Ophthalmic Research Associates Work Values

Daily Duties at Ophthalmic Research Associates:

Clinical Trial Operations • Writing and review of clinical study protocols • Preparation of clinical study documents including consent forms, screening scripts, source documents etc. • Submission of documents for IRB approval • Collection of clinical data and transcription of data from source document to CRF • Basic statistical analysis and interpretation of trial data • Participation in meetings and calls with sponsors • Vendor management Research and Development • Developed a new clinical research model for allergic inflammation • Researched and developed clinical and exploratory endpoints • Research on novel targets for drug development Medical Writing • Writing and review of articles for trade journals • Narrative writing and power point presentations • Assist in writing pre-IND, IND and clinical study reports • Review of scientific literature • Review of manuscripts for peer-review journals

What they like about Ophthalmic Research Associates:

A hiring company that offers alternative approaches to pay, performance bonuses, and/or equity in the firm is very attractive to you. You're generally less interested in working for an organization offering only traditional, salary-based compensation, one with limited opportunity to acquire equity in the firm, or one that does not actively promote skill development. In addition, you are more likely to choose a company that offers a variety of internal career options, with defined career paths. You view the learning of new skills and development of your expertise as key to your career advancement. These aspects of an organization may become even more important to you as you progress in your field, and are especially critical if you change career or occupation.

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Skills

These are some of the questions we asked our climbers about their experiences with Ophthalmic Research Associates: