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Clinical Research Management

Location:
Congers, NY, 10920
Posted:
December 04, 2017

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Resume:

Patrycja Wojtowicz

** **** *********, *******, ** 10920 ac3la0@r.postjobfree.com 302-***-****

QUALIFICATIONS SUMMARY:

Self-motivated, result-oriented professional with continual experience in clinical research. Highly skilled in problem solving and communicating effectively with people at all levels of the organization. Demonstrated excellent managerial, coordination and interpersonal skills. Proven ability to organize, prioritize, meet deadlines, work under pressure and heavy work load. EXPERIENCE:

AMA Laboratories, Inc., New City, NY, USA

2014 – Present

Associate Director of Clinical Studies

Ensuring clinical studies are met and completed according to protocol, project budget, regulatory requirements, GCP, company SOPs and other standards.

Managing internal clinical operations while providing support for logistical and tactical activities related to study conduct.

Preparing essential study documents.

Communicating with clients and maintaining customer satisfaction. 2007 – 2014

Clinical Studies Manager

Designing, conducting and monitoring various clinical studies including Anti-Aging, Wrinkle Reduction, Viscoelasticity by Suction, Antiperspirant Efficacy, Moisture Retention by Electroconductivity, Transepidermal Waterloss (TEWL), Sebum on the Skin Surface, Facial Discomfort Assay, Ophthalmologist Test, Cellulite Reduction, Hair Regrowth, Dandruff Reduction and other Product Claim Substantiation Tests.

Evaluating results of tested cosmetics, collecting and ensuring the quality and integrity of data, preparing and reviewing written reports.

2007 – 2010

Quality Assurance/Quality Control Supervisor

Monitoring and auditing various clinical trials to assure that the conduct, data reported, calculations, personnel involved, equipment, calibrations, and record keeping are in compliance with Federal Guidelines, Protocols and Standard Operating Procedures. EDUCATION:

Kriger Research Center, Inc., USA

2006 – 2007

Clinical Research Associate Professional Development Program

Pharmacology for Clinical Research Professionals. Extensive training in ICH GCP, Clinical Site Monitoring (site selection, initiation, monitoring and close out) and Adverse Events. Silesian University of Technology, Gliwice, Poland 2000 – 2005

Masters of Science in Chemistry - GPA: 4.5 on scale of 5.0 - ranked top 15% of graduating class and awarded University Scholarship for excellent academic performance.

Concentration in Management and Production Engineering.

Completed courses in Organic Chemistry, Biochemistry and Biotechnology, Patent Protection, Drugs and Pesticides, Synthesis of Biological Active Compounds, Chemical Safety, Quality Management, Technology Management, and Chemical Production Management.

TECHNICAL KNOWLEDGE/ SKILLS/ PROFESSIONAL ASSOCIATIONS:

Advanced knowledge of MS Office and Web Research.

Languages include Polish (native), English (fluent written and spoken), Tibetan (read)

Extensive knowledge of scientific devices utilized for measurement of biophysical parameters include Visioscan, Cutometer, NOVA Dermal Phase Meter, Evaporimeter, Corneometer, Minolta Chromameter, Glossymeter and Sebumeter.

Excellent analytical, communication and planning skills.

Demonstrated ability to work independently and as a positive team member.

Member of the Society of Cosmetic Chemists.

VOLUNTEER EXPERIENCE:

Yoga Synthesis, Ramsey, New Jersey, USA

2016 – Present

Community Yoga Class Teacher

United Hospice of Rockland, New City, NY, USA

2012 – Present

Direct Care Volunteer

Providing companionship as well as emotional and practical support to patients and their families.

References available upon request



Contact this candidate