Our client is searching for a mechanic with experience working on various PLCs, HMIs and other machinery! The ideal candidate has multiple years of maintenance experience and is eager to find a long term home. Great benefits from day one as well as a sign on bonus! If interested please read more and apply below!salary: $60,000 - $72,000 per yearshift: Firstwork hours: 7 AM - 3:30 PMeducation: High SchoolResponsibilities Maintenance: Monitor equi
Our client is searching for a mechanic with experience working on various PLCs, HMIs and other machinery! The ideal candidate has multiple years of maintenance experience and is eager to find a long term home. Great benefits from day one as well as a sign on bonus! If interested please read more and apply below!salary: $60,000 - $72,000 per yearshift: Firstwork hours: 7 AM - 3:30 PMeducation: High SchoolResponsibilities Maintenance: Monitor equi
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 quality
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 quality
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 clinical
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 clinical
Are you a dynamic account executive who enjoys fostering client relations, helping companies grow their business, and are looking to help others in your field!? We are seeking a full time sales person to work in the NE territory! Preferably located in the Philadelphia area, but not a must. This is a permanent hire with the comany, NOT contract! Connect with me if you are interested and feel you would be a good fit!salary: $35,000 - $38,500 per ye
Are you a dynamic account executive who enjoys fostering client relations, helping companies grow their business, and are looking to help others in your field!? We are seeking a full time sales person to work in the NE territory! Preferably located in the Philadelphia area, but not a must. This is a permanent hire with the comany, NOT contract! Connect with me if you are interested and feel you would be a good fit!salary: $35,000 - $38,500 per ye
job summary: The CRA will be responsible for monitoring oversight, co-monitoring, and site management work to ensure that the CRAs working under the CRO(s) and the sites conducting the studies on behalf of Company, follow all applicable regulations, guidelines, and sponsor requirements. The CRA will work closely with study teams, investigators, and research sites to ensure the successful execution of clinical trials from start up through close out. Ideall
job summary: The CRA will be responsible for monitoring oversight, co-monitoring, and site management work to ensure that the CRAs working under the CRO(s) and the sites conducting the studies on behalf of Company, follow all applicable regulations, guidelines, and sponsor requirements. The CRA will work closely with study teams, investigators, and research sites to ensure the successful execution of clinical trials from start up through close out. Ideall
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