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Online Resumes with "Phase I IV"



Associate Clinical Project Manager, Raleigh

A career in project management within a clinical research environment that is challenging, yet supportive, enabling me to utilize my core interpersonal & professional skills.

Tags for this Online Resume: oncology, feasibility assessment, phase i-iv, project management

Clinical Research Coordinator, New York City, NY

Accomplished and detail-oriented Clinical Trials Scientist poised to leverage related clinical laboratory/trials and research expertise to excel within the biomedical industry. Demonstrated capacity to work both independently and within teams to achieve project success and facilitate productive discussions and innovative results. Outstanding organizational, interpersonal, and self-motivation abilities; excel in results-orie...

Tags for this Online Resume: Clinical Trials, IRB, Protocol Budget Drafting, Clinical Studies, Phase I-IV

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Senior Biomedical Equipment Technician

To continue career in the field of Biomedical / Clinical equipment technology either in house or in the field.

Tags for this Online Resume: Clinical Engineering, Healthcare, Biomedical Equipment, Technician, Medical Equipment, Maintenance

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Clinical Research Associate

SUMMARY OF QUALIFICATIONS • Foreign graduate Medical Doctor and licensed RN with more than 22 years of clinical and research experience. US citizen. Fluent in English, Russian and Romanian • Extensive training in Good Clinical Practices, ICH Guidelines, SOPs through various Sponsors • In depth therapeutic and protocol knowledge as per Sponsor’s assignment. Excellent organizational and problem-solving skills.

Ideal Companies: Biotech companies

Tags for this Online Resume: research associate, biotech, CRA, Las Vegas, pharmaceutical, health

Senior Clinical Data Manager with 19 years of experience, Buffalo, NY - remote dm

Seasoned Clinical Data Manager with experience in complex projects and in managing multiple large, international clinical trials for Phases I - IV to GCP/ICH standards in biotech, pharmaceutical and non-profit venues. Ability to work within a complicated matrix environment while also independently self disciplined. Possesses solid project management skills with the ability to anticipate problems relating to projects and to ...

Tags for this Online Resume: EDC Leader, Medidata Rave, InForm, DM/Study Recovery Specialist, Mentor, Trainer

Regional Clinical Monitoring, Kansas City, MO

To monitor clinical trials of all phases using extensive knowledge of drug development and regulatory processes. Experience: - study site selection and set up – preparation of pre-study regulatory documentation - preparation of site monitoring reports in accordance with specific timelines - follow-up and resolution of sites issues - identifies and assists sites with DCF resolution - maintains regular contact with ...

Tags for this Online Resume: Clinical Trial Manger, Clinical Research Associate (CRA), Medical Writer (MW), Project Manager, Clinical Research Scientist, Clinical Operation

• In-depth therapeutic and protocol knowledge

To utilize my board medical experience, as a bilingual foreign doctor, in conducting Phase I-IV clinical studies, offering strong project management experience in prioritizing workload and utilizing my knowledge and initiative to drive for results in supporting drug development pipeline goals

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Documentation Specialist

Efficient, accurate and pay close attention to detail

Ideal Companies: Tap Pharmaceutical, Baxter, Hospira, County Clerks Office

Tags for this Online Resume: Administrative Support, Clerical, Records Management, Data Entry

Clinical Research

Tags for this Online Resume: Clinical Research Associate, Monitor, Research Manager, CCRC, CRA, Phase I-IV

Clinical Trials Associate

Michelle Straka, BSHS, CPT 1163 Portsmouth Circle Medina, Ohio 44256 Cellular: (216) 337-2007 Home: (330) 722-2165 Email: dodgestealthrt1994@yahoo.com Linkedin account: http://www.linkedin.com/pub/michelle-straka/1b/964/aa2 Objective Obtain the position of Clinical Research Associate to further advance monitoring career. About four years additional experience in research as a study coordinator, regulatory coordina...