Clinical Trial Assistant
50K–70K a year
Behavioral Health Market Context
Apply Nowvia JobLeads
Job Description
will assist with study documentation, trial tracking, vendor coordination, and regulatory submissions, ensuring compliance with GCP, SOPs, and applicable regulations.
Key Responsibilities
• Maintain and manage the Trial Master File (TMF) and study documentation.
• Support the preparation and coordination of clinical trial meetings and submissions.
• Track study progress, patient enrollment, and site communications.
• Liaise with internal teams, CROs, and site personnel to ensure efficient trial operations.
• Ensure timely and accurate data entry and document filing.
Qualifications
• Bachelor’s degree in life sciences or related field.
• 0–3 years of CTA experience in clinical research, preferably in rare disease or orphan indications.
• Strong organizational skills and attention to detail.
• Familiarity with GCP, ICH guidelines, and clinical trial processes.
If interested in this position, please reach out to [email protected].
Key Responsibilities
• Maintain and manage the Trial Master File (TMF) and study documentation.
• Support the preparation and coordination of clinical trial meetings and submissions.
• Track study progress, patient enrollment, and site communications.
• Liaise with internal teams, CROs, and site personnel to ensure efficient trial operations.
• Ensure timely and accurate data entry and document filing.
Qualifications
• Bachelor’s degree in life sciences or related field.
• 0–3 years of CTA experience in clinical research, preferably in rare disease or orphan indications.
• Strong organizational skills and attention to detail.
• Familiarity with GCP, ICH guidelines, and clinical trial processes.
If interested in this position, please reach out to [email protected].
Qualifications
- •Bachelor’s degree in life sciences or related field
- •0–3 years of CTA experience in clinical research, preferably in rare disease or orphan indications
- •Strong organizational skills and attention to detail
- •Familiarity with GCP, ICH guidelines, and clinical trial processes
Benefits
Responsibilities
- •They are seeking a detail-oriented Clinical Trial Assistant (CTA) to support the planning, execution, and oversight of clinical trials focused on rare diseases
- •The CTA will assist with study documentation, trial tracking, vendor coordination, and regulatory submissions, ensuring compliance with GCP, SOPs, and applicable regulations
- •Maintain and manage the Trial Master File (TMF) and study documentation
- •Support the preparation and coordination of clinical trial meetings and submissions
- •Track study progress, patient enrollment, and site communications
- •Liaise with internal teams, CROs, and site personnel to ensure efficient trial operations
- •Ensure timely and accurate data entry and document filing
More Jobs
- Remote Board Certified Behavior Analyst (BCBA)- Supporting ABA Centers in NCat Autism 360
- Clinical Trials Assistant Coordinator - Research Supportat Rehabilitation and Neurological Services, LLC
- Clinical Trials for Moneyat Care Health
- BCBA - Flexible, Impactful Autism Services (Remote/Hybrid)at Key Autism Services
- Hiring BCBA Roles at Team PBSat Positive Behavior Supports Corporation
- LMFT | Ankeny, Iowaat ProCare Therapy
- ID 6619 - Speech Language Pathologist - 1.0 FTE for 191 days/yearat Lake Oswego Public Schools
- Board Certified Behavior Analystsat Akoya Behavioral Health
- Atlantic Behavioral Excellenceat BK Behavior
- Hiring BCBA Roles at Team PBSat Positive Behavior Supports Corporation