Clinical Trial Associate

MacroGenics, Inc., a growing biotechnology company, has an opening for a Clinical Trial Associate in Rockville, MD. Responsibilities include processing study related documents to include routing for review/approval, collation and filing; create and maintain paper and/or electronic clinical study files; place documents in electronic document management system as directed; format documents for presentation; create and maintain tracking documents; schedule internal and external meetings as needed and maintain action logs; order study supplies and oversee inventory; prepare and send study related documents to CRO, Investigators, etc; initiate request for vendor payments; support day to day activities of clinical team as needed.

 

Applicants must meet the following requirements: Bachelor’s degree preferred; relevant experience considered (ie; minimum of 1 year experience supporting clinical trial teams or practical experience in an office environment); demonstrated proficiency with Microsoft Office, particularly Word, Outlook, Excel and PowerPoint; excellent interpersonal, communication, written and organizational skills; possess a sense of urgency in completing tasks without sacrificing accuracy; ability to work independently and on a team; ability to coordinate and prioritize multiple tasks; good organizational and problem solving skills.

 

Send resume and salary requirements to 1500 East Gude Drive, Rockville, MD 20850, email to HResources@macrogenics.com , or fax to (301) 251-5321. Reference Job Code #08018 in all correspondence.  Visit www.macrogenics.com for more details.

 

MacroGenics, Inc. is an Equal Opportunity Employer.