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Coordinator Medical Assistant

Location:
United States
Posted:
September 10, 2014

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Resume:

CURRICULUM VITAE

Robin D. Bowman, BS, CMA (AAMA)

**** **** **** *****

Jamestown, NC 27282

336-***-****

********@*******.***

EDUCATION YEARS DEGREE/DIPLOMA

Appalachian State University 2009-2013 Bachelor of

Science

Boone, North Carolina Psychology,

Sociology

Wilkes Community College 2007-2009 Associate of Arts

Wilkesboro, North Carolina

Wilkes Community College 2002- 2004

Associate of Applied

Wilkesboro, North Carolina Science, Medical

Assistant

Certification: Medical Assistant North Carolina March 2014-

Present #2385923

May 2004-March 2007

EXPERIENCE YEARS LOCATION

PharmQuest 2013-Present Greensboro, North

Carolina

Research Coordinator

Mountain Top Clinical Research 2003-2007 Sparta, North

Carolina

Research Coordinator

SHARE Clinic 2004-2006 Sparta, North Carolina

Certified Medical Assistant

JOB DUTIES / ROLES

. Maintains submission of regulatory documents to sponsors for IRB

approval.

. Performs responsibilities with minimal support from management.

. Implements proper informed consent procedures, compliance with

protocol, GCP/ICH Guidelines and other applicable regulatory

requirements, and assurance of good site performance.

. Performs detailed review of subject records, essential documents,

investigational product disposition and accountability, site personnel

and procedures.

. Performs safety reporting of AEs and SAEs immediately to PI and

Sponsor.

. Maintains prompt attention of data entry, data locks and resolving

queries in a timely fashion.

. Reports all significant issues to appropriate personnel immediately.

. Participates in company-required training programs.

. Performs necessary functions (e.g., creation of source documents,

processing and shipment of labs, and performing ECGs per protocol

requirements).

. Maintains office (e.g., properly securing medical records and

Regulatory Binders).

. Performs other duties as assigned

SOFTWARE EXPERIENCE

. InForm 4.5, 5.5

. Cenduit

. WriteResult

. eTarget

. MyTrails

. ePresentOnline

. ClinTrak

. eClinical OS

. ERT

. iMedidata

. ACE

. Microsoft Office

CLINICAL RESEARCH

Coordinator, "A Multicenter, Randomized, Double-Blind, Placebo-Controlled,

Phase 3 Trial to Evaluate the Efficacy and Safety of BMS-XXXX) as

Monotherapy in Subjects with Type 2 Diabetes Who Have Inadequate Glycemic

Control with Diet and Exercise" (Bristol Myers Squibb - Phase III)

Coordinator, "A Multicenter, Randomized, Double-Blind, Placebo Controlled,

Phase 3 Trial to Evaluate the Efficacy and Safety of (BMS-XXXX) In

Combination with Thiazolidinedione Therapy in Subjects with Type 2 Diabetes

Who Have Inadequate Glycemic Control on Thiazolidinedione Therapy Alone"

(Bristol Myers Squibb - Phase III)

Coordinator, "A Multicenter, Randomized, Double-Blind, Placebo-Controlled,

Phase 3 Trial to Evaluate the Efficacy and Safety of (BMS-XXXX) in

Combination with Metformin in Subjects with Type 2 Diabetes Who Have

Inadequate Glycemic Control on Metformin Alone" (Bristol Myers Squibb -

Phase III)

Coordinator, "A Randomized, Double-Blind, Parallel Group, Multicenter Study

to Evaluate the Efficacy and Safety of ETC-XXXX, and the Combination

in Hypercholesterolemic Patients With or Without Statin Toleranc" (Esperion

- Phase II)

Coordinator, "Pharmacokinetic Evaluations of following Subcutaneous

Administration Using Prefilled Syringe or Auto-Injector in Patients with

Moderate-to-Severe Plaque Psoriasis" - (Lilly - Phase III)

Coordinator, "A Comparsion of versus Human Insulin NPH as Basal

Insulin Treatment in Insulin-Naive Patients with Type 2 Diabetes Mellitus

not Adequately Controlled with 2 or more Oral Antihyperglycemic

Medications: An Open-Label, Randomized Study" (Lilly - Phase IIIa)

Coordinator, "Double blind and Open Label 2 year extension of subq in

prefilled syringes assessing long term safety, tolerability & efficacy in

subjects with moderate to severe chronic plaque-type psoriasis treated with

either a fixed dose regimen or on a retreatment at start of relapse

regimen" (Novartis - Phase III)

Coordinator, "A Multicenter, Randomized, Double-Blind, Double-Dummy,

Placebo-Controlled, Parallel Group, Multi-dose Study Comparing the Efficacy

and Safety of Subcutaneous with Placebo for the Preventive Treatment

of Chronic Migraine" (Labry's - Phase IIa)

Coordinator, "A phase lll, randomized, open-label, active-controlled,

multicenter trial to study the contraceptive efficacy & safety of the

commercial batch of oral tablets of MK-XXXX (nomegestrol acetate-17B-

estradiol) in healthy, sexually-active women aged 18-50 years" (Merck -

Phase III)

Coordinator, "A 4-week, Randomized, Placebo-Controlled, Double Blind,

Efficacy and Safety Study of in Adults with Primary

Hypercholesterolemia" (Zhejiang Hisun - Phase IIa)

Coordinator, "A Multicenter, Randomized, Double-Blind, Placebo-Controlled,

Parallel-Group, Study Comparing the Efficacy and Safety of Two Doses of

Subcutaneous with Placebo for the Preventive Treatment of High

Frequency Episodic Migraine" (Labry's - Phase IIa)

Coordinator, "A Phase 3, Randomized, Double-blind, Active Controlled,

Multicenter Trial to Evaluate the Safety and Efficacy of Compared to

Pioglitazone in Subjects With Type 2 Diabetes Who Have Inadequate Glycemic

Control" (Bristol Myers Squibb - Phase III)

Coordinator, "A Phase 3, Randomized, Three-Arm, Double-blind, Active

Controlled, Parallel Group, Multicenter Trial to Evaluate the Safety and

Efficacy of in Combination With Metformin Compared to Glimepiride in

Combination With Metformin in Subjects Wtih Type 2 Diabetes Who Have

Inadequate Glycemic Control on Metformin Therapy Alone" (Bristol Myers

Squibb - Phase III)

Coordinator, "Multicenter Assessment of Transdermal Therapy in Overactive

Bladder With TDS (XXXX)" (Watson - Phase IV)

Coordinator, "A Multicenter, Randomized, Double-Blind, Placebo-Controlled,

Phase III Trial to Evaluate the Efficacy and Safety of in Combination

With Metformin in Subjects With Type 2 Diabetes Who Have Inadequate

Glycemic Control on Metformin Alone" (Bristol Myers Squibb - Phase III)

Coordinator, "A Multicenter, Randomized, Double-Blind Placebo-Controlled

Phase 3 Trial to Evaluate the Efficacy and Safety of in Combination

With Glyburide in Subjects With Type 2 Diabetes Who Have Inadequate

Glycemic Control With Glyburide Alone" (Bristol Myers Squibb - Phase III)

Coordinator, "A Single-center,Double-blind,Randomised,Placebo-

controlled,Parallel-group Study to Assess the Effect of 24 Weeks of

Treatment With V on Insulin Sensitivity and Its Underlying Mechanism

in Patients With T2DM Treated With Metformin" (Novartis - Phase III)

Coordinator, "A Phase 2, Double-Blind Randomized, Placebo-Controlled,

Parallel Group, Multicenter Study to Evaluate Treatment With in

Subjects With Type 2 Diabetes" (Takeda - Phase II)

Coordinator, "A Phase 3 Double-Blind, Randomized, Placebo-Controlled Study

to Determine the Efficacy, Safety, and Tolerability of in the

Treatment of Subjects With Type 2 Diabetes" (Takeda - Phase III)

Coordinator, "A Phase 2, Double-Blind, Randomized, Placebo-Controlled,

Parallel-Group, Multicenter Study to Evaluate Treatment With in

Subjects With Type 2 Diabetes" (Takeda - Phase II)

Coordinator, "A Phase 2b, Randomized, Double-Blind, Placebo-Controlled

Study of in Patients with Episodic Migraine" (Lilly - Phase 2b)

Coordinator, "A Phase 4, Randomized, Double-Blind Trial to Evaluate the

Immunogenicity and Safety of a XX Pneumococcal Vaccine When

Administered Concomitantly With Seasonal Inactivated Influenza Vaccine in

Adults 50 Years and Older Who Received 1 or More Doses OF 23-VALENT

Pneumococcal Polysaccharide Vaccine Prior to Study Enrollment" (Pfizer -

Phase IV)



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