- job summary: Job Description The Medical Writing Intern (MWI) assists with medical writing activities in support of the GCDO - Medical Writing & Transparency department. The MWI works closely with MW personnel to develop regulatory documents in support of company products. This individual will work to assigned timelines, communicate effectively to the responsible medical writer, and ensure their deliverables are completed according to appropriate qualityjob summary: Job Description The Medical Writing Intern (MWI) assists with medical writing activities in support of the GCDO - Medical Writing & Transparency department. The MWI works closely with MW personnel to develop regulatory documents in support of company products. This individual will work to assigned timelines, communicate effectively to the responsible medical writer, and ensure their deliverables are completed according to appropriate quality
- job summary: Responsibilities Technical Lead aligned to modernization/data service strategy Qualifications modernization/data service strategy location: Malvern, Pennsylvania job type: Contract salary: $56.73 - 61.73 per hour work hours: 8am to 5pm education: Bachelors responsibilities: Responsibilities Technical Lead aligned to modernization/data service strategy Qualifications modernization/data service strategy qualifijob summary: Responsibilities Technical Lead aligned to modernization/data service strategy Qualifications modernization/data service strategy location: Malvern, Pennsylvania job type: Contract salary: $56.73 - 61.73 per hour work hours: 8am to 5pm education: Bachelors responsibilities: Responsibilities Technical Lead aligned to modernization/data service strategy Qualifications modernization/data service strategy qualifi
- job summary: Required: Must be currently enrolled in a Bachelor's degree program (Junior/Senior level)No industry experience requiredStrong verbal and written communication skillsBasic knowledge of Word, Excel, PowerPoint, and shared platforms (e.g., SharePoint, Box, Smartsheets) Preferred: Exposure to Good Clinical Practices (GCP) regulations and Standard Operating Procedures (SOPs)Understanding of clinical study phases and their role in clinicaljob summary: Required: Must be currently enrolled in a Bachelor's degree program (Junior/Senior level)No industry experience requiredStrong verbal and written communication skillsBasic knowledge of Word, Excel, PowerPoint, and shared platforms (e.g., SharePoint, Box, Smartsheets) Preferred: Exposure to Good Clinical Practices (GCP) regulations and Standard Operating Procedures (SOPs)Understanding of clinical study phases and their role in clinical
- job summary: This position will be in the Analytical Support Section of the Quality Control Department which consists of eleven team members working together to support the department goals. The main activities of the role are as follows: - QC Test Material Management - International Shipments - new product support - compendial compliance - method transfers - method validation - support Assay Lifecyle Program The main responsibilities will be to support tjob summary: This position will be in the Analytical Support Section of the Quality Control Department which consists of eleven team members working together to support the department goals. The main activities of the role are as follows: - QC Test Material Management - International Shipments - new product support - compendial compliance - method transfers - method validation - support Assay Lifecyle Program The main responsibilities will be to support t
- job summary: Shift: M-F 8-4:30PM; Fully onsite position This position will be in the Analytical Support Section of the Quality Control Department which consists of eleven team members working together to support the department goals. The main activities of the role are as follows: QC Test Material ManagementInternational ShipmentsNew product supportCompendial complianceMethod transfersMethod validationSupport Assay Lifecyle Program The main responjob summary: Shift: M-F 8-4:30PM; Fully onsite position This position will be in the Analytical Support Section of the Quality Control Department which consists of eleven team members working together to support the department goals. The main activities of the role are as follows: QC Test Material ManagementInternational ShipmentsNew product supportCompendial complianceMethod transfersMethod validationSupport Assay Lifecyle Program The main respon
- job summary: Responsibilities Working with other data scientists on the team to develop AI/ML solutions in the legal/compliance domain.Leveraging a broad range of techniques. location: Malvern, Pennsylvania job type: Contract salary: $65.08 - 70.08 per hour work hours: 8am to 5pm education: Bachelors responsibilities: Working with other data scientists on the team to develop AI/ML solutions in the legal/compliance domain.Leveraging ajob summary: Responsibilities Working with other data scientists on the team to develop AI/ML solutions in the legal/compliance domain.Leveraging a broad range of techniques. location: Malvern, Pennsylvania job type: Contract salary: $65.08 - 70.08 per hour work hours: 8am to 5pm education: Bachelors responsibilities: Working with other data scientists on the team to develop AI/ML solutions in the legal/compliance domain.Leveraging a
