Clinical Research Coordinator Level 2 - Winston-Salem, NC
Winston-Salem, NCFull-time
22.25–29.75 an hour
Behavioral Health Market Context
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Benefits
Health Insurance
Job Description
various domains including pharmaceuticals, biotechnology, and medical devices, helping to bring new and effective therapies to patients worldwide. The company is known for its collaborative culture, comprehensive training programs, and strong emphasis on employee growth and development. ICON welcomes applicants from diverse backgrounds and prioritizes a work environment free from discrimination and harassment, ensuring equal opportunities for all qualified individuals. The company supports flexibility, work-life balance, and well-being through its extensive benefits package focused on personal and professional sustainability.
The Clinical Research Coordinator 2 (CRC Level 2) position at ICON's Accellacare team in Winston-Salem, North Carolina, offers an exciting opportunity for professionals passionate about clinical research and patient care. The role is onsite, located at 1901 S. Hawthorne Road, Suite 306, Winston-Salem, NC. In this role, you will be instrumental in ensuring volunteer safety, promoting the mission of Accellacare, and meeting or exceeding study priorities. The CRC 2 is responsible for recruiting eligible participants and engaging with sponsor representatives to advance clinical trials. This position demands a detail-oriented, motivated individual with at least one year of clinical research or pharmaceutical experience, preferably with a background in neurology or psychiatric clinical trials. The CRC will manage various study-related tasks, including performing clinical procedures such as venipuncture, ECGs, IV infusions, and allergy testing, among others. Attending investigator meetings and site initiation visits ensures continuous learning and adherence to protocol standards.
The role involves meticulous documentation, management of study drugs and clinical supplies, temperature monitoring for specimen integrity, and regulatory compliance preparing for audits. Acting as the OSHA Representative, the CRC also oversees safety protocols such as immunization records and vaccination administration for site staff. ICON's Accellacare clinical research network aims to transform the clinical trial experience by enhancing access, efficiency, and outcomes for both patients and sponsors. The role supports a collaborative team environment where you can grow your clinical skills and contribute meaningfully to advancing health science. ICON offers competitive compensation along with a comprehensive benefits package designed to support your well-being and professional journey.
• Bachelor's degree in life sciences or related field
• Minimum one year experience in clinical research or pharmaceutical environment
• Prior experience as Clinical Research Coordinator
• Knowledge of clinical procedures and study protocol requirements
• Ability to perform technical tasks such as venipuncture and IV infusions
• Strong organizational and documentation skills
• Effective communication skills
• Commitment to patient safety and protocol compliance
OysterLink supports hiring across hospitality industries.
The Clinical Research Coordinator 2 (CRC Level 2) position at ICON's Accellacare team in Winston-Salem, North Carolina, offers an exciting opportunity for professionals passionate about clinical research and patient care. The role is onsite, located at 1901 S. Hawthorne Road, Suite 306, Winston-Salem, NC. In this role, you will be instrumental in ensuring volunteer safety, promoting the mission of Accellacare, and meeting or exceeding study priorities. The CRC 2 is responsible for recruiting eligible participants and engaging with sponsor representatives to advance clinical trials. This position demands a detail-oriented, motivated individual with at least one year of clinical research or pharmaceutical experience, preferably with a background in neurology or psychiatric clinical trials. The CRC will manage various study-related tasks, including performing clinical procedures such as venipuncture, ECGs, IV infusions, and allergy testing, among others. Attending investigator meetings and site initiation visits ensures continuous learning and adherence to protocol standards.
The role involves meticulous documentation, management of study drugs and clinical supplies, temperature monitoring for specimen integrity, and regulatory compliance preparing for audits. Acting as the OSHA Representative, the CRC also oversees safety protocols such as immunization records and vaccination administration for site staff. ICON's Accellacare clinical research network aims to transform the clinical trial experience by enhancing access, efficiency, and outcomes for both patients and sponsors. The role supports a collaborative team environment where you can grow your clinical skills and contribute meaningfully to advancing health science. ICON offers competitive compensation along with a comprehensive benefits package designed to support your well-being and professional journey.
• Bachelor's degree in life sciences or related field
• Minimum one year experience in clinical research or pharmaceutical environment
• Prior experience as Clinical Research Coordinator
• Knowledge of clinical procedures and study protocol requirements
• Ability to perform technical tasks such as venipuncture and IV infusions
• Strong organizational and documentation skills
• Effective communication skills
• Commitment to patient safety and protocol compliance
OysterLink supports hiring across hospitality industries.
Qualifications
- •This position demands a detail-oriented, motivated individual with at least one year of clinical research or pharmaceutical experience, preferably with a background in neurology or psychiatric clinical trials
- •Minimum one year experience in clinical research or pharmaceutical environment
- •Prior experience as Clinical Research Coordinator
- •Knowledge of clinical procedures and study protocol requirements
- •Ability to perform technical tasks such as venipuncture and IV infusions
- •Strong organizational and documentation skills
- •Effective communication skills
- •Commitment to patient safety and protocol compliance
Benefits
- •The company supports flexibility, work-life balance, and well-being through its extensive benefits package focused on personal and professional sustainability
- •The role supports a collaborative team environment where you can grow your clinical skills and contribute meaningfully to advancing health science
- •ICON offers competitive compensation along with a comprehensive benefits package designed to support your well-being and professional journey
- •Bachelor's degree in life sciences or related field
Responsibilities
- •In this role, you will be instrumental in ensuring volunteer safety, promoting the mission of Accellacare, and meeting or exceeding study priorities
- •The CRC 2 is responsible for recruiting eligible participants and engaging with sponsor representatives to advance clinical trials
- •The CRC will manage various study-related tasks, including performing clinical procedures such as venipuncture, ECGs, IV infusions, and allergy testing, among others
- •Attending investigator meetings and site initiation visits ensures continuous learning and adherence to protocol standards
- •The role involves meticulous documentation, management of study drugs and clinical supplies, temperature monitoring for specimen integrity, and regulatory compliance preparing for audits
- •Acting as the OSHA Representative, the CRC also oversees safety protocols such as immunization records and vaccination administration for site staff
- •ICON's Accellacare clinical research network aims to transform the clinical trial experience by enhancing access, efficiency, and outcomes for both patients and sponsors
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