Clinical Project Ιntern

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

The Clinical Project Intern provides administrative and clinical support to Clinical Study Management (CSM) personnel, aiding in project organization and execution 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 in-house organization, management and execution 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.

•Preferred background in life-science or health-care 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 multi-cultural/global team environment.

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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

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