Matt Didavide

About Matt Didavide

Experienced Senior Recruiter with a demonstrated history of working in the pharmaceuticals industry. Skilled in placing CRA\'s, Managers, Medical Writers and Scientists in Drug, Device and Vaccine research. Strong human resources professional with a Bachelors focused in Health, Criminology and Business from West Chester University of Pennsylvania.

Experience

1. Senior Recruiter, Clinical Research

   kps life

   Feb 2018 — Present · Philadelphia, PA, US

   Responsible for the recruiting process and the successful staffing of positions for permanent and contract resourcing• Provides operational support and focus relative to the recruitment function, acting in collaboration with Managers and Directors at specific locations or business units• Works with Management Team to develop business and staffing requirements, and recruitment strategies and tactics.• Maintains reports of recruiting activity, including projections of future activity• Fills high impact market positions by identifying professional and manager level candidates for openings by making contact by telephone i.e, cold calls as needed • Traveling to various regional offices to work and train with members of the management team• Coordinates offer amounts and compensation packages with hiring managers and site Human Resources• Negotiates compensation packages with potential candidates• Continuously sources applicants for potential openings; maintains a pipeline of qualified individuals• Provides meaningful feedback on candidates to hiring managers for use in the hiring decisions• Presents slate of qualified candidates to hiring managers as open positions are identified• Identifies candidates for key positions, and develops the relationship required to effectively recruit for current or future positions

Education

• West Chester University of Pennsylvania

  Bachelors, Health, Criminology and Business

  1995

Skills

• Ich-Gcp
• Pharmaceutics
• Medical Writing
• Regulatory Submissions
• Clinical Data Management
• Cardiology
• Clinical Trials
• Biotechnology
• Diabetes
• Regulatory Affairs
• Lifesciences
• Pharmacovigilance
• U.s. Food and Drug Administration (Fda)
• Oncology
• Protocol
• Recruiting
• Life Sciences
• Clinical Monitoring
• Clinical Trial Management System (Ctms)
• CRO Management
• Edc
• Good Clinical Practice (Gcp)
• Therapeutic Areas
• Endocrinology
• Ctms
• Infectious Diseases
• Drug Development
• Gcp
• Biopharmaceuticals
• Pharmaceutical Industry
• Sop
• Fda
• Gastroenterology
• Clinical Development
• Standard Operating Procedure (Sop)
• Electronic Data Capture (Edc)
• CRO
• Medical Devices
• Clinical Research
• Neurology