Job Description
Currently to our CoSourse team we are looking for Experience d Clinical Research Assistant.
About the role:
- Provide clerical support for clinical projects according to Client Standard Operating
Procedures (SOPs).
- Maintain administrative systems (tracking and other) for clinical projects according to Client
SOPs.
- Assume a coordinating role for the project team concerning administrative matters.
- Provide telephone coverage and related support duties.
- Set up and maintain clinical investigator files and documentation.
- Prepare investigator budget payments and tracking systems; generate tracking reports as
assigned.
- Data entry and maintenance of selected study tracking databases.
- Prepare monitoring visit documentation for Clinical Research Assistants and above, as
requested by supervisor.
- Prepare study-related documents and other materials for delivery to archives, at appropriate
intervals.
- Perform other administrative duties as assigned by management.
About the role:
- Provide clerical support for clinical projects according to Client Standard Operating
Procedures (SOPs).
- Maintain administrative systems (tracking and other) for clinical projects according to Client
SOPs.
- Assume a coordinating role for the project team concerning administrative matters.
- Provide telephone coverage and related support duties.
- Set up and maintain clinical investigator files and documentation.
- Prepare investigator budget payments and tracking systems; generate tracking reports as
assigned.
- Data entry and maintenance of selected study tracking databases.
- Prepare monitoring visit documentation for Clinical Research Assistants and above, as
requested by supervisor.
- Prepare study-related documents and other materials for delivery to archives, at appropriate
intervals.
- Perform other administrative duties as assigned by management.
Requirements
About You:
- Diploma – Secondary Education or equivalent
- 1-2 year of office Experience (expected 2 or equivalent training).
- Previous clinical trial Experience strongly preferred
- Aptitude for handling and proofreading numerical data. Some spreadsheet software
competency.
- Good oral and written communication skills.
- Good organizational and time management skills.
- Computer literacy (word processing and spreadsheet software).
- Good typing skills.
- Good spelling and proofreading skills.
- Aptitude for handling and reviewing numerical data.
- Ability to operate standard office equipment (e.g., fax, copier).
- Works efficiently and effectively in a matrix environment.
- Fluent in local office language and in English, both written and verbal.
Company offers
THERE IS NO BETTER TIME TO JOIN US!
Education/Qualifications .
Experience .
EEO Employer Covance is committed to diversity in the workplace and is an equal opportunity
employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy
are important to us.
Regional, LTU
Regional, Lithuania
Apply URL: http://jobsearch.covance.com/jobs/1151922-Clinical-Research-Assistant.aspx
