CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "CRF"

Project Management

Multitasking, Problem solving, Leadership.

Ideal Companies: Merck, Wyeth, AstraZeneca, Abbott

Tags for this Online Resume: clinical Trial, data entry specialists, Pharmaceutical Technician

Clinical Research

I have completed a Masters program in Biotechnology. I have keen interest in Clinical Research and Regulatory Affairs. I am looking for an entry level Clinical or Regulatory position. I have research site coordination experience in the areas of Rheumatology and Pain research. I am also ICH and GCP certified.

Tags for this Online Resume: CRF writing, patient follow up, administering informed consent form, administering psycometric scales, source documents review, Reporting SAE’s, Pre-screening and recruiting patients, -Submitted documents to the Ethics Committee, Rheumatology, Pain

Senior Clinical Data Manager

Over 15 years of broad knowledge and experience in clinical database and project management activities in Roche pharmaceutical company. A result-oriented professional who effectively meet project commitment with strong interpersonal communications and ability to interface well with all level of organization. Mentors and support members of study management group. Highly skilled in EDC (Rave) and Oracle clinical data manageme...

Tags for this Online Resume: Medidata Rave, Oracle Clinical, Hyperion, Spotfire, Excel, Word

SAS Programmer Analyst

I strive hard to be the best SAS Programmer in the industry using my advanced skill set in SAS and applying my experiences.

Tags for this Online Resume: SAS, CDISC, CRF, eCTD, FDA, SQL

Clinical Data Manager

Implemented knowledge of ICH GCP and CDISC Standards. Proven organizational skills with the ability to learn quickly; excellent time management, meet tight deadlines; manage multiple tasks and changing priorities while working in a high-pressured environment. Reputable for my attention to detail skills and strong ability to respond and solve problems in real time to fulfill customer expectations. Ability to work effectively...

Tags for this Online Resume: organized, data, bilingual, pharmaceutical, SQL Language, SAS, ClinTrial, ClinAccess, detail oriented

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

Clinical Database Manager

Seek opportunity to work with clinical data in a research setting.

Ideal Companies: The CDC, Johnson & Johnson, Novartis, SAS Institute, Chiron, The Nature Conservancy, National Wildlife Federation

Tags for this Online Resume: database, clinical data, SAS, Microsoft Access, Microsoft SQL Server, Foxpro

Sr. Clinical research Associate/ Director of clinical research

Can undertake most of the tasks and works independently. Very much focussed on the timelines and quite goal tending. Willing to help others in their prioritized tasks. Excellent planning, design and implementation. Highly experienced in writing reports and data analyses.

Ideal Companies: Pharmaceutical industries, Biotech companies, Research institutes, hospitals and for profit mid to large companies.

Tags for this Online Resume: Director of clinical research, Manager of drug safety, Senior clinical research associate, Regional clinical research associate

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

Senior Clinical Research Associate

My objective is ro expand my knowledge of 11 years in clinical research to other avenues of clinical reporting such as data collection and review auditing and CRF data. It all interrealtes to my present experiences.

I use the three R's (Respect for myself, Respect for others, Responsability for my actions) to guide me thru my life and to help me be the best I can be no matter what I do.

I am looking for a job where I can not only expand my mind but, have fun as well(People tend to be better at what they like doing). I would like for my future job to be not just a paycheck but a learning experience and enjoy going to work with every day that comes.

Ideal Companies: Dow Coring, I enjoy working at Manufacturing plants, Sony, Anywhere where I can expand my mind.

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