Clinical Research Coordinator

  • Location
    Mountain View , California
  • Category
    Medical & Science - Nursing
  • Job type
    Contract/Temporary


Adecco Engineering and Technical has a current job opportunity for Clinical Research Coordinator

JOB REQUIREMENTS:
Under the direction and supervision of the Verily clinical staff, this position facilitates all implementation phases of new clinical studies as well as the ongoing coordination and maintenance of open and closed studies. The position arranges and oversees all clinical trial activities and plays a key role in assisting in patient recruitment for clinical studies. The position works closely with the Principal Investigator, members of the clinical operations department, monitors, and clinicians, to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of all ongoing clinical studies.

Top 3 Daily Responsibilities:
- 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)

Additional Responsibilities
- 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


To be considered for this position, please contact Anthony Williams at (925) 349-0308 or at anthony.williams@adeccona.com.



Required Skills
- Bachelor’s Degree in health or biologic science (BS/BA/ BScN or higher) is required
- Two years in a clinical research setting, preferably working as a clinical research coordinator on Industry-Sponsored clinical trials.
- Knowledge of Good Clinical Practice/ICH, FDA, HIPAA policies
- Ability to prioritize quickly and appropriately

Nice to have
- Masters-level degree is preferred
- Site monitoring and clinical quality compliance experience
- Ophthalmology/Optometry experience preferred
- Experience working for a startup

This position will be located in Palo Alto for on a permanant and we have a contract opportunity available.

  • Apply with Adecco

Reference number US_EN_2_108218_319867