Associate Clinical Research Specialist Jobs in Texas

5+ years of CRA experience.

3+ years of experience working on oncology studies.

BS in a relevant scientific discipline.

Ability to travel and be on-site. (Austin, TX or Portland, OR).

6-month contract. - 40 hours per week. - Monday to Friday.

Austin, TX or Portland, OR

Knowledge of project management tools and practices, and proficiency in using normal office software; Microsoft Word, Excel and PowerPoint.

Participate in maintaining accuracy within clinical management systems and internal reports and trackers.

Able to manage multiple projects independently and use varying databases and management systems.

Minimum 1-3 years relevant clinical research experience.

Excellent verbal and written communication skills, good organizational and interpersonal skills, and a team drive.

Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with industry best practices.

Two years of relevant experience.

Supports daily operations for a research study or clinical trial.

Recruits, screens, and enrolls study participants; ensures participant adherence to study protocol.

Collects, evaluates, enters, and tracks data.

Submits data, study documents, and/or reports to regulatory agencies.

Assists with completion of protocol-specific documents.

Participates in adverse event reporting and safety responsibilities monitoring.

May participate in adverse event reporting and safety responsibilities monitoring.

Knowledge of regulations governing medical devices is desirable.

Career development with an international company where you can grow the career you dream of.

Free medical coverage for employees* via the Health Investment Plan (HIP) PPO

An excellent retirement savings plan with high employer contribution

Knowledge of Federal and State regulatory issues/mandates concerning Institutional Review Board requirements

This position has potential to work remotely (must live in California).

Two years’ experience with Word, Excel and Internet access/use

Previous experience with clinical research

BS/BA degree in health sciences or related field

Formal training in decision support, databases, spreadsheet, report writer, query/relational database computer software applications