Par Pharmaceutical Work Values

Daily Duties at Par Pharmaceutical:

Accountable for the setup, quality and maintenance of the electronic Trial Master Files (TMF) in accordance with SOPs. Performs ongoing reviews of TMF to assure quality of the documentation files

What they like about Par Pharmaceutical:

The social vibrance of a hiring firm is very important to you. Your ability to make and maintain friendships there is a critical part of your decision. You would likely be dissatisfied with a workplace that is quiet, cold, or otherwise not particularly social. When you investigate a new hiring company, ask recruiters, managers, and potential co-workers about the social life and opportunities there. This is especially important when you are relocating; moving dramatically alters your social sphere both inside and outside the workplace.

Tags

clinical research, in house clinical research associate, Clinical research project management, in house site monitoring, oncology study management, CTMS , TMF, clinical research site management, Pre-Study, Site Initiation, Site monitoring, Site close-out, clinical research in house

Skills

• In depth protocol knowledge and deep understanding of concepts of clinical research and drug development, • Familiarity with medical terminology, FDA regulations, ICH and GCP guidelines, • Expertise in maintaining the TMF for the study, • Ability to diffuse and resolve issues at investigative site and maintain communication link with study team., • Assist in preparation of binders for the sites (Regulatory, Pharmacy) as required, • Excellent planning, project management and analytical skills , • Excellent verbal, written communications skills, interpersonal and organizational skills

These are some of the questions we asked our climbers about their experiences with Par Pharmaceutical: