Research Associate

About the job

Primary Duties And Responsibilities

Understand and interpret clinical trial study protocols to design and develop calendars. Understand and interpret clinical trial agreements and sponsor budgets to develop site budgets for the protocol.

Design and develop case report forms for clinical trial study protocols

Develop a familiarity with Advarras Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software to utilize related functionalities in the design and development of calendars budgets financials and case report forms.

Work closely with reporting manager to complete daily/ weekly calendars budgets financials and/or case report forms design to meet with predetermined quality criteria.

Understand and utilize internal case management software and other reporting software to ensure that daily/weekly work assignments are appropriately tracked and completed.

Actively participate in team meetings and contribute meaningfully to discussions related to specific customer cases and/or protocols.

Position Requirements:

Knowledge of clinical research methodology industry regulations and Good Clinical Practice guidelines related to human research.

Expected to work independently as well as in a team environment.

Good organizational and administrative abilities

Familiarity with MS Office and various business software

Preferred: 01 year work experience in job areas such as: o Clinical trial coordinator at site

Clinical data management

Pharmacovigilance

Records management

Key Personal Attributes:

Highly personable nature that fosters teamwork

Excellent communication skills oral as well as written

High energy and positive attitude towards working in a culturally diverse environment

A passion for ensuring outstanding customer support with a solutionsoriented attitude.

Proactive and takes ownership in all tasks from starttofinish.

Please use the below link for job application and quicker response.

Remote Work :

No