Research Associate
General Summary To support the development of clinical research services that enhance research effectiveness and timelines, and which are specific to...
General Summary
To support the development of clinical research services that enhance research effectiveness and timelines, and which are specific to the software applications (Clinical Trial Management Software as well as Electronic Data Capture software) of Advarra Solutions.
Primary Duties and Responsibilities
- Understand and interpret clinical trial study protocols in order to design and develop calendars for schedule of events
- Design and develop case report forms for clinical trial study protocols
- Develop a familiarity with Forte's Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software to utilize related functionalities in the design and development of calendars and case report forms.
- Work closely with reporting manager to complete daily/ weekly calendars and/or case report forms design to meet with pre-determined quality criteria.
- Understand and utilize internal case management software and other reporting software to ensure that daily/weekly work assignments are appropriately tracked.
- Actively participate in team meetings and contribute meaningfully to discussions related to specific customer cases and/or protocols.
Position Requirements:
Minimum qualification: Degree in Life sciences/related fields.
1-2 years of clinical research coordinator or site coordinator experience. Past oncology experience will be of an additional advantage.
Must have participated in preparation and management of clinical research budgets and monetary disbursements, including subject payments and sponsor invoicing.
Expected to work independently, as well as in a team environment
Good organizational and administrative abilities.
Sound knowledge & efficiency in computer programs - MS word, PowerPoint, Excel etc.
Key Personal Attributes:
Highly personable nature that fosters team work
Excellent communication skills - oral as well as written
High energy and positive attitude towards working in a culturally diverse environment
Self-motivated and proactive
Working Hours:
Monday-Friday 9:00 a.m. to 6:00 p.m.
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