Fiona Campbell Email & Phone Number | Senior scientist with over 20 years experienced with leadership, clinical, medical, regulatory and quality experience in the bio-pharmaceutical and medical device industries. Affiliate (local country), Area (regional) and Global Brand Team exposure in medical affairs. Proven ability to create and drive clinical research to meet and exceed targets. Extensive experience of implementing and leading industry and investigator led clinical studies. Strong background in international clinical, PV, and regulatory compliance requirements. Proven ability to form relationships and influence External Experts (EE) and regulators. Experience presenting to Peers, EEs, International Congress symposia, and FDA (CBER) scientific committees and advisory boards. Effective verbal and written communicator. Flexible. Ability to multitask and respond to changing priorities and timelines. Strong attention to detail, research analytical and leadership skills. Proven project management skills.

Fiona Campbell

Senior scientist with over 20 years experienced with leadership, clinical, medical, regulatory and q...
Ireland

*50 free lookup(s) per month.

Fiona Campbell’s Phone Numbers

Get FIONA’s Phone Number (For Free)

Social Media

Fiona Campbell’s Location Ireland

Fiona Campbell’s Current Industry Iqvia

Find accurate emails & phone numbers for over 700M professionals.

Director Drug Development Lead

2022-08-01 00:00:00 - Present

Medical Manager

2021-05-01 00:00:00 - 2022-08-01 00:00:00

Clinical Industry Liason Officer

2018-12-01 00:00:00 - 2021-05-01 00:00:00

Available for employment

2018-05-01 00:00:00 - 2018-12-01 00:00:00

Senior medical advisor vaccines

2016-06-01 00:00:00 - 2018-05-01 00:00:00

AREA Medical Advisor Abbvie

2012-08-01 00:00:00 - 2015-10-01 00:00:00

Virology Medical manager

2009-04-01 00:00:00 - 2012-07-01 00:00:00

No Skills Available

No Languages Available

Fiona Campbell is a Senior scientist with over 20 years experienced with leadership, clinical, medical, regulatory and quality experience in the bio-pharmaceutical and medical device industries. Affiliate (local country), Area (regional) and Global Brand Team exposure in medical affairs. Proven ability to create and drive clinical research to meet and exceed targets. Extensive experience of implementing and leading industry and investigator led clinical studies. Strong background in international clinical, PV, and regulatory compliance requirements. Proven ability to form relationships and influence External Experts (EE) and regulators. Experience presenting to Peers, EEs, International Congress symposia, and FDA (CBER) scientific committees and advisory boards. Effective verbal and written communicator. Flexible. Ability to multitask and respond to changing priorities and timelines. Strong attention to detail, research analytical and leadership skills. Proven project management skills.