Description :
Responsible for assisting in ensuring that new interventional global clinical trials are registered and clinical study results are posted to public databases such as ClinicalTrials.gov and PhRMA ClinicalStudyResults.org, and that PhRMA, guidelines and applicable laws are adhered to. Assists in maintaining all active registrations and results disclosures; ensures accurate and complete data (including collection of information and data entry). Develops and maintains strong internal relationships and acts as liaison with the clinical teams, legal, public affairs, investor relations, and regulatory intelligence as needed to ensure appropriate compliance. Assisting with maintaining master listing of interventional clinical trials. Assisting with maintaining metrics for Clinical Trials Registration and Results Disclosure (CTR/RD) area. Assisting with developing and implementing policies, procedures, processes and training for CTR/RD area. Experience Level: 0-3 years Degree Required: Bachelor's