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You will be updated with latest job alerts via emailThe Clinical Project Intern provides administrative and clinical support to Clinical Study Management (CSM) personnel aiding in project organization and for clinical studies. Responsibilities include supporting Clinical Research Associates (CRAs) in monitoring activities managing Essential Documents maintaining Investigator Site Files updating databases and assisting CRAs during site visits. This role also participates in meetings manages mail and courier requests.
Responsibilities:
The Clinical Project Assistant (CPA) provides administrative and clinical management support to CSM personnel and assist them with the inhouse organization management and of projects and activities undertaken by the CSM personnel assigned to clinical studies conducted within the country.
If applicable supports CRAs with preparations for monitoring activities as necessary.
Supports local Clinical Team with the handling of Essential Documents. Ensures the Investigator Site Files are created contain the correct and complete documentation and are shipped as appropriate to the Investigational Sites.
May be assigned as the local updater of databases (such as Clinical Trial Management Systems) with Country related data. If applicable assists inhouse CRAs during site visits (administrative tasks point of contact etc..
Actively participates in relevant Meetings manages the collection and distribution of mail and courier requests and may act as a local liaison for CRO (Observational) Studies.
Qualifications :
Preferred background in lifescience or healthcare related qualification or experience is desired.
Preferred prior experience and basic knowledge related to ICH/GCP Guidelines and applicable local regulations.
Basic awareness of the conduct of clinical trials and its associated activities and responsibilities.
Previous administrative experience is desired.
Ability to manage multiple priorities/projects communication and interpersonal skills.
Proactive and positive team player.
Written and verbal fluency in English.
Proven ability to communicate effectively within a multicultural/global team environment.
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Fulltime
Full-time