Hiring a medical assistant to help with clinical research studies during the evening shift (M-F 3pm-11pm) Job Responsibilities: Assists Clinical Research Coordinator (CRC) and Investigator with a variety of clinical study activities to provide necessary support in the conduct of a clinical study.
Provide comprehensive Quality Control (QC) activities relating to the completion of source documents and CRFs for the clinical trials conducted at the Clinical Research Center.
Job Requirements: Good computer skills (Word and Excel).
Strong interpersonal skills.
Detail-oriented and strong document review skills.
Be trained or have experience in clinical research GCP requirements and medical documentation requirements.
About Actalent: Actalent connects passion with purpose.
Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more.
Every day, our experts around the globe are making an impact.
Were supporting critical initiatives in engineering and sciences that advance how companies serve the world.
Actalent promotes consultant care and engagement through experiences that enable continuous development.
Our people are the difference.
Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Required Preferred Job Industries Retail