Assistant Clinical Project Manager

Assistant Clinical Project Manager Beaufort LLC Virginia Beach, VA Job Details Full-time 1 day ago Qualifications Project reporting Clinical research Writing skills Filing Data reporting Research Mid-level ICH guidelines Bachelor's degree Research compliance clinical trial records management Productivity software Data collection Healthcare data collection Microsoft Project Communication skills Project scheduling Full Job Description 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.