Beaufort is seeking an Assistant Clinical Project Manager (APM) to join our growing Clinical Operations team. In this role, the APM will serve as a primary point of contact for investigative sites and Beaufort Clinical Project Managers, providing essential operational support across assigned studies. This position offers a unique opportunity to gain hands-on experience within a CRO environment while collaborating with multiple Sponsors across diverse therapeutic areas and indications in a fast-paced, innovative industry.
Responsibilities:
- Plan, implement, and oversee specific tasks and functions within a clinical research engagement under the guidance of a Clinical Project Manager.
- Collect project related data and information across multiple studies.
- Prepare activity reports for internal and external distribution.
- Assist with creation and tracking of project timeline and activities
- Maintain both electronic and physical Trial Master Files.
- Maintain study systems and project trackers to track and record study data.
- Provide support to PM and CRAs with site management and study logistics, including documents collection, sample management, site contracting support.
- Assist Project Managers in addressing and resolving study issues and completing other tasks as assigned.
- Assist with site feasibility conduct.
- Collect and maintain study metrics (clinical metrics, financial, timeline), analyze data, and produce reports
Qualifications:
- Bachelor's Degree required.
- Previous Clinical Research experience- Site, CRO, or Sponsor level, is REQUIRED.
- Experience with Clinical Trial Systems – EDC, CTMS, eTMF
- Strong experience with MS Office – specifically MS Project, Excel, Power Point and Word
- PMP Certification (it is a plus)
- Must have excellent oral and written communication skills.
- Must have the ability to be flexible and change priorities quickly.
- Must be able to strictly follow ICH/GCP guidelines, SOPs, and meet all deadlines.
Why Join Beaufort?
Beaufort offers a different CRO experience. It’s not just about what we do, it’s how we do it. Together our team brings a level of passion knowledge and commitment to our projects and clients. We foster a culture of excellence clinical project management and regulatory support.
At Beaufort you will be part of industry leading expertise with a shared sense of purpose and unwavering accountability to help clients achieve successful market authorization.
Beaufort is an equal opportunity employer and values diversity. We offer a highly competitive compensation and benefits package.