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25 days old

Senior Clinical Research Coordinator/Site Lead - Glendale, AZ

Kelly Services
Glendale, AZ 85304
**Senior Clinical Research Coordinator/Site Lead - Glendale, AZ**



The Clinical Research Coordinator, Senior who will function as the day-to-day operational leader for a team of clinical research staff in overseeing and participating in the coordination, conduct and evaluation of clinical research, and apply knowledge of clinical research to the program population.



The Clinical Research Coordinator, Senior will work under the supervision of the Regional Medical Director to provide project coordination and clinical research daily operations for this multi-site program to ensure successful implementation of and adherence to the clinical research protocol, locally approved protocol practices and standard procedures, and national and local milestones regarding planning, administration, timeline management, enrollment, participant engagement and retention, data collection, quality biospecimen processing, and reporting.



This position will require travel to one or more sites within this metro area on a regular basis. With notice, occasional travel to our other primary sites and, less frequently, out-of-state travel may be required.



**Duties & Responsibilities:**




+ Qualifying talent will be evaluated on their demonstrated experience and competence in clinical research, clinical dexterity, and problem-solving. Able to perform and train the employees on the following duties:

+ Maintain awareness of status of all active studies. Collaborate with investigator(s) and coworkers to ensure proper progress and completion of clinical studies.

+ Conduct pre-consent screening to determine eligibility.

+ Execute the informed consent process according to Good Clinical Practice (GCP) and procedures and other applicable rules, regulations and policies.

+ Ensure participant and study compliance, i.e. collection of study specimens, and study visits.

+ Collect and process samples in accordance with the protocol, manual of operations, standard operating procedures (SOP) or other work instruction set.

+ Ensure specimens are properly logged, handled and stored.

+ Perform data cleaning procedures and quality checks to ensure accuracy of data. Support the data-management process for clinical research projects, including addressing data queries from data managers, project statistician, and sponsors. Review reports, tables, and listings.

+ Work with study team as needed to define specimen collection, processing and storage procedures.

+ Periodically self-audit records to ensure audit-readiness.

+ Oversee and follow through on questions and issues that arise during study conduct.

+ Train others as needed to collect and label samples as instructed and deliver or process samples in accordance with the protocol, manual of operations, standard operating procedures (SOP) or other work instruction set.

+ Proactively identify and monitor barriers to recruitment and problem-solve or innovate to overcome them.

+ Determine best method/s to identify potential participants for research protocol (advertisements, chart reviews, monitoring of clinic schedule, etc.) and prepare accordingly.

+ Prepare, submit & maintain all regulatory submissions (proposed new studies, annual review, amendments, & adverse events) accurately & within a timely manner to all collaborative parties.

+ Apply legal, regulatory & policy parameters to promote ethical practices in research involving human participants & to ensure compliance to those regulations.

+ Knowledge, Skills, & Abilities

+ Maintain knowledge of the principles, practices and techniques of research clinical skills.

+ Motivated to provide high quality, compliant research.

+ Skill in maintaining detailed records.

+ Desire to build new program and develop new policies.

+ Ability to work both independently and with a team, resolving issues with a positive outcome.

+ High level of integrity, ethics and professionalism.

+ Strong communication and computer skills.

+ Strong organization skills and significant attention to detail for data entry.



**Minimum Qualifications:**




+ Bachelors degree in a field appropriate to the area of assignment and four (4) years related research experience OR Masters degree in a field appropriate to the area of assignment AND three (3) years of related experience OR Eight (8) years equivalent combination of experience in research, training and/or education approved by Human Resources.

+ Two (2) years experience training, leading or supervising employees.

+ Fully trained in Phlebotomy.

+ Experience with clinical research protocols, development, implementation and regulations.

+ Motivated to provide high quality, compliant research.

+ Fluent in speaking, reading and writing Spanish.

+ CCRP/CCRC certification



**APPLY TODAY! Have Questions? Email at kevin.lau@kellyscientific.com**






**Why Kelly** **** **?**



With Kelly, youll have access to some of the worlds highest regarded scientific organizationsproviding you with opportunities to work on todays most challenging, research-intensive, and relevant projects. Our connections can lead you to innovative scientific pursuits youll be proud to help advance. We work with 90 of the Fortune 100 companies and found opportunities for more than 10,000 scientific professionals last year.


You pursued a career in science to fuel your quest for knowledge and your desire to make the world a better place. Let Kelly fuel your careerconnect with us today.




**About Kelly** ****



At Kelly, were always thinking about whats next and advising job seekers on new ways of working to reach their full potential. In fact, were a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live. Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.


Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law. at https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm

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Posted: 2019-12-30 Expires: 2020-01-30

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Senior Clinical Research Coordinator/Site Lead - Glendale, AZ

Kelly Services
Glendale, AZ 85304

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