Research Associate
Research Associate
Posted on :
17-04-2025
Employer Active
1 Vacancy
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Share
Send me jobs like this
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Job Description
Job Description Summary
The Biostatistics Center of the Milken Institute School of Public Health is an offcampus research facility of The George Washington University located in Rockville Maryland. The Biostatistics Center serves as the coordinating center for large scale multicenter clinical trials and epidemiological studies funded by federal agencies including the National Institutes of Health. The Biostatistics Center is a leader in the statistical coordination of major medical research programs of national and international scope. Visit our website at: . The Biostatistics Center is seeking a fulltime Research Associate to work as a project manager of the data coordinating center team supporting the NIH funded MaternalFetal Medicine Units Network. Multiple clinical trials evaluating interventions to reduce adverse maternal and neonatal outcomes will be implemented in the next few years. The Research Associate will be responsible for providing study project management throughout phases of a clinical study including implementation conduct closeout and reporting. This position compiles results and prepares technical reports and documentation of outcomes. This role is familiar with standard concepts practices and procedures within a particular field. Working under general supervision this position typically reports to a Principal Investigator. Essential duties include: Maintains daily oversight of study activities and tasks list ensuring timely completion. Collaborate in the design and development of study documents including data collection forms and manual of procedures. Updates research documents as required during the course of the study. Participate in the construction of electronic data capture of data forms and creation of data checks; performs data management and quality control of study databases. Conducts study training and certification for clinical research staff. Assists with ordering and shipping of central study supplies to the clinical centers. Assists with the review and tracking of documentation for the single Institutional Review Board. Manages study website content (posting and updating study documents). Creates reports to monitor recruitment and protocol adherence. Organizes participates and prepares minutes for study calls and meetings. Acts as a liaison with the clinical center research coordinators. Prepares study reports for the Steering Committee and Data and Safety Monitoring Board. Collaborates with biostatisticians and medical investigators on the primary and secondary analyses; assists with the preparation of abstracts presentations and manuscripts. Performs other related duties as assigned. The omission of specific duties does not preclude the supervisor from assigning duties that are logically related to the position.
Minimum Qualifications
Qualified candidates will hold a masters degree and 1 year of experience in a related discipline. Degree must be conferred by the start date of the position.
Preferred Qualifications
Strong verbal and written communication skills Strong organizational skills Attention to detail Ability to work independently and collaboratively with a team as well as the capacity to work on multiple tasks on short notice Proficiency with Microsoft Word Excel PowerPoint Experience with SAS and R Experience with EDC systems such as OpenClinica Experience with webinar platforms
Work Schedule
MondayFriday 9am6pm
The Biostatistics Center of the Milken Institute School of Public Health is an offcampus research facility of The George Washington University located in Rockville Maryland. The Biostatistics Center serves as the coordinating center for large scale multicenter clinical trials and epidemiological studies funded by federal agencies including the National Institutes of Health. The Biostatistics Center is a leader in the statistical coordination of major medical research programs of national and international scope. Visit our website at: . The Biostatistics Center is seeking a fulltime Research Associate to work as a project manager of the data coordinating center team supporting the NIH funded MaternalFetal Medicine Units Network. Multiple clinical trials evaluating interventions to reduce adverse maternal and neonatal outcomes will be implemented in the next few years. The Research Associate will be responsible for providing study project management throughout phases of a clinical study including implementation conduct closeout and reporting. This position compiles results and prepares technical reports and documentation of outcomes. This role is familiar with standard concepts practices and procedures within a particular field. Working under general supervision this position typically reports to a Principal Investigator. Essential duties include: Maintains daily oversight of study activities and tasks list ensuring timely completion. Collaborate in the design and development of study documents including data collection forms and manual of procedures. Updates research documents as required during the course of the study. Participate in the construction of electronic data capture of data forms and creation of data checks; performs data management and quality control of study databases. Conducts study training and certification for clinical research staff. Assists with ordering and shipping of central study supplies to the clinical centers. Assists with the review and tracking of documentation for the single Institutional Review Board. Manages study website content (posting and updating study documents). Creates reports to monitor recruitment and protocol adherence. Organizes participates and prepares minutes for study calls and meetings. Acts as a liaison with the clinical center research coordinators. Prepares study reports for the Steering Committee and Data and Safety Monitoring Board. Collaborates with biostatisticians and medical investigators on the primary and secondary analyses; assists with the preparation of abstracts presentations and manuscripts. Performs other related duties as assigned. The omission of specific duties does not preclude the supervisor from assigning duties that are logically related to the position.
Minimum Qualifications
Qualified candidates will hold a masters degree and 1 year of experience in a related discipline. Degree must be conferred by the start date of the position.
Preferred Qualifications
Strong verbal and written communication skills Strong organizational skills Attention to detail Ability to work independently and collaboratively with a team as well as the capacity to work on multiple tasks on short notice Proficiency with Microsoft Word Excel PowerPoint Experience with SAS and R Experience with EDC systems such as OpenClinica Experience with webinar platforms
Work Schedule
MondayFriday 9am6pm
Required Experience:
IC
Employment Type
Full-Time
Key Skills
Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.
