Intern- Clinical Trial Management

Position Summary

The Clinical Trial Management Intern will support our Clinical Trial Management team in the overall foundational organization of our clinical trials, including planning, execution, and closeout with the goal of increasing efficiency and consistency within the function.

The intern will report to a member of the Clinical Trial Management team and will be based on-site in RTP, NC.

Job Responsibilities

• Schedule activities and meetings, including compilation of materials and overseeing presentations
• Responsible for taking and distributing meeting minutes and tracking action items for both internal and external meetings as well as reviewing for accuracy
• Participate in clinical trial management study-related activities on an as needed basis
• Assist the CTMs in tracking various components of the clinical studies
• Take meeting minutes and track actions as applicable for clinical trial activities
• Review and submit files within the Trial Master File, for Clinical Operations-related documentation
• Track review of and file monitoring reports and associated documents
• Collaborate with cross-functional team members during normal business operations
• Creating, distributing, and updating trackers for metric reporting
• Support departmental initiatives and process improvements
• Other duties and responsibilities as required

Minimum Requirements

• Must be pursuing a Bachelor’s degree in a scientific, healthcare, project management or related field
• Must be at least a Junior in university at the time of your application
• Proficient computer skills (Microsoft Suite, SmartSheet) and ability to learn new technologies quickly
• Excellent verbal and written communication skills
• Proactive and solution-driven mindset
• Strong sense of accountability and ability to prioritize multiple tasks
• Excellent organizational skills and attention to detail
• Flexible and willing to support a variety of tasks for the Clinical Trial Management team
• Available to work full-time during the summer months (May-August) at an AskBio office

Preferred Education, Experience and Skills

• Students enrolled in a Master’s program in a scientific, healthcare or project management related field are encouraged to apply
• Prior internship, work, or volunteer/extracurricular experience

AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid job‐related requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at (919) 561-6210 or sending us an email at careers@askbio.com.

Agencies:  Please do not contact any employee at AskBio about this requisition.  Any resume submitted by a recruitment agency to any employee at AskBio, through any medium, will be deemed the sole property of AskBio unless the agency was engaged by AskBio Talent Acquisition team to recruit for that position.  All agencies must have a prior executed service agreement with AskBio prior to any search engagement.  If a candidate who was submitted outside of the AskBio agency process is hired by AskBio, no fee or payment of any kind will be paid to the agency.