**Clinical Documentation Specialist** Clinical Oklahoma City, OK, US Pay Rate Low: 24.00 | Pay Rate High: 34.00 + Added - 05/02/2025 Apply for Job We are looking to hire a Clinical Documentation Specialist at a contract manufacturing company specializing in the production of therapeutic proteins and antibodies to manufacture drugs for its clients clinical trials. **Clinical Documentation Specialist** **6 Month Contract to hire** **$24.00-$34.00 per hour** **Essential Duties and Responsibilities:** + Support day-to-day Process Characterization activities, authoring/reviewing these documents in various stages of completion + Organization of documentation, electronic and hardcopy + Document archiving (scanning, and per PC work instruction) + Ensures documentation through logbooks and batch records + Data entry or analysis for risk assessment and experimental designs + Data entry verification, Hands-on project execution including biophysical and physiochemical assays + Participate in meetings, presentations and conduct training **Job Requirements:** + BS/MS preferred in biochemistry or related science + 2+ years of experience in Biotechnology or CMO/CRO is preferred + Familiarity and exposure to GLP, cGMP, and regulatory requirements. + Exposure to a range of protein analytical techniques, for examples, ELISA, HPLC, enzymatic, and electrophoretic (SDS-PAGE, Western blots, IEF, & CE) procedures + Hands-on biophysical analysis (DLS, SLS, Lab Chip, MALS) is preferred This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH \#LI-DNP: We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.