So sorry, this position is no longer available.
Please go ahead and submit your application. We may have other positions that would be the perfect fit for you.
Alternatively, you may want to apply to one of the following related jobs:
Clinical Research Coordinator
Job Description
ONSITE 5 DAYS A WEEK / MUST BE US Citizen
Our client, a well-established dermatology practice known for clinical excellence, is hiring a Clinical Research Coordinator. This role offers an excellent opportunity to contribute to innovative dermatologic therapies within a collaborative, patient-focused environment. The successful candidate will coordinate and manage dermatology clinical trials, ensuring compliance with regulatory standards while supporting study participants and maintaining meticulous documentation.
Responsibilities:
- Screen, recruit, and enroll participants for dermatology clinical trials
- Conduct informed consent discussions with study participants
- Coordinate and perform study visits according to protocol requirements
- Maintain accurate source documentation and Case Report Forms (CRFs)
- Ensure compliance with FDA, GCP, and IRB regulations
- Manage investigational product accountability and study materials
- Document and report adverse events (AEs) and serious adverse events (SAEs)
- Maintain regulatory files including Trial Master Files (TMF)
- Assist physicians with dermatologic study procedures
- Obtain standardized pre- and post-treatment clinical photography
- Communicate effectively with sponsors, monitors, and internal research staff throughout the study
- Occasional travel for sponsor training may be required
Requirements:
- Prior experience as a Clinical Research Coordinator or research assistant; dermatology research experience strongly preferred
- Knowledge of Good Clinical Practice (GCP) and FDA regulations
- Understanding of clinical trial processes and medical terminology
- Familiarity with HIPAA and research compliance standards
- Strong organizational and documentation skills
- Ability to manage multiple studies and deadlines simultaneously
- Excellent interpersonal and communication skills
- Professional demeanor when interacting with patients, physicians, and sponsors
- Ability to work both independently and as part of a team
- CPR certification preferred
Some of the Benefits:
- Competitive salary
- Monday through Friday schedule with no weekends
- Opportunity to work in a respected dermatology practice with extensive clinical research experience
- Supportive and collaborative team environment
Salary: The posted range is not a guarantee. The actual salary will be based on qualifications, experience, and education and could fall outside of this range. Contact us for more information.
#LI-FP1
Meet Your Recruiter
Fran Philips
Vice President, Healthcare Recruitment
Fran is a seasoned recruiter who joined Tal in 2008, after a long career in medical billing for multi-specialty practices including dermatology, dental, and ophthalmology.
Learn more about Fran, Tal Healthcare Employee Biography
Share This Job:
Related Jobs:
Login to save this search and get notified of similar positions.
Clinical Research Coordinator
Job Description
ONSITE 5 DAYS A WEEK / MUST BE US Citizen
Our client, a well-established dermatology practice known for clinical excellence, is hiring a Clinical Research Coordinator. This role offers an excellent opportunity to contribute to innovative dermatologic therapies within a collaborative, patient-focused environment. The successful candidate will coordinate and manage dermatology clinical trials, ensuring compliance with regulatory standards while supporting study participants and maintaining meticulous documentation.
Responsibilities:
- Screen, recruit, and enroll participants for dermatology clinical trials
- Conduct informed consent discussions with study participants
- Coordinate and perform study visits according to protocol requirements
- Maintain accurate source documentation and Case Report Forms (CRFs)
- Ensure compliance with FDA, GCP, and IRB regulations
- Manage investigational product accountability and study materials
- Document and report adverse events (AEs) and serious adverse events (SAEs)
- Maintain regulatory files including Trial Master Files (TMF)
- Assist physicians with dermatologic study procedures
- Obtain standardized pre- and post-treatment clinical photography
- Communicate effectively with sponsors, monitors, and internal research staff throughout the study
- Occasional travel for sponsor training may be required
Requirements:
- Prior experience as a Clinical Research Coordinator or research assistant; dermatology research experience strongly preferred
- Knowledge of Good Clinical Practice (GCP) and FDA regulations
- Understanding of clinical trial processes and medical terminology
- Familiarity with HIPAA and research compliance standards
- Strong organizational and documentation skills
- Ability to manage multiple studies and deadlines simultaneously
- Excellent interpersonal and communication skills
- Professional demeanor when interacting with patients, physicians, and sponsors
- Ability to work both independently and as part of a team
- CPR certification preferred
Some of the Benefits:
- Competitive salary
- Monday through Friday schedule with no weekends
- Opportunity to work in a respected dermatology practice with extensive clinical research experience
- Supportive and collaborative team environment
Salary: The posted range is not a guarantee. The actual salary will be based on qualifications, experience, and education and could fall outside of this range. Contact us for more information.
#LI-FP1
Meet Your Recruiter
Fran Philips
Vice President, Healthcare Recruitment
Fran is a seasoned recruiter who joined Tal in 2008, after a long career in medical billing for multi-specialty practices including dermatology, dental, and ophthalmology.
Learn more about Fran, Tal Healthcare Employee Biography