Clinical Research Coordinator II
Actalent
Job Title: Clinical Research Coordinator IIJob Description
Coordinate, implement, and evaluate clinical research trials, studies, and projects. Provide direction in the development of research protocols, recruit and screen potential study participants, and develop and conduct patient and family education. Oversee financial accounts to ensure operations remain within approved levels, perform patient evaluations, administer medications, and provide nursing support for specialized diagnostic, therapeutic, and surgical procedures. Make referrals to in-house or community professionals and serve as a clinical resource. Collect data, assist in developing data collection systems, and compile reports. Provide direction and support to other Research Coordinators or support members. Perform related responsibilities as required.
Responsibilities
+ Independently manage significant and key aspects of Oncology-related trials including one or more small trials or research projects.
+ Operate as Oncology Research Coordinator in support of specified Oncology disease group(s).
+ Perform required patient consents.
+ Train and provide guidance to less experienced staff.
+ Oversee data management for research projects.
+ Interface with research participants and resolve issues related to study protocols.
+ Authorize purchases for supplies and equipment maintenance.
+ Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials.
+ Periodically audit operations including laboratory procedures to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes.
+ Monitor IRB submissions and respond to requests and questions.
+ Interface with study sponsors, monitor and report SAEs; resolve study queries.
+ Provide leadership in determining, recommending, and implementing improvements to policies/processes.
+ Assist in developing grant proposals and protocols.
+ With appropriate credentialing and training, perform phlebotomy, specimen collection, or diagnostics.
+ Perform some supervisory duties as needed.
+ Perform related approved responsibilities as required.
Essential Skills
+ Good Clinical Practice (GCP) knowledge
+ Patient consenting
+ Clinical Research Coordinator (CRC) experience
+ SAE reporting
+ 2+ years of solid CRC experience in oncology or interventional drug trials in other therapeutic areas
+ Experience reporting AE/SAE within NIH and Pharma-funded trials where drugs were dispensed
+ Oncology experience
+ Certified Clinical Research Coordinator (CCRC)
+ Case Report Form (CRF) knowledge
+ Informed Consent Form (ICF) knowledge
Additional Skills & Qualifications
+ High School Diploma or GED and 3+ years of clinical research experience
+ Two years of college in a scientific, health-related, or business administration program and three years clinical research experience
Work Environment
Office-based in a hospital clinic setting. The work schedule is Monday to Friday, 8 AM to 5 PM. There may be occasional requirements to visit downtown Atlanta sites due to being high enrolling locations.
Pay and Benefits
The pay range for this position is $28.00 - $30.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision• Critical Illness, Accident, and Hospital• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available• Life Insurance (Voluntary Life & AD&D for the employee and dependents)• Short and long-term disability• Health Spending Account (HSA)• Transportation benefits• Employee Assistance Program• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Johns Creek,GA.
Application Deadline
This position is anticipated to close on Feb 19, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
+ Hiring diverse talent
+ Maintaining an inclusive environment through persistent self-reflection
+ Building a culture of care, engagement, and recognition with clear outcomes
+ Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
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