CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "Study documents"

Director of Diversity Initiatives

conference planning and web site experience. Highly organized, with the ability to manage multiple projects and professional staff, and to meet deadlines. Demonstrated experience in workshop development, teaching, and diversity training. Strong work ethic in tandem with a commitment to excellence in all projects undertaken. A team player but with the ability to work independently to accomplish objectives. Strong communicati...

Ideal Companies: Microsoft, Google, Northwestern University, University of Chicago

Tags for this Online Resume: higher education, administration, assessment, diversity, LGBT, survey design, faculty development

Associate researcher in the lab at a Midwestern University studying and documenting summers field research

Experienced Research Professional seeks CRA position!

Passionate, hard-working, intelligent, leader, compassionate, organized

Ideal Companies: I would enjoy working with any CRO or Sponsor who values and rewards excellence and a strong work ethic from their employees.

Tags for this Online Resume: Clinical Research Associate, CRA, Regulatory, Monitor, Auditor, GCPs

CTA

Seeking for a challenging career in a progressive organization offering the opportunity for contributing my skills services to the organization and personal growth and to work sincerely with maximum effort using best talents and with a challenge to achieve required goals and targets, abiding to the decisions of seniors and to earn a good reputation what ever required.

Tags for this Online Resume:  Develop, maintain and manage appropriate study documentation,  Developing, writing and presenting the clinical trial protocols,  Initiate, maintain and reconcile Trial Master File.,  Monitoring the trial throughout its duration which will involve visiting the Study centers on a regular basis to check the patient data in the case report forms (CRFs) and to sort out any problems which may arise.,  Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other Data collection tools by careful source document review Monitor data for missing of implausible data.,  Complete Serious Adverse Event (SAE) reporting, process production of Reports, narratives and follow up of SAEs and managing the clinical data intermilitently as per 21CFR USFDA guidelines,  Monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP and ICH Guidelines.,  Independently perform CRF review; query generation and resolution against established data review guidelines on client data management systems as assigned Perform other duties as assigned by management., , maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned

I am MD by background with more than 5 years of clinical research experience

I am looking for a challenging job in a team-oriented environment.

Ideal Companies: Allergan, Genentech, Ista, Santen

medical device R & D Technician

Excellent hand-eye coordination. Micro component assembly (soldering, epoxy and adhesive bonding, laminating, welding, microscope work). Able to work from written and verbal instructions. Experience with electronics testing, Instron tensile testing, measurements using laser micrometer, caliper, micrometer, snap gage, and microscope. Advanced skills in NiTi etching, hand deburring, hand sculpturing of small components, a...

Tags for this Online Resume: medical device r & d technician, medical device manufacturing technician

Clinical Data Manager, 7 years experience

I am currently looking for work as a Clinical Data Associate, Data Manager or Data Coordinator. During my 7 years in the biotech industry, I have worked on all aspects of Data Management from the Data Entry process to the creation and implementation of the study documentation to the CRF and Database creation and implementation of Edit checks. I also now have a site perspective since my last experience was working directly w...

Tags for this Online Resume: Data Management, pharmaceutical, clinical research, oncology

Legal Assistant

To obtain an entry-level position in the legal or related field, utilizing my education in paralegal studies, document processing, research, and administrative skills, and ability to work in a fast-paced environment.

Registered Dietitian, Certified Diabetes Educator

High-powered, compassionate, and versatile healthcare professional equipped with more than 20 years of experience in Clinical Research, Diabetes Education, and Program Coordination. Show competency to manage delivery of clinical study protocols, clinical study reports, study agreements, applications, and other study documentation. Demonstrate strong analysis, research, documentation, and advocacy expertise, coupled with eff...

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 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...