Elise Givant Email & Phone Number | I have been involved with clinical research since 1987. I have held many positions including: Study coordinator, CRO field monitor, Lead CRA and Clinical Team Lead across Phase I to Phase IV drug studies. I have been responsible for site management and management of clinical monitoring activities from pre-study site visits through study close-out for phase I, II and III studies in the US and globally. I have also monitored phase I, II, III and IV clinical trials across a wide spectrum of therapeutic specialties including: Oncology: Prostate, Renal Cell, Colorectal, Breast, including adjuvant breast cancer, Pancreatic, Head and Neck, Lung (NSCL, SCL), Melanoma, Hypercalcemia, Bone Metastases, Supportive care: Anti-Emetic, Pain, Hematology: Leukemia (ALL, CML, CMML, AML, MDS), Lymphoma (NHL), and Multiple Myeloma. Rheumatology and Osteoarthritis, Medical Device for BPH I have managed global and North American studies with monitoring activities in up to 3 countries. Responsibilities have spanned the full duration of studies and have included early protocol development, presentations at Investigator Meetings, maintaining verbal and written communications with numerous study sites, interaction with various departments, including Regulatory Affairs, Medical Archives and Grants Administration. As a Sr. Clinical Project Manager, I apply this expertise and leadership toward large, complex investigative trials, and serves as a resource for newer CTLs and CRAs.

Elise Givant

I have been involved with clinical research since 1987. I have held many positions including: Study...
Harrisburg, Pennsylvania, United States

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Elise Givant’s Location Harrisburg, Pennsylvania, United States

Elise Givant’s Current Industry Hersheypark

Elise Givant’s Prior Industry Synteracthcr | Quintilesims | Inc Research

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Retired

2022-05-01 00:00:00 - Present

Senior Clinical Trial Manager

2017-07-01 00:00:00 - 2022-07-01 00:00:00

Senior Clinical Study Manager

2007-08-01 00:00:00 - 2013-08-01 00:00:00

Clinical Team Leader and Line Manager

2001-11-01 00:00:00 - 2007-08-01 00:00:00

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Elise Givant is a I have been involved with clinical research since 1987. I have held many positions including: Study coordinator, CRO field monitor, Lead CRA and Clinical Team Lead across Phase I to Phase IV drug studies. I have been responsible for site management and management of clinical monitoring activities from pre-study site visits through study close-out for phase I, II and III studies in the US and globally. I have also monitored phase I, II, III and IV clinical trials across a wide spectrum of therapeutic specialties including: Oncology: Prostate, Renal Cell, Colorectal, Breast, including adjuvant breast cancer, Pancreatic, Head and Neck, Lung (NSCL, SCL), Melanoma, Hypercalcemia, Bone Metastases, Supportive care: Anti-Emetic, Pain, Hematology: Leukemia (ALL, CML, CMML, AML, MDS), Lymphoma (NHL), and Multiple Myeloma. Rheumatology and Osteoarthritis, Medical Device for BPH I have managed global and North American studies with monitoring activities in up to 3 countries. Responsibilities have spanned the full duration of studies and have included early protocol development, presentations at Investigator Meetings, maintaining verbal and written communications with numerous study sites, interaction with various departments, including Regulatory Affairs, Medical Archives and Grants Administration. As a Sr. Clinical Project Manager, I apply this expertise and leadership toward large, complex investigative trials, and serves as a resource for newer CTLs and CRAs.