Clinical Research Associate
Requisition ID: 50321
Position: Full-Time Regular
Functional area: Clinical
Location: Portland, Oregon
Los Angeles, California
Required degrees: Bachelors Degree
Relocation: No
Basic qualifications:
- 4 Year BS/BA Degree with 4-5 years site monitoring or equivalent experience preferred.
- Effective communication skills (oral and written)
- Strong computer skills; experience with electronic data capture preferred.
- Ability to proactively identify and interpret problems, recommend creative solutions, and influence appropriate changes.
- Awareness of site dynamics and ability to effectively interact with, motivate, and education site personnel.
- Ability to work independently and be a self-starter.
- Complex problem-solving and decision-making skills.
- Accomplished time management and organizational skills.
- Flexibility and adaptability.
- Must live in assigned geographical area. No relocation available.
Preferred qualifications:
- Understanding of therapeutic area of assigned development compounds.
- Aware of clinical program strategy and goals and importance of study timelines to meet these goals.
Details:
- Create a local culture of accountability, continual learning, best practice sharing and process standardization.
- Demonstrated outstanding verbal and written communication skills and abilities, including small and large group presentations.
- Demonstrated excellent IT proficiencies; MS Programs:
Excel, Word, PowerPoint, EDM Systems, Lotus Notes or similar e-mail
program, database utilizations, and web-sharing software.
- Proven success with working in a field-based office environment.
- Ability to work independently and meet deadlines.
- Demonstrated ability to effectively work with
investigational study site personnel with clinical trial experience
strongly preferred.
- Excellent organizational skills.
- Experienced in the initiation and monitoring of clinical trials per ICH/FDA Guidelines.
- Effectively conduct site assessment/new recruitment efforts.
- Demonstrated ability to work within a matrix organization.
- Experienced in site development and management: setup, monitoring, closeout activities in the conduct of clinical trials.
- Demonstrated knowledge of scientific methodology in design and conduct of clinical trials.
- Excellent working knowledge of Good Clinical Practice (GCP) regulations.
To apply, send cover letter and resume to info@ncwebcenter.com
