Jacqueline Marelia Email & Phone Number | Results-driven accomplished professional in the Pharmaceutical industry with a focus on global submission document coordination in support of clinical and nonclinical regulatory FDA submissions: Investigators Brochure (IB), First Time in Human (FTIH), Biologics License Applications (BLA), Clinical Trial Applications (CTA), Investigational New Drug (IND), Marketed Authorisation Application (MAA), New Drug Application (NDA), and Financial Disclosure Packages. Experience with CRO management, & in-license initiatives in support of regulatory submissions. Proven track record in leading and overseeing many process improvement initiatives to ensure alignment change as well as streamline and improve productivity to meet global needs. Able to take initiative, improve processes, & meet time-sensitive deadlines. Specialties: Professional: • Clinical & nonclinical regulatory submission requirements • Training design and roll-out • Evaluating system effectiveness and stream-lining processes to simplify operating models

Jacqueline Marelia

Results-driven accomplished professional in the Pharmaceutical industry with a focus on global submi...
Greater Philadelphia, Greater Philadelphia, United States

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Jacqueline Marelia’s Email jacqueline.marelia@bms.com

Jacqueline Marelia’s Phone Numbers

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Jacqueline Marelia’s Location Greater Philadelphia, Greater Philadelphia, United States

Jacqueline Marelia’s Current Industry Bristol Myers Squibb

Jacqueline Marelia’s Prior Industry Doylestown Health | Private Company | Glaxosmithkline | Diversified Pharmaceutical Services

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Work Experience

Bristol Myers Squibb

Manager, Global Development Operations (GDO) Submissions at Bristol Myers Squibb

2021-01-01 00:00:00 - Present

Doylestown Health

Emergency Department Pre Service Representative

2017-04-01 00:00:00 - 2019-08-01 00:00:00

Private Company

Not currently seeking job opportunities.

2014-07-01 00:00:00 - 2017-04-01 00:00:00

Glaxosmithkline

CMC Submission Specialist, Global Regulatory Affairs

1996-11-01 00:00:00 - 2014-06-01 00:00:00

Diversified Pharmaceutical Services

CSR, Reserve Operations Specialist, Training assistant

1996-11-01 00:00:00 - 1998-03-01 00:00:00

Skills

No Skills Available

Languages

No Languages Available

FAQ About Jacqueline Marelia

Jacqueline Marelia is located at
Greater Philadelphia, Greater Philadelphia, United States

Jacqueline Marelia is a Results-driven accomplished professional in the Pharmaceutical industry with a focus on global submission document coordination in support of clinical and nonclinical regulatory FDA submissions: Investigators Brochure (IB), First Time in Human (FTIH), Biologics License Applications (BLA), Clinical Trial Applications (CTA), Investigational New Drug (IND), Marketed Authorisation Application (MAA), New Drug Application (NDA), and Financial Disclosure Packages. Experience with CRO management, & in-license initiatives in support of regulatory submissions. Proven track record in leading and overseeing many process improvement initiatives to ensure alignment change as well as streamline and improve productivity to meet global needs. Able to take initiative, improve processes, & meet time-sensitive deadlines. Specialties: Professional: • Clinical & nonclinical regulatory submission requirements • Training design and roll-out • Evaluating system effectiveness and stream-lining processes to simplify operating models

Jacqueline Marelia currently works in the Bristol Myers Squibb |

No Languages Available

Jacqueline Marelia has prior
experience in the following industries:
Doylestown Health | Private Company | Glaxosmithkline | Diversified Pharmaceutical Services

Jacqueline Marelia has the following professional experience:
Bristol Myers Squibb | Doylestown Health | Private Company | Glaxosmithkline | Diversified Pharmaceutical Services