilities

• 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 the 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
• 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 teamwork, 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”

Job description

Overview

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 the 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.

This is an entry-level role in Clinical Research. Must be located in the Winston-Salem, NC area.

Come join a remarkable team where quality care meets quality service, in every dimension, every time.

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.

Qualifications
• Education: High School Diploma or GED, preferred. 4 Year / Bachelor’s 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).

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 teamwork, 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”.

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