161 Jobs in Durham, NC
PSI CRO is Hiring a Clinical Trial Administrator Near Durham, NC
Company Description
PSI is a leading Contract Research Organization with almost 28 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description
Site Management
- Under supervision, exchanges data, documents and other project relevant information between investigative sites, site vendors and the project team
- Under supervision, may assist with clinical supplies (including medication) order, receipt, inventory storage, distribution, return/recall and reconciliation
- Under supervision, supports CA submissions and notifications
- Under supervision, assists with handling administrative financial tasks
- Under supervision, may assist with preparation and follow-up of site, TMF and systems´ audits and inspections
Other Communication
- Under supervision, exchanges data, documents, and other information with the project team and other departments
- Under supervision, provides assistance with organization of internal team meetings
- Under supervision, prepares draft minutes of internal team meetings
- Under supervision, assists with preparation, attendance and follow-up of Investigator’s Meetings, as applicable
- Under supervision, maintains study-specific and corporate tracking systems
Document Management
- Under supervision, maintains Trial Master File (TMF)
- Under supervision, may perform TMF review and oversight at country and site level
- Under supervision, prepares, distributes, and updates Onsite Study Files (OSF) and OSF checklists
- Under supervision, provides assistance with translations
Safety Management
- Under supervision, may assist with safety information flow between investigative sites and the project team
- Corporate/Departmental Assignments
- Under supervision, may provide administrative assistance with feasibility research
Other Assistance
- Provides miscellaneous administrative project support (if applicable)
Qualifications
College or university degree or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities is considered sufficient.
- Basic proficiency in MS Word
- Basic proficiency in MS Excel
- Basic proficiency in MS Outlook
- Basic proficiency in MS Power Point
- Basic proficiency in Skype for Business
- Knowledge (following proper training) of applicable software and project specific systems
- Basic typing skills in English (min. 40 words per minute)
Additional Information
All your information will be kept confidential according to EEO guidelines.
Job Summary
Full Time
$54k-70k (estimate)
04/25/2024
06/23/2024
The job skills required for Clinical Trial Administrator include Innovation, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Trial Administrator. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Trial Administrator. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Clinical Trial Administrator positions, which can be used as a reference in future career path planning. As a Clinical Trial Administrator, it can be promoted into senior positions as a Clinical Research Associate II that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Trial Administrator. You can explore the career advancement for a Clinical Trial Administrator below and select your interested title to get hiring information.
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