Clinical Research Associate
4 weeks ago
Job Title: FSP-SCRA I
Job Summary:
Fortrea is seeking a Clinical Research Associate I to support the execution of clinical trials across multiple therapeutic areas. The successful candidate will be responsible for conducting site visits, managing study documentation, and ensuring compliance with regulatory requirements.
Essential Responsibilities:
- Conduct site visits to ensure compliance with Good Clinical Practice (GCP) and regulatory requirements
- Manage study documentation, including case report forms and informed consent forms
- Collaborate with site staff to ensure timely completion of study milestones
- Identify and escalate any issues or concerns related to study conduct or compliance
- Participate in study initiation, monitoring, and close-out activities
- Develop and maintain relationships with site staff and investigators
- Provide support to study teams as needed
- Perform other duties as assigned by management
Requirements:
- 2+ years of experience in clinical research, preferably as a Clinical Research Associate
- Strong knowledge of GCP, regulatory requirements, and clinical trial protocols
- Excellent communication and interpersonal skills
- Ability to work independently and as part of a team
- Strong organizational and time management skills
- Proficiency in Microsoft Office and clinical trial management systems
Preferred Qualifications:
- Bachelor's degree in a life science or related field
- Experience with electronic data capture systems
- Knowledge of ICH/GCP and regulatory requirements
- Fluency in multiple languages
About Fortrea:
Fortrea is a global contract research organization (CRO) that provides pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.
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