SR Clinical Research Associate- Project Manager

  • Location
    Stanford , California
  • Category
    Medical & Science - Research
  • Job type
    Contract/Temporary


Adecco Medical & Science is seeking a SR Clinical Research Associates-Project Manager to work in the beautiful city of Palo Alto, CA! This SR Clinical Associate Project Manager offers a great opportunity to join an company which culture values collaboration, Innovation and evidence-based operations. Your mission is to innovate, support and promote high impact global reaching clinical research to improve human health!



Primary responsibilities for a SR Clinical Research Associate-Project Manager are:

Familiar with clinical trial stage process and ability to management a team of 10 or more employees
Facilitates and coordinates the daily activities for clinical studies (including recruiting and scheduling study subjects) and plays a critical role in the conduct of the study
Working closely with the clinical operations department and participates in the informed consent process by communicating clearly and openly with potential study patients about protocols open to enrollment.
Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol(s)
Reviews and comprehends each assigned protocol including study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections
Assists with data entry, database management and study materials including but not limited to case report forms (CRFs), enrollment logs, signature and delegation logs, training logs and investigational device accountability logs
Coordinates with the clinical operations department to help ensure that clinical research and related activities are performed in accordance with Federal regulations, and Verily policies and procedures
Works collaboratively with the other members of the Verily research team and the clinical operations department and other supporting teams to ensure all protocols are followed and that there is timely documentation and submission of study data






QUALIFICATIONS:

Bachelor’s Degree in health or biologic science (Masters-level degree strongly preferred)
5-7 years in a clinical research setting, preferably working as a clinical research coordinator on Industry-Sponsored clinical trials.
5-7 years of clinical trial project management experience (Preferred)
Expert Knowledge of Good Clinical Practice/ICH, FDA, HIPAA policies
Site monitoring and clinical quality compliance experience



Great benefit plans offered! This is an outstanding Full-Time direct hire opportunity! Annual salary DOE!


For all qualified SR Clinical Research Associate-Project Managers, please respond with your resume in word format and a date/time availability for a phone interview by the COB October 3rd, 2017! For other opportunities available at Adecco Medical and Science go to www.adeccousa.com. If you have questions about the position, please contact Dorian Baker at 925-349-0310 or dorian.baker@adeccona.com

Adecco is an equal opportunity employer and strictly prohibits unlawful discrimination based upon an individual race, color, religion, gender, sexual orientation, gender identity / expression, national origin/ ancestry, age, mental/ physical ability, medical condition, marital status, veteran, or any status, or any other characteristic protected by law.


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Reference number US_EN_2_108218_319922