EMMANUEL OSONG NOUMBISSIE

E-mail: q4lxj7@r.postjobfree.com

Phone: 240-***-****

My background is epidemiology; I am a motivated graduate and professional with clinical Research knowledge, public health science, and strong organization and management skills.

EDUCATION

Walden University Student, PhD in Public Health – Epidemiology, (Dissertation in progress on Improving Drugs Safety).

Walden University, M.P.H., Masters in Public Health, (2008).

Hood College, B.A., in Biology, (2006).

British College of Buea, B.S., in Computer Science, (2001).

WORK EXPERIENCE

2010 - Present NEOPha, Inc.

CEO & President

• Implements the strategic goals and objectives of the company

• Effectively manages the resources of the company according to authorized policies and procedures that fully conform to current laws and regulations, toward the achievement of the organization's philosophy, mission, strategy, and its annual goals and objectives.

2010 - Present NEOPha, Inc.

Social Media Manager

• Implement the social media strategy, into all of the company’s products and services

• Manage social media campaigns and day-to-day activites. Duties include online advocacy, writing editorial, community-outreach efforts, promotions, etc.

• Manage presence in social networking sites including Facebook, Twitter, and other similar community sites, posting on relevant blogs, and seeding content into social applications as needed

• Advocate the Company in social media spaces, engaging in dialogues and answering questions where appropriate

• Monitor effective benchmarks for measuring the impact of social media programs, and analyze, review, and report on effectiveness of campaigns in an effort to maximize results

• Monitor trends in social media tools, trends and applications

2007 - Present Technical Resources International, Inc.

Safety and Pharmacovigilance Specialist

• Tracks and amends adverse event (AE) reports and abstracts key AEs into databases.

• Prepares and reviews investigator safety reports and notifications for non-Investigational New Drug (IND) AE reports.

• Prepares and reviews investigator safety reports and notifications for Investigational New Drug (IND) AE reports.

• Writes and reviews SOPs and Project Work Instructions for the department.

• Maintains electronic files for the department; and performs queries of Serious Adverse Events (SAE) databases.

• Performs and process queries from Pharmaceutical companies, and maintains electronic files for the department.

• Performs triage and safety review of initial and updated Serious Adverse Event (SAE) and Expedited Adverse Event (EAE) reports received from clinical trial/study sites for internal consistency.

• Determines whether SAE/EAE reports meet the Division of Acquired Immune Deficiency Syndrome (DAIDS) and Food and Drug Administration (FDA) reporting requirements.

• Writes, reviews, and submits Safety reports for non-IND clinical trials/studies for submission to the FDA.

• Performs Clinical site contact on adverse event reportability and drug safety memos to sites and IRB’s.

• Performs file case searches, maintains file room for the department, and use department databases to track and manage and control issued documents. Assign various documents tracking numbers.

2009 - Present Technical Resources International, Inc.

Document Control Manager

• Manage Document control associates.

• Perform file case search and reviews.

• Coordinate the activities of Document control, including distribution and auditing controlled documents, maintenance of electronic department directories, tracking and reporting on document progress to facilitate group activities.

• Review and proofread documents for consistency of document format, tracking numbers and system concerns

• Use department databases to manage, track, and control issued documents.

• Prepare meeting documents, and generate meeting minutes.

• Reports on document progress to facilitate group activities.

• Assign tasks to Document control associates.

Training and Seminars with TRI

• MedDRA trained.

• Clinical Trial Design and Statistical issues

• IND and Clinical Drug Review Process/Issues

• GCP, HSP

• Clinical trials course

• Seminar with NIH/FDA - Ethics in Clinical Trial by

• Seminar with DEA/NIAID/NIH – The AIDS Epidemic Lessons Learned and a Look Ahead.

• CITI - Institutional Training Initiative in Clinical Research Trials

03/2007 – 05/2007 Frederick County Public School System

Substitute Teacher

Supervisor - Elizabeth Huber, 301-***-****

• Lesson plan development and implementation, wrote and implemented behavior management plans, managed educational paperwork, effectively communicated with parents and other staff members.

01/2004– 12/2006 MEO Medical Billing

• Managed Data Entry, Coding, Billing and Filing, Insurance Follow-up, and Customer service

01/2003– 01/2004 BAO Medical Billing

• Managed Data Entry, Coding, Billing and Filing, Insurance Follow-up, and Customer service

COMPUTER SKILLS

Software: Microsoft Office; Microsoft Word, Microsoft Excel, Microsoft PowerPoint, SPSS.

CERTIFICATES

• MedDRA

• GCP

• Protecting Human Research Participants

LAB EXPERIENCE

• DNA isolation and purification

• PCR

• Agarose electophoresis

• Protein extraction and quantitation

• SDS polyacrylamide electophoresis

• Spectophotometric enzyme assays and indirect Immunofluorescence assays

LANGUAGES

English Advanced professional proficiency

(Able to use the language fluently and accurately on all levels. Nearly native ability to read and understand extremely difficult or abstract prose, colloquialisms and slang.)

Pidgin Advanced professional proficiency

(Able to use the language fluently and accurately on all levels. Nearly native ability to read and understand extremely difficult or abstract prose, colloquialisms and slang.)

French General professional proficiency

(Able to speak the language with sufficient structural accuracy and vocabulary to participate effectively in most formal and informal conversations. Able to read within a normal range of speed and with almost complete comprehension.

AWARDS/HONORS

Harry Hayden Academic excellence awardee (2003)

Regina Beck Academic Scholarship winner, Hood College (2005)

Dean’s List Hood College (2006)

MEMBERSHIPS/PROFESSIONAL ASSOCIATIONS

Member of Tri Beta, Biology Honor Society

American Public health Association (APHA)

SELECETED PUBLICATIONS

Emmanuel O. Noumbissie., Pharmacovigilance websites as a preventive tool for drug adverse experiences among the elderly. School of Health Sciences, Walden University. December 2010. (In progress)

Emmanuel O. Noumbissie., Dana G. Cable., Dementia, Ethical challenges of patient treatment and care. Psychology and Thanatology department, Hood College. Spring 2005.

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