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Clinical_Solutions_Group Jobs & Careers

62 Jobs Found

Clinical Solutions Group, Inc (CSG) provides global clinical research solutions and FSP services to the pharmaceutical, biotechnology, and medical device industries. Administrative Assistant is responsible for providing daily support via phone, e......
Clinical Solutions Group, Inc. has partnered with a large pharmaceutical client in the Greater Philadelphia area to fill an immediate need for a experienced Statistical Programmer. A qualified candidate will meet these basic basic standards; Requi......
•Possess experience creating SAS datasets, generating TLGs/reports, validating other programmers' output, adhering to CDISC standards, developing macros, etc. •Apply knowledge of the CDISC Standards, SDTM and ADaM. •Create derived datasets in ac......
- Responsible for statistical aspects of clinical and pre-clinical research projects including study design, sample size estimation, patient randomization, case report form development, writing statistical analysis plans, statistical analysis and in......
1. Identify errors/inconsistencies in CRF data 2. Ensuring their resolutions in order that databases can be declared clean and locked according to strict performance standards. 3. Review and contribute to the development of trial validation plan r......
• Review protocols for proper data capture including case report form design • Assist Data Manager on development of eCRF specifications and review according to the protocol • Maintain in-house trials which could include (develop programming, test......
Skills: Budget, Clinical Outsourcing, Contract, contract terms and conditions A managing position providing leadership during the contract management and negotiation process to ensure ethical, fair and compliant practices are followed when developi......
The Clinical Trial Manager (CTM) is responsible for the successful planning, management, oversight and execution of clinical trials and the associated work packages in Clinical Operations. The span of activities is broad covering clinical activitie......
•Expert in Oracle Inform Central Designer for forms and rules development for study setup and post go live changes •Define eCRF, DVS and dataset specifications for a given protocol. •Provide oversight of vendors for defined eCRF specification •Defin......
The individual shall provide programming expertise and technical for a Phase I-IV Data Management Technical Support team. Key responsibilities and skills include, but are not limited to, the following: Developing and validating study dataset specifi......
1. Provide statistical support for publications, presentations, posters at medical meetings and any other requests not covered in the clinical study report. T 2. Under the direction of the lead statistician for clinical trials (Phase I to IV), provi......
1. Provide programming expertise and technical for a Phase I-IV Data Management Technical Support team. 2. Develop and validate study dataset specifications against sponsor libraries and vendor deliverables, CDISC/SDTM review of vendor deliverable......