Will Watts Email & Phone Number

Dallas, Tx, Us

Santa Monica, California, Us

Santa Monica, California, Us

Santa Monica, California, Us

• Familiar with routine medical/scientific terminology• Help to maintain internal Clinical Operations databases and document repositories• Provides assistance in site selection, study implementation and ongoing coordination of study sites.• Assist setting up, organize and maintain clinical study documentation (e.g. Trial Master Files) including preparation for internal/external audits, final reconciliation and archival• Assist in preparation and development of protocols, informed consents, monitoring plans and other study related plans.• Review case report forms, abstracts, presentations, manuscripts and clinical study reports.• Assist in resolving routine monitoring issues• Proactively identifies potential operational challenges and in collaboration with senior team members provides solutions to ensure study execution remains on track• Assists in preparation of safety, interim and final study reports, including resolving data discrepancies• Assists with Investigator Meeting coordination, activities preparation and where required review meeting minutes

Clinical Trial Specialist on the Breast Cancer Clinical Trial Unit. Experienced with Phase I - Phase III Protocols, Regulatory Affairs, Good Clinical Practice, HIPPA, Data Entry/Data Monitoring guidelines, and IRB Regulations.

Birmingham, Al, Us

• Bacterial Culture, Mammalian Cell Culture• Transformation, Transfection• Protein Isolation and Purification • Agarose/Acrylamide Gel Electrophoresis • Member of team that studied the role of RANK:Traf-2 interaction in breast cancer metastasis• Assessed RANK: Traf-2 interaction using immunofluorescence and Western blot• Member of team that developed an ELISA test for speed and endurance in race horses• Developed ELISA test to assess the level of GDF-8 expression in horse serum• Developed a SNP multiplex PCR genetic predisposition test for speed and endurance in race horses

Durham, North Carolina, Us

Data Monitor• Extensively trained on cognitive test data on traditional measures and proprietary endpoints for schizophrenia • Broad understanding of GCP’s, IRB requirements and FDA regulations for current studies • Advisor to new employees training them on data review and certifications• Communicate/Query clinical raters for clarification on assessments• Assist in the creation/writing of SOP’s for new projects• Enter data into the EDC from assessments received • Oversee creation of score reports and Data Entry of T-Scores• Clean/Verify data entry for assessments receivedCertification Specialist• Assesses rater qualifications for certification on cognitive batteries• Interviews raters individually; discerning assessment administration and scoring competence • Documents interview and rater’s abilities demonstrated• Provides the Project Lead with documentation of certification status

Biotechnology Regulatory Affairs Certification, Regulatory Affairs

Master'S Of Science, Biotechnology

Bachelor Of Science - Bs, Biology, General