Clinical Trial Associate
3 months ago
The Clinical Trial Associate supports our Clinical Operations team(s) and the Clinical Trial Manager(s) in the overall management of trials, including planning, execution, and closeout of one or more clinical trials in a fast-paced environment.
- Length of Assignment– 6 months to start (extension potential based on performance/business needs).
- Hours: Full-time, 40 hours per week
- Fully remote – must work EST hours.
- CRO, sponsor, or industry experience preferred.
Key Responsibilities
- Scheduling activities and meetings, including compilation of materials and overseeing presentations.
- Responsible for taking and distributing meeting minutes for both internal and external meetings as well as reviewing for accuracy.
- Review and submit files within the Trial Master File, for Clinical Operations-related documentation.
- Filing and routing of agreements related to Clinical Operations
- Creating, distributing, and updating trackers for metric reporting
- Supports the Clinical Trial Manager(s) on one or more clinical trials.
- Assists with preparation of reports and/or requests as required.
- Support departmental initiatives and process improvements.
- Minimal travel required (10% both international and domestic)
- Other duties and responsibilities as required
Key Skills, Abilities, and Competencies
- Ability to organize and manage multiple priorities and/or projects.
- Ability to manage time, plan, and organize effectively.
- Strong written and verbal communication skills
- Attention to detail and thorough follow-up skills.
- Participate in coordination of clinical trial related activities.
- Demonstrated computer skills (Microsoft Suite)
- Maintenance and management of study/program trackers
- Knowledge of ICH/GCP/local regulations
- Effectively and efficiently interact with internal and external personnel
Requirements
- Education, Registration &/Or Certifications: B.S/B.A. degree is required. Science/health care related field preferred but not required.
- Experience: Minimum 1 year of professional experience or equivalent. Prior experience in the biotech, pharmaceutical, or medical device industry is preferred. Prior experience with systems (e.g., eTMF, IRT, EDC) preferred.
Company DescriptionBeacon Hill is an Equal Opportunity Employer that values the strength diversity brings to the workplace. Individuals with Disabilities and Protected Veterans are encouraged to apply.
If you would like to complete our voluntary self-identification form, please click here or copy and paste the following link into an open window in your browser: https://jobs.beaconhillstaffing.com/eeoc/
Completion of this form is voluntary and will not affect your opportunity for employment, or the terms or conditions of your employment. This form will be used for reporting purposes only and will be kept separate from all other records.Company DescriptionBeacon Hill is an Equal Opportunity Employer that values the strength diversity brings to the workplace. Individuals with Disabilities and Protected Veterans are encouraged to apply.\r
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If you would like to complete our voluntary self-identification form, please click here or copy and paste the following link into an open window in your browser: https://jobs.beaconhillstaffing.com/eeoc/\r
\r
Completion of this form is voluntary and will not affect your opportunity for employment, or the terms or conditions of your employment. This form will be used for reporting purposes only and will be kept separate from all other records.
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