Accountable for the scientific integrity of the study and the well-being of patients in clinical trials
Apply technical and clinical skills to ensure efficient and high-quality clinical trials
Responsible for effective execution of studies and works closely with clinical and medical colleagues
Author and manage approval of Informed Consent Documents (ICDs)
Establish Data Monitoring Committees (DMCs) and endpoint adjudication committees
Track and reconcile serious adverse events (SAEs) across a study

Requirements

Advanced degree or professional certification in a health care related, scientific or technical discipline required
5+ years of experience and track record of success in biopharmaceutical industry in clinical research and development
Clinical research experience in phase 3/pivotal space
Extensive knowledge of clinical development, global and regional regulation, ICH/GCP, adverse event management
Demonstrated clinical, administrative, and project management capabilities, as well as excellent verbal and written communication skills in English
Demonstrated experience establishing, managing, and training teams in clinical development

Benefits

401(k) plan with Pfizer Matching Contributions
Additional Pfizer Retirement Savings Contribution
Paid vacation
Holiday and personal days
Paid caregiver/parental and medical leave
Health benefits to include medical, prescription drug, dental and vision coverage

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

clinical trialsInformed Consent DocumentsData Monitoring Committeesadverse event managementclinical researchclinical developmentproject managementregulatory complianceICHGCP

Soft Skills

communication skillsadministrative capabilitiesteam managementtrainingleadershiporganizational skillscollaborationproblem-solvingattention to detailinterpersonal skills

Certifications

advanced degreeprofessional certification