Sr. Clinical Research Associate

Follow your aspirations to Abbott for diverse opportunities, competitive salaries, great benefits, a 401(k) retirement savings plan, a company paid pension plan and profit sharing, all with a company providing the growth and strength to build your future.
Plan Phase I to IV clinical studies. Assist with study design development and develop protocols and CRFs. Select investigative sites. Monitor/co-monitor clinical sites to ensure adherence to the protocol and compliance with GCP and ICH Guidelines. Coordinate investigator meetings and contract preparation. Assist with management of studies including management of CROs/vendors, essential document handling, trip report review and approval. Assist with maintenance of proper clinical drug supplies. Assist in report writing, including involvement in data interpretation and preparation of reports for regulatory submissions and scientific publications. Assist in planning and maintaining study budgets. Mentor, coach and train junior staff.Qualifications
Excellent verbal and written communication skills. Able to work well under deadline pressure and in a team environment. Able to negotiate workable solutions to complex problems involving multiple parties. High performing CRA with experience across multiple compounds, multiple indications, and multiple study phases. Experience monitoring multiple study sites. Minimum three years of CRA experience. Experience with study/site audits. Experience with preparing portions of INDs, NDAs, and/or Investigator Brochures.
Bachelors Degree; Bachelors Degree in Science preferred

${abbott.description.certifications}Abbott welcomes and encourages diversity in our workforce. EEO/AATo apply for this position, click on the Apply Now buttonTo learn more about Abbott and view other opportunities, please visit: http://www.abbott.com/career/career_center.cfm
REQUIREMENTS
Please see Job Description