Seeking someone with no clinical research experience but a sciences/medical background in school (Biology, Kinesiology, Exercise Science, Health Sciences, etc.). Good for an MA/Phlebotomist with medical terminology experience. Also good for someone who has experience with EMR systems. Job DescriptionThis position is a clinical research data coordinator role with the Phase One cancer research team in medical oncology. You will work on the team dedicated to pharmaceutical clinical trials for patients who are in a Phase 1 cancer trial. This position is responsible for evaluating and interpreting collected clinical data in conjunction with the Principal Investigator (PI) as appropriate. You will prepare oral or written presentations or reports and analyses setting forth progress trends and provide recommendations or conclusions. Additionally, you will collect clinical data under clinical research protocols, taking data obtained from patients and research coordinators on the team and entering it into a database selected by the sponsor of the trial. There will be multiple databases due to the number of studies with different pharmaceutical sponsors. You will be assigned a pool of trials to work on solely, getting to know the ins and outs of the trial/data system. Meeting deadlines for data entry will be crucial. You will also become familiar with the patients and feel connected to them through your work.Hard Skills
organization and prioritization
clinical trial data entry
timeline management
Job TypeThis is a Contract-to-Hire position with a duration of 6 Month(s).Work SiteThis is a hybrid position requiring some days on-site in St. Louis, Missouri and some days remote.Work EnvironmentThis position will be part work from home and part on-site. On-site work will be 2 days a week, and work from home will be 3 days per week. The hours are normal business hours, Monday through Friday. While on-site, you will work in a cubicle environment near your team members. There are 8 other data coordinators on the Phase 1 team, and they are adding one more due to an influx of new studies. You will be assigned studies based on workload and will work with different clinic coordinators for each study. There are no set pairs of data coordinators and clinic coordinators.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.
