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Apply online for the
Clinical Research Associate
position and advance your career in the
Pharmaceutical industry today.
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Clinical Research Associate : GlaxoSmithKline
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| Job Number |
58166 |
| Employee Type |
Full Time |
| Company Name |
GlaxoSmithKline |
| Location |
Houston
Texas
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| Salary (year) |
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| Experience |
2 to 5 Years |
| Start Date |
2/17/2010 |
| Industry |
Pharmaceutical |
| Job Type |
Clinical |
| Relocation |
Not Required |
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GlaxoSmithKline
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| Description |
Basic Qualification
4 Year BS/BA Degree with 3+ years site monitoring or equivalent experience preferred.
Must live in assigned geographical area. “No relocation available.”
Details
Up to 75% Travel.
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. |
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| Requirements |
Preferred Qualification
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 educate 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.
Understanding of therapeutic area of assigned development compounds.
Aware of clinical program strategy and goals and importance of study timelines to meet these goals. |
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