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Clinical Research Manager -Phoenix, AZ

Kelly Services


Location:
Phoenix, AZ
Date:
04/18/2018
2018-04-182018-05-17
Job Code:
US15TPKL_BH1421428
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Job Details

Job Title Clinical Research Manager -Phoenix, AZ

Jobid US15TPKL_BH1421428

Location: Phoenix, AZ, 85067, USA

Description **Clinical Research Manager - Phoenix, AZ**

Every day Kelly Scientific Resources (KSR) connects scientific professionals with opportunities to advance their careers. We currently have an exciting opportunity for a Clinical Reserach Manager to work with an establish company in Phoenix, AZ.


The Clinical Research Manager will report to the Associate Director of Clinical Research Operations and provide operational and supervisory support for this multi-site study to ensure successful implementation of and adherence to the clinical research protocol and national and local milestones regarding planning, administration, timeline management, scheduling of coordinators, enrollment, participant engagement, data collection, and reporting.

The Clinical Research Manager will be responsible for clinical research operations at assigned sites, including working closely with colleagues, as well as adherence to enrollment metrics and milestones, and supervision and training of clinical research coordinator staff who are involved in enrollment, informed consent, study procedures, data collection and documentation, and interactions with the study team and clinical partners.

**Responsibilities:**


+ Supervise clinical research staff for all aspects of conducting a complex and multi-site clinical study.
+ Develop and implement plans, schedules, and standard operating procedures under the guidance of study leadership for assigned sites.
+ Collaborate effectively with others to ensure proper progress in enrollment milestones and completion of studies.
+ Supervise activities of subordinates, if assigned.
+ Participate in local and national collaborative calls related to program operations.
+ Train new staff in preparation and conduct of clinical trials and protocol specific operations.
+ Supervise and provide oversight and guidance as needed to research staff.
+ Collect and process specimens to meet study requirements, including saliva, urine and intravenous blood samples.
+ Coordinate and participate in monitor visits, audits, and quality reviews (internal and external) in a professional manner.
+ On a periodic basis and with notice, adjust regular working schedule to provide weekend or evening enrollment coverage as needed.
+ Provide oversight for the preparation, review, submission and maintenance of regulatory activities/submissions within our team to the national IRB, ensure accuracy and timeliness of distributing regulatory updates to all collaborative parties.
+ Implement successful plan to identify potential participants.
+ Prepare study staff and participate directly in recruitment/enrollment.
+ Determine best method/s to identify potential participants for research protocol (advertisements, chart reviews, monitoring of clinic schedule, etc.) and prepare accordingly.
+ Maintain a detailed tracking system for participants considered for enrollment. Track progress at regular intervals and report out to PI and study team.
+ Proactively take initiative to ensure enrollment stays on track with the project timelines.
+ Communicate with participants and families in culturally sensitive manner.
+ Compose clear, precise and detailed correspondence.
+ Develop a rapport with study participants.
+ Communicate study-related issues to investigators, sponsors, coordinating centers, study coordinators, clinical team, managers and other institutions in a timely fashion.
+ Oversee data entry and validation to ensure accuracy, quality and compliance of data collection process.
+ Maintain master files for clinical research protocols.
+ Ensure quality of data submitted from study sites and assure timely submission of data.
+ Assist other members by educating, providing resources and consulting on difficult protocols or projects.
**Minimum Requirements:**


+ Masters or Bachleors in Life Sciences
+ 2 plus years of supervising exprience
+ Current Certified Clinical Research Professional (CCRP) status.
+ Strong organization skills and significant attention to detail for data entry.
+ Self-motivated, willing and able take initiative.
+ 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.
APPLY TODAY! Have Questions? Call Kevin at 602-548-1774 or email at kevin.lau@kellyscientific.com

**Why Kelly** **®** **?**


With Kelly, you’ll have access to some of the world’s highest-regarded scientific organizations—providing you with opportunities to work on today’s most challenging, research-intensive, and relevantprojects. Our connections can lead you to innovative scientific pursuits you’ll be proud to helpadvance. We work with 95 of the Fortune 100™ companies, and found opportunities for more than 9,000scientific professionals last year.

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

**AboutKelly Services** **®**

As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2017 was $5.4 billion. Visit kellyservices.com and connectwith us on Facebook , LinkedIn and Twitter .

Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females,Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and iscommitted to employing a diverse workforce. Equal Employment Opportunityis The Law.



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