Lori Vivian Email & Phone Number | Clinical Operations Professional with a valuable blend of clinical research experience focused in cardiovascular and rare disease, medical drug and device trials, with a nursing background. Expertise in planning, initiating, conducting, monitoring, managing, and completing medical drug and device studies. Extensive knowledge of clinical development operations, focused in good clinical practices (GCP), establishing research processes, managing studies, protocol development, site selection, trial design, monitoring plans, statistical methods, regulatory compliance, and data management. Understanding of regulatory affairs in clinical trial management. Exceptional negotiation, problem-solving, issues management, and communication skills. Experience with multi-center/multi-country studies as well as smaller single country studies. Management style is to empower team members and takes a genuine interest in staff development. Strong sense of urgency, big-picture perspective, attention to detail, and flexibility to work in fast-paced organizations.

Lori Vivian

Clinical Operations Professional with a valuable blend of clinical research experience focused in ca...
Valley City, Ohio, United States

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Lori Vivian’s Email lvivian@syntactx.com

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Lori Vivian’s Location Valley City, Ohio, United States

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Sr. Director, Project Management

2020-11-01 00:00:00 - Present

Director Project Management

2019-11-01 00:00:00 - 2020-11-01 00:00:00

Director, Clinical Project Management

2018-02-01 00:00:00 - 2019-11-01 00:00:00

Associate Director, Global Clinical Research

2015-06-01 00:00:00 - 2018-02-01 00:00:00

Clinical Research

2012-10-01 00:00:00 - 2014-04-01 00:00:00

Director, Clinical Research Operations

2010-06-01 00:00:00 - 2012-09-01 00:00:00

Manager, Vascular Surgery ARO

2005-11-01 00:00:00 - 2010-06-01 00:00:00

CICU RN

1989-06-01 00:00:00 - 1998-08-01 00:00:00

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Lori Vivian is a Clinical Operations Professional with a valuable blend of clinical research experience focused in cardiovascular and rare disease, medical drug and device trials, with a nursing background. Expertise in planning, initiating, conducting, monitoring, managing, and completing medical drug and device studies. Extensive knowledge of clinical development operations, focused in good clinical practices (GCP), establishing research processes, managing studies, protocol development, site selection, trial design, monitoring plans, statistical methods, regulatory compliance, and data management. Understanding of regulatory affairs in clinical trial management. Exceptional negotiation, problem-solving, issues management, and communication skills. Experience with multi-center/multi-country studies as well as smaller single country studies. Management style is to empower team members and takes a genuine interest in staff development. Strong sense of urgency, big-picture perspective, attention to detail, and flexibility to work in fast-paced organizations.

Lori Vivian has prior
experience in the following industries:
Ppd | Iqvia | Inventiv Health Clinical | Clinipace Worldwide | Syntactx | Cleveland Clinic | St Vincent Hospital

Lori Vivian has the following professional experience:
Icon | Ppd | Iqvia | Inventiv Health Clinical | Clinipace Worldwide | Syntactx | Cleveland Clinic | St Vincent Hospital