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Online Resumes with "protocols "



Clinical Quality Assurance - 17 Years of Experience - Near 27713

QUALIFICATIONS: QA / Quality Oversight, Data Integrity, Investigations, six sigma, CAPAs, TrackWise, Root Cause Analysis (RCA), Technical / Collaborative / Creative Writing, Microsoft Office, Inhalation, Stability, HPLC, Analytical Analysis, Quality Control (QC), Quality Assurance (QA), Audits, cGMP, cGLP, GxP, cGCP, method development/validation, Instrumentation/Automation, software, 21 CFR Part 11, FDA / ISO / Internation...

Tags for this Online Resume: Quality, Investigations, Regulatory, Writer, Raleigh, Data Review, Biotech, Test, Atlas, Automation, Data Entry, Documentation, Manufacturing, Protocol, Quality Assurance

Clinical Research - 17 Years of Experience

Clinical Research professional 10+ years experience Strong research interest in program development and operational management. Experience includes coordination and advocacy data interpretation problem solving queries oral/written reports research monitoring assessments and site visits. Demonstrated strong organizational documentation multi- tasking skills in daily practice. Excellent communication analytical and relationsh...

Tags for this Online Resume: Billing, Child Care, Scheduling, Management, Assessments, Clinical Research, Protocol, Research, Distribution, Email

Bookkeeper - 6 Years of Experience - Near 27028

Summary Energetic Administrative Professional with 14 years experience in high-level executive support roles. Organized and professional, adept at managing multiple projects with ease using expert time management methods. Accomplishments General Ledger Accounts Maintained accurate accounts including cash, inventory, prepaid, fixed assets, accounts payable, accrued expenses and line of credit transactions. Customer Service H...

Tags for this Online Resume: Inventory, Inventory management, Management, Accounts Payable, Receivables, Research, Support, Time Management, Complaints, Customer Service

Clinical Research - 20 Years of Experience - Near 07081

Vaud. L'Hôpital Cantonal de Fribourg Performed and led all start-up aspects for a Phase II multi-center study for Crohn's disease. Monitored 120 patients using a PAF antagonist for asthma, including pre-study visits, site initiations, monitoring, and close down. Wrote protocol and designed CRF for a methacholine challenge study. Monitored pharmacokinetic Phase I studies co-wrote final study report.

Tags for this Online Resume: Clinical Research, Research, C Programming Language, Consulting, Hepatitis, Hepatitis C, Pharmaceutical, Protocol, Filing, Health Insurance Portability And Accountability Act

Customer Service Representative - 15 Years of Experience - Near 01545

SUMMARY Talented Customer Service Associate skilled at balancing customer needs and company demands, Effectively builds loyalty and long - term relationships with customers while achieving all individual sales goods. 85% conversion rate, and skilled in exceeding sales goals and company expectations by expending client base and maintaining high standards of customer service. Personable and deadline-drive Customer Service Rep...

Tags for this Online Resume: Housekeeping, Clubs, Complaints, Customer Service, English Language, Fast-paced Environment, GE, Health Care Industry, Insurance, Insurance Sales, New York City, Massachusetts

Supply Chain Manager - 18 Years of Experience - Near 23401

Johnson is a dynamic logistics Intel field operative with experience in documentation, contract logging, supply chain and fleet management, a google rising star in gmail product forum, HoS, google map, and Youtube. Believes in the smart use of e-logistics and internet engine to transactions and trading. He's married with children and ever ready to experience new trends in the industry.

Tags for this Online Resume: Documentation, Logistics, Management, Protocol, Business Development, Business Development Manager, ISO, Audit, Cash receipt, Consulting

Clinical Research - 2 Years of Experience

SUMMARY OF EXPERIENCE Over 3 years of experience of clinical research experience with a clinical research organization. Established a reliable consultants building relationships with a strong commitment to quality. Team oriented, strong organizational skills with attention to detail Phase I-IV Experience. Ability to perform SWAT, PSSVs, SIVs, IMVs, and COVs according to company timeline and deadline. THERAPEAUTIC AREA OF EX...

Tags for this Online Resume: Management, Protocol, Clinical Research, Documentation, Research, Cardiology, Corrective Actions, Data Analysis

Clinical Psychology

Provision Psychology Intern UMDNJ-Robert Wood Johnson Medical Center. of outpatient individual group and couples psychotherapy to geriatric population people with sexual/marital difficulties and general adult outpatient mental health population. - Conducted assessment and differential diagnosis of dementia as part of multidisciplinary treatment team. - Extensive experience providing psychological assessment/testing to outpa...

Tags for this Online Resume: Data General Nova, Facilitator, Support, Gastrointestinal, Gastroenterology, Services, Clinical Research, Protocol

Clinical Research - 8 Years of Experience

To excel further in the field of regulatory affairs and medical writing by leveraging my 8+ years of core experience in this area. To grow with the company by sheer perseverance and by contributing to the success of my team and the organization that I work for.

Tags for this Online Resume: Medical, Regulatory Affairs, Research, Protocol, Clinical Research, Dermatology, Leadership, Lotus

Software Engineer, New York, NY

PROGRAMMER ANALYST Progressive experience in design, coding, testing, implementation of applications (stand-alone and client/server) using various software tools. Hardware: PC, IBM Mainframe Operating Systems: MS Windows XP/9x/2000/NT 4.0, UNIX, DOS 7.0, VM, TSO, CICS, JCL, VAX Alpha/VMS, DOS/Windows Software: C++, VC++, MS Visual Basic, MS SQL, JavaScript, Oracle 10g,11g, Crystal Reports, PeopleSoft 7.0,SQRW, PeopleCode...

Tags for this Online Resume: C++, Oracle 10g, 11g, SQL, PeopleSoft, JavaScript, Testing

Clinical Research Associate - 5+ Years of Experience

Experienced with key clinical trial systems including CTMS, EDC, IVRS and eTMF systems,Recist1.0,ECOG,statistical concept

Ideal Companies: Roche, Pharm-Olam

Tags for this Online Resume: Clinical Research, Compliance, Documentation, Research, Good Clinical Practices, Management, Oncology, Protocol, Cardiovascular, Data Management, CTMS, EDC, SAE reporting