Clinical Data ManagerWe are seeking a detail-oriented Clinical Data Manager to oversee the collection, validation, management, and integrity of clinical trial data. The ideal candidate will ensure that clinical study data is accurate, complete, and compliant with regulatory requirements while collaborating with cross-functional teams to support successful clinical research.Key Responsibilities:Design, develop, and maintain clinical databases for clinical trials.Create and review Case Report Forms (CRFs) and electronic CRFs (eCRFs).Perform data validation, data cleaning, and discrepancy management.Develop and execute Data Management Plans (DMPs).Coordinate database setup, user acceptance testing (UAT), and database lock activities.Review data queries and work with clinical sites to resolve discrepancies.Ensure compliance with GCP, ICH, FDA, and applicable regulatory guidelines.Collaborate with Clinical Operations, Biostatistics, Medical Writing, and Programming teams.Monitor data quality metrics and generate status reports.Support audit and inspection readiness by maintaining complete documentation.Manage external vendors such as Electronic Data Capture (EDC) providers when required.Participate in study start-up, conduct, and close-out activities.Required Qualifications:Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Computer Science, or a related field.3+ years of experience in clinical data management.Experience with Electronic Data Capture (EDC) systems such as Medidata Rave, Oracle InForm, REDCap, or Veeva.Strong knowledge of CDISC standards (SDTM, CDASH).Understanding of ICH-GCP, FDA, and clinical research regulations.Experience with data validation, query management, and database lock procedures.Excellent analytical, organizational, and problem-solving skills.Strong written and verbal communication skills.Preferred Qualifications:Certification in Clinical Data Management (CCDM) is a plus.Experience working with CROs or pharmaceutical companies.Knowledge of SAS, SQL, or clinical reporting tools.Familiarity with risk-based monitoring and data quality management.Experience supporting global, multi-site clinical trials.Technical Skills:Electronic Data Capture (EDC) SystemsMedidata RaveOracle InFormREDCapVeeva VaultSASSQLMicrosoft ExcelClinical Trial Management Systems (CTMS)Soft Skills:Strong attention to detailCritical thinkingProblem-solvingTime managementTeam collaborationCommunication skillsDocumentation skillsOrganizational abilitiesPreferred Certifications:Certified Clinical Data Manager (CCDM)Good Clinical Practice (GCP) CertificationBenefits:Competitive salaryHealth, dental, and vision insurancePaid time offRetirement savings planProfessional development opportunitiesFlexible work arrangementsEmployee wellness programsThis job description is optimized for candidates with experience in clinical data management, EDC systems, regulatory compliance, and clinical trial data quality assurance.
...work as assigned. Specifically tied to NRC regulations includes the control of reactivity systems that affect power levels of the plant. Monitoring gauges, dials, or other indicators to make sure a machine/system are working properly. Controlling operations of...
...through programs, services, and educational opportunities. Our staff includes positions such as administration, clinicians, nurses, teachers, case managers, psychiatrists, and direct support providers who work within our 15 facilities to support over 3,000 individuals...
...Architectural Drafter NAGEL Architects + Engineers has an opportunity for an Architectural Drafter to join our team! NAGEL is a growing Architecture and Engineering firm looking for a confident, experienced design professional with a passion for excellence in the...
...HBA Construction in Kalamazoo, MI is seeking a Siding Installer / Exterior Construction Carpenter for full-time work. The role involves installing various exterior products like siding, windows, and doors on residential homes. Ideal candidates should have reliable transportation...
...Job Title Summary: Work Mode: Onsite Location: Plymouth, MN Responsibilities: Produce high-quality medical devices within a manufacturing cell. Perform detailed assembly and operation of various equipment and machinery per documented procedures....