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Online Resumes with "gcp"
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.
Interested in a management position within the scientific or mechanical segments of the biotech/pharma industry, utilizing my technical and development strengths, expanding my areas of expertise and increasing the scope of my responsibility within a world-class organization.
Senior scientist/clinical supply coordinator with broad experience managing and coordinating pharmaceutical clinical supply systems for API’s, Excipients, Packaging components, Finished drug products including Controlled substances, Reserve samples, and Chemical archives. Labeling and distribution of GMP Clinical supplies for worldwide GLP and GCP studies. Reconciliation and disposition of returned clinical supplies. Pro...
Clinical Supply Operation, Edison, NJ - 8+ Years of experience in pharmaceutical R&D, Clinical supply operations. Knowledge and experience in GMP, GCP and FDA/ICH guidelines. Good experience of computer programming and use of MS Suite of Applications, Dat
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
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.
I wish to secure a position with an organization which allows professional growth, team and individual achievements while purposefully utilizing my qualifications and advancement, and offering opportunities to integrate personal enrichment with professional goals and delivering my best.
Tags for this Online Resume: Research, Scienctist, Manager, Biology, Laboratory, Protocol, Regulatory, Training, Development, Biochemical Assays, Organization, Computer, Colony Breeding, Proficient, Trouble Shooting, Communication, Team, Prioritizing, Goal Setting, Testing, Analysis, Experienced, Leadership, Professional, Reports, GLP, GCP, Scheduling, Patients, Medical, Validation, Environmental Health and Safety, Record Keeping
RAFAEL GOMEZ GAITAN, MD, CRA 5956 S. ZANTE WAY AURORA, CO 80015 PHONE 303-507-8959 E-MAIL: RAFAEL_G_GAITAN@YAHOO.COM To Whom It May Concern: I am seeking a position that will allow my skills in clinical research and medical training to support, as a Clinical Research Coordinator, a medical facility in the treatment of patients or research activi...
Ideal Companies: Clinical Research
Tags for this Online Resume: Clinical
I am looking for a career in the clnical research industry in Clinical Operations: clinical study coordinator, regulatory affairs, project management, etc.
Working currently as Senior CRA and Business Development Manager in UK. Want to relocate to US to be closer to my family. Great knowledge in Scandinavian and European authorities such as MHRA,MREC and R&D.
I WANT TO MAKE A CHALLENGE OF MY POSITION AND EXPLORE MY SKILL TO THE INDUSTRY.
Tags for this Online Resume: Knowledge of biotechnology tool and technique., clinica data management,gcp guideline, knowledge about media preparation for tissue culture., expert in plant tissue culture., knowledge about Recombinant DNA Technology, basic knowledge about PCR AND ELECTROPHORESIS OPERATION
I am seeking a position as a Clinical Research Associate with a Clnical Research Organization. My extensive research and clinical background have prepared me for success in this position.