Jodean A. Campbell,

B.Sc., M.Sc.

Summary

I have a strong background in the basic sciences (B.Sc. Biology), Clinical Research (M.Sc. Clinical Research Administration) with experience working as a Clinical Research Coordinator and Patient Educator (recruitment), & the Medical Sciences (Basic Science Certificate, towards M.D.)

Skills & Abilities

Data Analysis, Power BI, SAS, Tableau, Python, mySQL, SQL Query, Access, Excel, Agile SCRUM, Pharmacovigilance, Subject Recruitment, EDC, IQVIA, Study Teams, Veeva, ARGUS, Behavior Analysis, Physical/Psychological Management Training (PMT), Education, Anthropometry, Standardized Interviews, Clinical Operations, Clinical monitoring/management plan,, vendor-specific, Investigator Site File (ISF), Safety management plan and SAE, Interactive Response Technology (IRT), Trial Master File (TMF), TMF management plan, FTEs, Clinical Laboratory.

Experience

SUBSTITUTE TEACHER/SPECIAL EDUCATION/SCIENCE, KELLY EDUCATION

FEB 2023 - PRESENT

Maintains the established routines and procedures of the school and classroom to which assigned. Teaches lesson plan(s) as outlined by the absent teacher. Creates a classroom environment that is conducive to learning and appropriate to the interests of students. Experienced behavior therapist for neurodivergent. Responsible for self-contained pre k special education classroom and one-on-one instruction for a 7th grade special education student, with focus on applied behavior analysis to establish structure needed to facilitate Instructional Education Plans (IEPs) and Behavior Implementation Plans (BIPs).

PHARMACOVIGILANCE COORDINATOR, PROPHARMA

MAR 2022 – OCT 2022

Processed & reported adverse events into ARGUS Product Safety database for NOVAVAX. Processed other safety related data for third party investigational products and various phase clinical trials. Expertly coded adverse events using standardized medical terminology from a medical coding dictionary, such as MedDRA. Performed quality review of adverse event reports and source documents, ensuring that activities were consistent with SOPs.

PATIENT EDUCATOR, CARE ACCESS

OCT 2020 – FEB 2021

Achieved above average call and subject enrollment rates while managing subject recruitment & retention processes for phase II-III Ely Lilly Covid antibody clinical trials. Administered Informed consent. Prepared & uploaded IFCs to IQVIA’s EDC/eCRF. Liaised with CRC’s and other project staff for transition to IP infusion schedule.

FIELD INTERVIEWER, NORC

SEP 2013 – SEP 2014

Maintained a high level of efficiency, having completed the most subject interviews in the region for NIH sponsored National Children's Study schedule. Maintained professional relationship with subjects for retention purposes. Performed and documented anthropometric measurements. Collected and shipped bio/environmental samples.

LABORATORY TECHNICIAN, UNILEVER OCT 2010 – OCT 2011

Supported laboratory staff by maintaining glassware, logs, and record books; inventory control, troubleshooting and resolving problems and helping with special projects. Prepared and stored small batches per strict formulation recipe. Practice Good Manufacturing Procedures (GMP) by documenting information by maintaining daily logs and equipment record books. Optimized bench workflow by organizing and implementing streamlined processes.

CLINICAL RESEARCH COORDINATOR MAR 2010 – OCT 2010

Managed five Alzheimer’s disease phase 3 clinical trials. Responsible for protocol adherence for all aspects of the study, including subject enrollment/retention, source document/EDC records, order inventory, investigational product administration, regulatory binder maintenance, coordination of appointments.

Education

DEC 2021 - PRESENT

CERTIFICATE DATA ANALYSIS, COMPUTER TRAINING SOURCE

Currently pursuing various data visualization/programming certifications (SAS, Agile Professional, Microsoft Certified Data Analyst (Power BI/Access), Tableau, SQL, Python).

AUG 2021 – DEC 2021

CERTIFICATE CLINICAL DATA MANAGEMENT, BCRI INTERNATIONAL

Experience developing eCRFs, writing edit check specifications, developing UAT plans, performing data validation, creating data entry guides and data management plans, start-up CDM activities for new studies in RAVE EDC, performing data review utilizing SAS, managing database lock & reviewing reconciliation reports.

OCT 2016 – SEP 2018

M.SC., CLINICAL RESEARCH ADMINISTRATION, WALDEN UNIVERSITY

Exploratory coursework in product development, the business of clinical research, epidemiology, and good clinical practice.

JAN 2007 – DEC 2009

B.SC. BIOLOGY, THE PENNSYLVANIA STATE UNIVERSITY

Survey of general biology. GPA. 3.01

ad4i1h@r.postjobfree.com ٠ BRIDGEPORT, CT ٠-203-***-****

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