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Online Resumes with "GCP"
Clinical Research Coordinator
To join a clinical research organization as a productive team member and gain career growth while utilizing my in depth clinical research knowledge and experience.
Tags for this Online Resume: Research , Research Coordinator, GCP/ICH and FDA guidelines, Protocols, Phase
Regulatory Affairs - Clinical Research
I am looking to return to the Regulatory Affairs/Institutional Review Board (IRB) arena in Clinical Research. The majority of my research experience is in Human Subjects Research Protections via the IRB/R & D Committee. Although my experience in regulatory affairs is not as extensive, I am looking to connect with Clinical Research Organizations, Pharmaceutical Companies, or Academic Institutions for employment to add to my ...
Tags for this Online Resume: Clinical Research, IRB, Regulatory Affairs
Senior Clinical Research Associate
Continue my service, as an educator and monitor in clinical trials for product development with major pharma/device company.
Tags for this Online Resume: Clinical Research Associate, GCP/ICH Guidelines, Bachelor Degree, Clinical Research Coordinator, ACLS Certification, Registered Nurse
Senior Clinical Research Coordinator
To obtain stable, long-term position in the industry where my experience and skills will be an asset
Ideal Companies: Pharmaceutical, Medical device, Hospital/clinics, Government
Tags for this Online Resume: Senior Clinical Research Coordinator, Clinical Research Monitor-Medical Devices, Study Manager-start up CRO, Regulatory Affairs Specialist, IRB Coordinator/Specialist, Mental Health Counseling-College Graduate, GCP, ICH
"Clinical Research Nurse" "Drug Safety Specialist"
Career Summary Experienced professional nurse with planning and organizational skills of project activities to support investigators in the preparation and conduct of research protocols to ensure compliance in accordance to FDA, GCP and ICH requirements.
Senior Clinical Data Manager with 19 years of experience, Buffalo, NY - remote dm
Seasoned Clinical Data Manager with experience in complex projects and in managing multiple large, international clinical trials for Phases I - IV to GCP/ICH standards in biotech, pharmaceutical and non-profit venues. Ability to work within a complicated matrix environment while also independently self disciplined. Possesses solid project management skills with the ability to anticipate problems relating to projects and to ...
Tags for this Online Resume: EDC Leader, Medidata Rave, InForm, DM/Study Recovery Specialist, Mentor, Trainer
Clinical Research Project Manager-Pharma experienced-MPH-10+ years experience-GCP/ICH/FDA guidelines
Desire capstone experience integrating clinical research expertise, MPH, and medical writing. Would like to utilize adult learning theory in training/coaching role. Excited to apply critical thinking and project management skills to make a difference in patients' well-being.
Admissions Director
Tags for this Online Resume:
public speaker, positive attitude, leader, great manager, GCP, Quality Assurance
Featured Profile
Registered Nurse - Drug Safety Associate,Coder, Product Surveillance/Product Safety
I am seeking for a stable and well established company that is growing. Also,what I am looking for in a new job is for employers that care about their employees and acknowleges them for their good hard work. I would also hope that good training is provided so that the individual such as myself can be productive for the company and contribute towards it's success rate. I would also hope that it was a warm welcoming environm...
Ideal Companies: Cephalon Pharmaceutical, Teva Pharmaceutical, Azur Pharmaceutical, GlaxoSmithKline, United BioSource
Tags for this Online Resume:
Registered Nurse, Drug Safety Associate, Coder, Safety Surveillance, Adverse Event Coordinator
Director of Quality Assurance
Direct quality assurance for biopharma company, quality systems lot release investigations, audits, GLP GCP interface with GMP. Department of 20 -50, with increasing responsibility world-wide.
Tags for this Online Resume:
quality assurance, biopharma, quality systems, lot release, investigations, GLP GCP interface with GMP
Molecular diagnostics, clinical trail associate, clinical trial assistant
I am a professionally trained scientist with 6 years of experience ensuring high standards. I am expert in managing multiple projects simultaneously with excellent communication skills demonstrated by more than 3 years of experience in industry and in academics. Extensive experience managing large‐scale projects from the requirements gathering phase to completion. Ability and interest in learning and incorporating new te...
Tags for this Online Resume:
Molecular diagnosis, molecular biology, clinical research associate, scientist, disease diagnosis, science, PCR, q-PCR, ELISA, Cloning, GCP, Protein purification, Mouse, diabetes, obesity
Registered Nurse - Drug Safety Associate,Coder, Product Surveillance/Product Safety
I am seeking for a stable and well established company that is growing. Also,what I am looking for in a new job is for employers that care about their employees and acknowleges them for their good hard work. I would also hope that good training is provided so that the individual such as myself can be productive for the company and contribute towards it's success rate. I would also hope that it was a warm welcoming environm...
Ideal Companies: Cephalon Pharmaceutical, Teva Pharmaceutical, Azur Pharmaceutical, GlaxoSmithKline, United BioSource
Tags for this Online Resume: Registered Nurse, Drug Safety Associate, Coder, Safety Surveillance, Adverse Event Coordinator
