Pharmanet Inc. Work Values

Daily Duties at Pharmanet Inc.:

Performed site recrutiment, site selection and drug closeout for several pharmaceutical companies, Monitored 15 sites in a Phase IIIB Randomized Double Blind diabetes clinical trial for Takeda pharmaceuticals., Designed monitoring conventions for a diabetes clinical trial, Monitored an ankjylosing spondylitis trial with Immunex for Embrel, Reviewed projecty related materials for completeness, Assisted in investigator recruitment and evaluations of site selection, Monitored initial, interim and closeout visits for all protocols and all sites. Peformed query resolutions and resolved CRF discrepancies. Performed drug accountability at site visits, Reported adverse events promptly to sponsor and obtained clarification of data. Verified completenss of critical documents, Monitored regulatory file at site visits for completeness. Participated at the investigator meetings, Created study team tools for the ankylosing spondylitis trial.

What they like about Pharmanet Inc.:

A hiring company that offers alternative approaches to pay, performance bonuses, and/or equity in the firm is very attractive to you. You're generally less interested in working for an organization offering only traditional, salary-based compensation, one with limited opportunity to acquire equity in the firm, or one that does not actively promote skill development. In addition, you are more likely to choose a company that offers a variety of internal career options, with defined career paths. You view the learning of new skills and development of your expertise as key to your career advancement. These aspects of an organization may become even more important to you as you progress in your field, and are especially critical if you change career or occupation.

Tags

pharmacovigilance, Sr. clinical research associate, Immunology, Oncology, Virology, Endocrinology, Cardiac markers, Data reconciliation, Clinical trials, Global delivery, Protocol development, Medical case management, Risk management, Clinical narratives, SAE reporting, Medical devices, IND queries, Regulatory reporting, Global unblinding, Safety database, Adverse event reporting, 21 CFR ICH, MedRa coding, WHO dictionary, IND reports, Regulatory submissions, Clinical study reports, Perodic Safety Update Reports PSUR, Quality auditing, Site Management, Monitoring, Teaching adults, Investigator meetings, Regulatory compliance, Internet recruiting, Drug development, Query resolution, Triage case workload, Oracle Argus II

Skills

These are some of the questions we asked our climbers about their experiences with Pharmanet Inc.: