CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "Clinical Trials "

Ph.D. with Clinical Trial experience

A challenging position, with salary commensurate with the job responsibilities and my education & experience.

Tags for this Online Resume: project management, data cleaning, data workflow, good clinical practices, data management, clinical trial, database, oracle clinical, medical sciene liaison

Resourceful no matter what the task

Independent, organized, and willing to take on a challenge.

Ideal Companies: Academic Universities, Technology Transfer Organizations, Law firm concentrating on contracts

Tags for this Online Resume: technology transfer, license, contract negotiation

Clinical Research Program Manager, Social and Clinical Research, Research Coordinator, Regulatory

Tags for this Online Resume: Regulatory and Compliance, Research Program Manager, Senior Clinical Research Coordinator, Clinical Trials Manager, Research Associate, Research Recruiter

Biostatistician , Stanford

A highly experienced Biostatistician with more than 8 years of training in statistical methodologies and applications, more than 7 years of working experience in medical studies and/or clinical trials

Tags for this Online Resume: Statistician, Biostatistician, Statical analyst, SAS programmer

Mult-talented hard working Contract Manager

Tenacious, high intelligent, very professional, and personable, Contract Manager, looking for an opportunity to step into Contracts Management position with an eye towards Corporate Governance.

Ideal Companies: I have no ideal company.

Tags for this Online Resume: Contract negotiations, compliance, legal analysis, contract drafting, corporate governance

Medical Receptionist

Here are my skills,I have worked in clinical trials as Assistant Project Manager,Documentation Control Pharmaceutical,Medical receptionist Doctor(temporary postion) Organization – Document preparation for Federal Government agency Created archives for all documents, per the Food & Drug Administration regulations. I created a more efficient filing system. Excellent attention to detail Team Player- flexible Awa...

Ideal Companies: Medical Assistant Bacic, Medical Assistant Advance

Tags for this Online Resume: attention to detail, Microsoft Word, Customer Service, Lite Data Entry, Phone Etiquette, orgainized

Clinical Supplies Manager

Consistently produced investigational medicinal products within aggressive timelines and according to cGMP guidelines as required by study protocols. Strong Program Management skills with an emphasis on the design and forecasting of accurate drug demands for multiple ongoing global Clinical Trials. Proficient in communicating with a diverse group of people including team members and vendors. Achieved objectives through my ...

Latin America Finance & Accounting Director (Clinical Trials)

Latin America Finance and Accounting Director with solid experience in international and domestic accounting (GAAP), financial analysis, planning, budgeting and forecasting with experience in building, leading and advising in financial and accounting processes in international expansion. Excellent leader with a solid record of contributions leading to improved financial performance, heightened productivity and enhanced int...

Pharmacovigilance physician

I want to be the pharmacovigilance medical head of any reputed pharma company

Tags for this Online Resume: drug safety, pharmacovigilance, medical monitor, medical safety, clinical trials, risk-benefit

DR.

Medical Doctor - 20years experience - Pediatrician Medical care /Research- Salary Chief Medical Officer - State Goverment Research in field of Malaria, Nutrtion and HIV National Facilitator in field of Malaria,Nutrition and HIV Member: Malaria Clinical Trial Alliances (MCTA)/INDEPTH

Tags for this Online Resume: Medical Doctor/Reseacher

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

Research Coordinator - Ft. Worth, Texas

Would like to continue working in the Research area. It gives me great pleasure to help patients.

Tags for this Online Resume: Research Coordinator, Clinical Trials, IRB