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Online Resumes with " Clinical Trials Protocol"
MD scientist
Ideal Companies: Any Biotech/Pharmaceutical or Financial company
Senior Business Analyst with Clinical Trials focus
I am a Business Analyst with over 10 years experience in a clinical trials environment. I have excellent requirements gathering and documentation experience as well as experience in testing and training. I am looking for a company in which I can grow and stay. I was with my last company for over 16 years. I would like to remain in the healthcare arena if possible, but am open to other industries.
Ideal Companies: McKesson, Kimberly Clark, Home Depot
Tags for this Online Resume: Functional Specifications, Use Cases, QA Testing, Documentation, Clinical Trials, Laboratory Information Systems
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
Lead Project Manager- Clinical Trials
Proven expertise in managing teams, streamline project paths encompassing an understanding of scientific data, analysis and interpretation of results, clinical developability and commercial viability of projects.
Ideal Companies: Vertex Pharmaceuticals, Amgen Inc., Takeda Pharmaceuticals
Excellent Administrative Coordinator
Detail oriented, independent individual with super interpersonal skills
Ideal Companies: State of Colorado, Federal Government, Local Government
Tags for this Online Resume: Compliance Officer, Manager, Regulatory
An excellent administrator
An excellent program manager with a proven track record of meeting deadlines and shifting priorities as needed. Honesty, integrity and high ethical standards combined with a great sense of humor to "keep it real".
Ideal Companies: State of Colorado, Federal Government, Various Offices in Denver
Tags for this Online Resume: Office Manager, Program Managment, Administrator
Senior healthcare/public policy/governmental analyst; Wilmington, Delaware
I have 22 years of experience in substance abuse and related fields, 13 years of experience as technical editor, and 22 years of experience in analyzing program effectiveness for family and social services, substance abuse, violence prevention, and community development. I also have experience in State- and local-level planning, program, and policy development, State- and local-level strategic plan development and implement...
Tags for this Online Resume: Healthcare analyst, Technical editor, Program and policy analysis, Strategic plan development, State and local level program planning, Federal contracting
Clinical Trial Specialist / CRA _ Home based
Achieve the successful of clinical trial and ensure the subject safety and the high data quality by working closely with each clinical site and ensure that all the tasks are being conducted in accordance with the clinical trial protocol , ICH GCP guidelines and local regulations.
