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Skills Summary: • 18+ years of program management experience in global health and clinical research• Excellent cross-cultural communication and interpersonal skills gained through professional experience in the U.S., Africa, Asia and South America• Highly effective working both independently and collaboratively as part of a team• Ability to improvise and manage shifting priorities while coordinating multiple projects2019 - presentEmory University Atlanta, GAProgram Director: Strategic planning and overall program management for human subjects research conducted by Emory University and Albert Einstein College of Medicine investigators• Works closely with a team of 6 Principal Investigators; supervises a Business Manager, Data Manager, Assistant Program Director and 5 Project Coordinators• Support of P30, U19, R01, R21, K awards, pilot studies, and Gates-funded projects aimed at improving prevention, care, and treatment of drug-resistant TB, TB/HIV co-infection, latent TB infection, and the impact of TB on non-communicable diseases such as diabetes. • Budget creation and oversight, staff effort distribution, and contract negotiations with domestic and international sites2014 - 2019Emory University Atlanta, GAProject Coordinator: Oversight of 6 NIH-funded observational studies in South Africa, Kenya, Ethiopia, Brazil, India and U.S., examining outcomes in subjects diagnosed with LTBI, drug-susceptible TB, and drug-resistant TB.2012 - 2014Emory University Atlanta, GA (consultant)Project support for 2 NIH-funded studies on drug-resistant TB in KwaZulu-Natal, South Africa 2012 - 2014ICAP, Columbia UniversityProject Coordinator: 2 implementation science studies seeking to improve TB and HIV treatment adherence in Lesotho and Ethiopia2011-2012Albert Einstein College of Medicine Bronx, NYProject Coordinator: Observational study in KwaZulu-Natal, South Africa2009-2011Columbia University Medical Center New York, NYClinical Coordinator, Department of Dermatology: Phase I through IV studies2008-2009 Rockefeller University New York, NYClinical Research Auditor/Monitor: Phase I through Phase IV studies; multiple areas2006-2007
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Program DirectorEmory UniversityPhiladelphia, Pa, Us -
Program DirectorEmory University Jun 2019 - PresentStrategic planning and overall management of large global health research program, including multiple federally-funded research grants focused on TB and conducted at sites in South Africa, Kenya, Ethiopia, India, Brazil and U.S. Support of 6 investigators and supervision of 10 research staff and 10+ graduate research assistants. -
Research Project SupervisorRollins School Of Public Health At Emory Aug 2014 - May 2019Philadelphia, Pa And Atlanta, Ga -
ConsultantEmory University Jul 2012 - Aug 2014• Providing administrative support and research expertise for two 5-year NIH-funded grants assessing drug-resistant TB outcomes in patients in KwaZulu Natal, South Africa.• Preparing and submitting documentation to ethics committees in U.S. and South Africa including preparing submissions, tracking approvals, editing study documents for amendments and preparing renewal applications.• Developing study documents and preparing submission to the NIH for successful supplemental grant award… Show more • Providing administrative support and research expertise for two 5-year NIH-funded grants assessing drug-resistant TB outcomes in patients in KwaZulu Natal, South Africa.• Preparing and submitting documentation to ethics committees in U.S. and South Africa including preparing submissions, tracking approvals, editing study documents for amendments and preparing renewal applications.• Developing study documents and preparing submission to the NIH for successful supplemental grant award application.• Tracking recruitment and troubleshooting problems with enrollment and retention for supplement grant.• Monitoring storage of lab samples in South Africa, shipment of samples from South Africa to U.S. collaborators, and results of lab tests conducted in U.S.; updating study database with relevant lab information.• Assisting Principal Investigator in reviewing resumes and references, as well as in conducting interviews for three research staff positions at Emory University.• Training newly-hired research coordinators in Atlanta and on-site in South Africa in study management, monitoring of study data, creation of debriefing presentations, and interaction with local study staff.• Following up with Einstein finance department regarding invoice processing and closure of contracts for studies. Show less -
Project CoordinatorIcap At Columbia University Oct 2012 - Jan 2014New York, Ny; Meseru, Lesotho; Dire Dawa And Harari, Ethiopia• Project start-up activities and milestone tracking for two implementation studies addressing high rates of HIV and TB coinfection in African populations: 1) Lesotho: intervention aimed at increasing ART initiation in HIV-infected patients newly diagnosed with tuberculosis 2) Ethiopia: intervention to increase number of HIV-infected patients who initiate Isoniazid preventive therapy (IPT) as prophylaxis to TB infection • Coordination of all ethics submissions to Columbia… Show more • Project start-up activities and milestone tracking for two implementation studies addressing high rates of HIV and TB coinfection in African populations: 1) Lesotho: intervention aimed at increasing ART initiation in HIV-infected patients newly diagnosed with tuberculosis 2) Ethiopia: intervention to increase number of HIV-infected patients who initiate Isoniazid preventive therapy (IPT) as prophylaxis to TB infection • Coordination of all ethics submissions to Columbia IRB, Lesotho National Ethics Research Committee, and Ethiopian National Health Research Ethics Review Committee. Includes initial applications, amendments and annual renewals.• Drafting communication to federal funding agencies (USAID and NIH) in response to funders' queries concerning study status, procurement, and quarterly and annual progress reports.• Acting as primary liaison between New York investigators and study teams in Lesotho and Ethiopia, including tracking enrollment and retention on a weekly basis, developing agendas for weekly conference calls and distributing action items resulting from those calls.• Training and supervising African study teams, especially in-country Study Coordinators. • Monitoring study data collection and in-country study teams' adherence to protocol, GCP and human subjects protections through weekly conference calls and quarterly trips to each country. Show less -
Project Coordinator, Hiv And Tb ResearchAlbert Einstein College Of Medicine Mar 2011 - Oct 2012Bronx, Ny And Durban, South Africa• Responsible for overall project management of NIH research study examining the treatment of HIV-infected patients who also have multi-drug resistant tuberculosis (MDR-TB)• Monitoring study documents and training and supervising study staff located in South Africa• Submitting documents for ongoing review by ethics committees at Einstein, Yale and at research groups in South Africa• Travel 3-4 times a year to research sites in KwaZulu-Natal province of South Africa -
Clinical Coordinator, Dept Of Dermatology Clinical Research UnitColumbia University Medical Center Aug 2009 - Feb 2011• Assisting in all activities involved in clinical trials investigating treatments for skin, hair and nail diseases.• Screening potential research participants and providing informed consent; drawing and processing blood and serum samples for safety analyses; maintaining study binders;dispensing and reconciling study medication; and providing patient education and ensuring subject compliance with protocol.• Responsible for creating and submitting all regulatory documents and IRB… Show more • Assisting in all activities involved in clinical trials investigating treatments for skin, hair and nail diseases.• Screening potential research participants and providing informed consent; drawing and processing blood and serum samples for safety analyses; maintaining study binders;dispensing and reconciling study medication; and providing patient education and ensuring subject compliance with protocol.• Responsible for creating and submitting all regulatory documents and IRB submissions, including IND submissions.• Working with Director, Investigators and other staff members in developing and adhering to study-specific budgets. Show less -
Clinical Research Auditor And MonitorRockefeller University Apr 2008 - Aug 2009• Auditing investigator-initiated clinical trials that include research on vaccines, medications and devices• Organizing and presenting bi-monthly seminars to educate research staff on various GCP topics• Researching and developing community outreach and recruitment opportunities• Providing plain language assistance to Investigators and study staff when developing written materials for study participants -
Clinical Research CoordinatorCri Worldwide Llc Apr 2007 - Nov 2007• Coordinating an average of five studies simultaneously, include projects that dealt with various central nervous system disorders including schizophrenia, bipolar disorder, major depressive disorder and Alzheimer's• Responsible for recruitment, providing informed consent, completion of study visits, drug accountability, electronic data capture• Implementing research studies designed by several pharmaceutical companies, including but not limited to Novartis, AstraZeneca, Pfizer… Show more • Coordinating an average of five studies simultaneously, include projects that dealt with various central nervous system disorders including schizophrenia, bipolar disorder, major depressive disorder and Alzheimer's• Responsible for recruitment, providing informed consent, completion of study visits, drug accountability, electronic data capture• Implementing research studies designed by several pharmaceutical companies, including but not limited to Novartis, AstraZeneca, Pfizer, Acadia, Janssen Show less
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Clinical Research Coordinator IiThomas Jefferson University Jun 2006 - Mar 2007• Responsible for recruitment, informed consent and completion of study visits for treatment of opioid-dependent pregnant women and their newborns• Administering weekly psychosocial assessments and thrice-weekly supervised urine drug screens• Scheduling blood draws and obstetrics appointments, attending ultrasound appointments with study participants• Working with medically responsible investigators to determine dosages for study patients and communicating with Investigational Drug… Show more • Responsible for recruitment, informed consent and completion of study visits for treatment of opioid-dependent pregnant women and their newborns• Administering weekly psychosocial assessments and thrice-weekly supervised urine drug screens• Scheduling blood draws and obstetrics appointments, attending ultrasound appointments with study participants• Working with medically responsible investigators to determine dosages for study patients and communicating with Investigational Drug Service pharmacy staff and the dispensing nurses regarding medication inventories for a narcotic substance Show less
Angie Campbell Skills
Angie Campbell Education Details
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University Of Notre DameAnthropology -
Cultural And Social Anthropology -
Anthropology -
Institute For Shipboard EducationStudy Abroad -
Stanford UniversityCultural And Social Anthropology
Frequently Asked Questions about Angie Campbell
What company does Angie Campbell work for?
Angie Campbell works for Emory University
What is Angie Campbell's role at the current company?
Angie Campbell's current role is Program Director.
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What is Angie Campbell's direct phone number?
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What schools did Angie Campbell attend?
Angie Campbell attended University Of Notre Dame, Stanford University, University Of Notre Dame, Institute For Shipboard Education, Stanford University.
What skills is Angie Campbell known for?
Angie Campbell has skills like Clinical Trials, Clinical Research, Gcp, Protocol, Research, Edc, Irb, Project Management, Ich Gcp, Training.
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Angie Campbell
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