CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "Case Report Forms"

Administrative Assistant/Secretary

Coordinated daily activities and provided all areas of administrative support to department supervisor. Scheduled appointments, coordinated and arranged meetings, prepared agendas, reserved and prepared facilities. Ordered and maintained adequate departmental supplies for administrative support and faculty personnel ensuring conformance with the departmental budget, also handled student records

Senior/Lead Clinical Research Associate

Seasoned Clinical Research Professional with 10+ years experience in Clinical Research, including, CRA, Lead CRA, and Project Management duties. THerapeutic areas include oncology, endocrine/metabolism, and CNS.

Ideal Companies: biotech, pharma

Tags for this Online Resume: clinical trials manager, oncology, clinical research

Senior Certified Clinical Research Professional; Oncology Specialist; 15 yrs experience

Senior Clinical Research Professional seeks in-house position within the Pharmaceutical industry working on Phase I-III oncology trials in the Southern NJ or Philadelphia area.

Tags for this Online Resume: clinical research , detail-oriented, quality assurance quality control auditor, oncology, electronic case report form specialist

Medical Statistician-15 years experience-Gloucester Health Authority, Dept of Environment,

My objective is to support all health professionals in understand clinical research from the correct methodology to data collection to data analysis. Can support in writing case report form, questionnaire design,inform consent form

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

Experienced Data Coordinator Relocating to Dallas, Texas

I am looking for a company where I can add to my extensive list of Data Coordinator skills as well as share my skills with others. Working for a company which fosters the expansion of knowledge, is constantly growing and supports its employees is very important to me.

Tags for this Online Resume: SAS, eDM, Oracle Clinical, DMP Composition, CRF Completion Guidelines Composition, External Data Reconciliation, Multi-tasker

Dynamic Administrator

Administrative Assistant with over six years experience in all aspects of corporate communications, time management and client / customer relations who thrives in fast-paced environments. My upper intermediate to advanced proficiency with the Microsoft Office Suite of software gives me the edge in producing superior results and meeting deadlines ahead of schedule. Working in team environments and taking ownership of indiv...

Ideal Companies: IBM, Apple, Ovation Research Grp

Tags for this Online Resume: Administrative Support, Administrative Assistant

Sr. CRA/Clinical Trial Manager

I am seeking full-time or contract position with a mid size biotech or pharmaceutical company. I have 14 years of experience in the industry. The positions/duties include Sr. CRA, Trial Managment, GCP Audits, Site Training on several EDC systems, team generation/review of SOPs, Protocols and Case Report Forms.

Efficient working machine with integrity

Adaptable to any working position in a variety of environments. I am a hard worker and I learn quickly. Capable of working independently and under stress, although I prefer to maintain my work load so as to not have unnecessary stress.

Ideal Companies: Company name is not as important as company style. I desire a company that can compensate me for the energy I put in for their success.

Tags for this Online Resume: Data Entry, Administrative Assistant, Executive Assistant, Sales, Customer Service, New Accounts, Sales Associate