Senior Clinical Research Coordinator

Job description

JOB DESCRIPTION:

About Abbott

Abbott is a global healthcare leader, we are committed to helping people live their best possible life through the power of health. For more than 135 years, we have brought new products and technologies to the world:  in diagnostics, nutrition, cardiovascular, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life.

Today our 115,000 Abbott colleagues are working to help people live not just longer, but better, in the more than 160 countries we serve.

The Opportunity

Our Rapid and Molecular Diagnostics division currently has an opportunity for clinical research coordinator in Galway, Co Galway, Ireland.

PURPOSE OF THE JOB:

The Clinical Research Coordinator supports clinical study activities by assisting with domestic and international studies undertaken by Abbott in support of research and development. This may include the coordination of clinical studies, support for Veeva CTMS, eTMF, studies invoices tracking, clinical documentation maintenance, and shipping of required study supplies and management of internal biological sample inventories.

MAJOR RESPONSIBILITIES:

·  Provide business administrative support for clinical studies and sites management in Veeva CTMS. Support study teams for filing study documents in TMF. Create studies, sites and site personnel in Veeva, support team access to different studies, help troubleshoot and provide support for training.
·   Assist in the filing of required study documentation, including but not limited to study logs, study binders, and regulatory documents according to applicable SOPs.
·  Support tracking of studies and sites level budget, purchase orders and invoices. Assist with creating a new vendor in the procurement system.
·  Coordinate compliant shipments of biological samples, investigational devices and other applicable study supplies.
·  Inventory, ship, track and log all supplies and devices in support of clinical studies. Facilitate final accountability of all clinical supplies and devices.
·  Inventory the receipt of biological samples and populate a database to track the disposition of samples.
·  Coordinate in-house blood draws and internal sample collection studies. Maintain internal sample study administration in accordance with IRB requirements, HIPAA privacy and all applicable regulations.
·  Maintain clinical study activities in spreadsheet templates, consistent with company timelines and objectives.
·  Construct in-house and study site clinical files.
·  Support all clinical affairs activities as needed.

EDUCATION & COMPETENCIES:

·  Previous experience with Veeva CTMS and TMF is preferred.
·  Strong organizational and interpersonal skills required.
·  PowerPoint, Excel, Word and other computer skills necessary.
·  BA/BS (chemistry, biology or other science preferred) and 1-3 years’ experience in clinical study support and/or in biotechnology or related industry preferred.

Connect with us at  www.abbott.com or https://www.ie.abbott/ , on LinkedIn at www.linkedin.com/company/abbott-/ , on Facebook at  www.facebook.com/Abbott  and on Twitter @AbbottNews .

     

The base pay for this position is
N/A

In specific locations, the pay range may vary from the range posted.

     

JOB FAMILY:

Quality Assurance

     

DIVISION:

IDDM ARDx Infectious Disease Developed Markets

        

LOCATION:

Ireland > Galway : Parkmore East Business Park

     

ADDITIONAL LOCATIONS:

     

WORK SHIFT:

Ie - 37.5Hst0 (Ireland)

     

TRAVEL:

Not specified

     

MEDICAL SURVEILLANCE:

No

     

SIGNIFICANT WORK ACTIVITIES:

Not Applicable