Worldwide Clinical Trials - California

This job posting is no longer available on association of Clinical Research Professionals. Find similar jobs: Cra jobs - Worldwide Clinical Trials jobs

Worldwide Clinical Trials is a therapeutically focused global CRO that provides full-service drug development services to the pharmaceutical and biotechnology industries. As one of the most innovative and scientifically-driven contract research organizations, we offer exceptionally strong clinical trial methodology integrated with an effective global operations network. We are currently seeking highly experienced individuals to join us in the position of Clinical Research Associate and Senior Clinical Research Associate. Positions are nationwide and are regional home based.

RESPONSIBILITIES: Tasks may include but are not limited to: -Perform feasibility studies (pre-study site selection) when required -Conduct all level of monitoring visits in accordance to GCPs and applicable local and international regulations and SOPs. This encompasses clinical trial material (CTM) accountability, regulatory document review and submission (as appropriate), clear and complete trip report writing and site management -Provide mentoring and coaching to colleagues and site staff when needed -Manage/advise teams in therapeutic areas of proficiency as required or appropriate -Design monitoring tools as requested -Provide support for the design of CRFs and protocols as requested -Develop monitoring plans when required -Actively participate in study team meetings -Actively participate in investigator meetings -Conduct training for colleagues or study team as requested -Manage a cost centre and implement appropriate actions to keep within budget (UK and ROW) OTHER SKILLS AND ABILITIES: -Excellent oral and written communication skills -Excellent planning and organizational skills with effective time management -Excellent interpersonal skills -Ability to work logically and methodically -Ability to lead and motivate assigned team (if applicable) -Initiative and problem solving skills -Ability to input into process initiatives, SOPs related to monitoring and site management activities -Good understanding of FDA and /or EU Directive regulations, ICH Guidelines and local regulatory requirements -Thorough understanding of standard operating procedures -Proficient knowledge of Microsoft Office, eCRF, IVRS packages -Thorough understanding of clinical research principles and processREQUIREMENTS: -A minimum four-year college curriculum with a major concentration in biological, physical or health studies and a minimum experience of three years as a Clinical Research Associate-Travel required Within WCT, we offer an excellent salary and employee benefit package to include, but not limited to, medical, dental, vision, flexible spending account, company paid life insurance, voluntary life insurance, short & long term disability, company matching 401K, and comprehensive paid time off. If you have the experience required, and feel you are the dynamic person that we are looking for, please send your resume in a Word document via email to:

association of Clinical Research Professionals - 2 years ago - save job
About this company
17 reviews
About Worldwide Clinical Trials Worldwide Clinical Trials is a global CRO providing full-service drug development services to the...