Clinical Data Manager/Senior Clinical Data Manager, Oncology Looking for 2 people. One is a Senior Level Position and the other is not. Candidates must have the following experience: Clinical Data Manager Candidate needs to have hands-on experience conducting all DM activities and possess some project management skills to manage his/her own project. Experience in InForm, Oncology, or managing global study a plus'. Under minimal supervision, perform all data management functions to ensure timely and quality database lock for studies Phase I-III. Perform data management activities for eDC studies conducted in-house (protocol review, CRF development, database set-up activities, data validation process, external data reconciliation medical coding, SAE reconciliation, etc...). -Bachelor degree or above in scientific or related field; commensurate experience in Data Management may be considered. - Knowledge of I-Review/J-Review a plus. -Proficiency on all related regulations, GCP, and Good Clinical DM Practice. -Computer proficiency and knowledge of medical terminology. Note: For Senior Level Lead Person: Candidates must possess experience as a CDM lead on a trial. Also, the lead candidate must be able to communicate how they measures metrics, generated reports,etc. In addition, both candidates must have hands on experience in the entire study cycle from Start to Finish. Suppliers: your candidates must be able to back up what is on their resume. We strongly suggest you screen and interview your candidates thoroughly and perform reference checking as indicated in your contract. Also advised Suppliers that we want to see longevity in previous positions. Senior Clinical Data Manager Candidate needs to have hands-on experience conducting all DM activities and possess strong project management and excellent interpersonal skills to independently manage a global project. Experience in InForm, Oncology a plus. Independently perform all data management functions to ensure timely and quality database lock for studies Phase I-III. Perform data management activities for EDC studies conducted in-house as well as oversee activities of off-shore CRO handling outsourced projects (protocol review, CRF development, database set-up activities, data validation process; medical coding, SAE reconciliation, etc...). -Bachelor degree or above in scientific or related field; commensurate experience in Data Management may be considered. - Knowledge of I-Review/J-Review a plus. -Proficiency on all related regulations, GCP, and Good Clinical DM Practice. -Computer proficiency and knowledge of medical terminology. -Strong oral and written communication skills SOFT SKILLS: - Seeking candidates who are willing to learn, are motivated, enthusiastic and who are team players. Someone who has an innate ability to take initiative, problem solve, meet deadlines, etc. Note: Suppliers: your candidates must be able to back up what is on their resume. We strongly suggest you screen and interview your candidates thoroughly and perform reference checking as indicated in your contract. Also advised Suppliers that we want to see longevity in previous positions.