Description
Kelly® Science & Clinical is seeking a remote Clinical Data Coordinator for a long-term, contract position at a leading Oncology research group. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Position: Clinical Data Coordinator
Location: US-Remote Based
Pay Rate: $30-35/hr plus Full Benefits
Overview:
The Clinical Data Coordinator would be responsible for clinical data entry activities for the protocols and projects as directed. The position will ensure the highest standards for clinical data integrity and quality are maintained in alignment with critical research efforts aimed to improve the treatment, health and medical outcomes for oncology patients. Responsible for the collection and review of clinical protocol research data; Interpretation of data (including appropriate source documentation) for entry into computerized databases; Good understanding of data definitions and case report forms and other information related to data collection for clinical research. Must respond to queries in a timely fashion.
Main Responsibilities:
- Responsible for the abstraction, entry, and general management of study data for clinical trials.
- Assists with collection, entering, cleaning, maintenance and reporting of clinical research data
- Enters protocol, medical history, and demographic information abstracted from patient charts into appropriate data capturing system (EDC)
- Follow protocol design to assure all protocol data elements are collected in accordance with protocol guidelines
- Update the EDC following verification of subject data, including the resolution of data queries
- Track site goals and case report form completion.
- Maintain study specific documentation.
- Perform QC audits of the clinical database.
- Support and adhere to Good Clinical Practices (GCP) guidelines, FDA, Institutional Review Board (IRB) and HIPAA regulations, Site Operating Procedures and ethical standards for the conduct of research clinical trials.
- Maintain to LLS and Site requirements for source document management and request for information.
- Communicate effectively with the research team, investigator(s), Clinical Research Associate(s), study sponsor and ancillary staff.
Qualifications Required:
- Position requires 3+ years of experience in data collection activities within a GCP/clinical research regulatory environment.
- Education: High School required, some college preferred
- Knowledgeable in critical elements for success in clinical trials. GCPs, ICH, and Code of Federal Regulations.
- Clinical study experience in Oncology required, at least 6 months experience (Myeloma experience a plus)
- Strong medical terminology understanding.
- Experience with Medidata EDC systems. At least 6 months experience
- Proficient in Microsoft Office Suite.
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly
Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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