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Online Resumes with "GCP Guidelines"



AS A CLINICAL DATA COORDINATOR

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

Clinical Trial Monitor/Manager - 6.4 yrs experience in Clinical Trial monitoring.management. Therapeutic expertise: Oncology. Others: GI, Resperitory, CVS, Nephrology, Endocrinology.

My Career Objective: To contribute my best of knowledge and skills in the field of Clinical Research to an excelling Pharma/CRO company which conducts quality and ethical clinical trial as per GCP guidelines. Also to bring profit to the company in drug development & pahrmaceutical market by timely delivery of quality work. I also strive to enhance my knowledge and skills and excel in career at all level.

Tags for this Online Resume: Sr. CRA, Clinical Team Lead, CRA, Clinical Trial Assistant, Clinical Project Manager

Master of Pharmacy with 7+ yrs exp

Looking for QC/QA/Clincal research/Formulation/Sales job at entry level.

Ideal Companies: Pharmaceutical, Heallthcare, Clinical research, Pharmaceutical Sales

Tags for this Online Resume: UV, IR, GC, KARL FISCHER, WET CHEMISTRY, ICH GCP GUIDELINES, GMP/ GLP, FORMULATION, QA

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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

Registered Nurse - 25 years experience CRA one year experience

Clinical Research Associate. Also RN with 25 years plus experience. Looking for position with pharmacology or hospital of clinical research.

Tags for this Online Resume: Clinical Research Associate, Registered Nurse, Ability to travel, Ability to work at home, FDA/ICH GCP Guidelines, MS Work knowledge

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Clinical Research Associate, Boston

 To acquire a position as a Clinical Research coordinator in a pharmaceutical company or a CRO that will benefit from my skills, knowledge, experience and enthusiasm and that will give me an opportunity to learn and grow further.  To be responsible for the administration, initiation and monitoring of the Clinical research project in accordance with the FDA regulations and ICH-GCP guidelines.

Tags for this Online Resume: clinical research assistant, data administrator, regulatory affairs assistant, CRA, Drug safety associate, Quality Assurance, clinical research associate

Drug Safety / Pharmacovigilance - RTP, NC

Dynamic, enthusiastic, and performance-driven Doctor of veterinary medicine intent on transferring 10 years of knowledge and experience in a clinical setting to a challenging career working in the Pharmaceutical or Contract Research Organization industry with a progressive company offering opportunities for growth and advancement. Outstanding team player and communicator with highly detailed documentation skills seeking t...

Tags for this Online Resume: Medical terminology, ICH/GCP guidelines, DIsease states, Pharmacology, Customer service, Medical writing

Clinical Research, Raleigh

To Obtain a position congruent with my education and level of experience in the Clinical Research field.

Tags for this Online Resume: Clinical Research Associate, Clinical Research Associate, ICH-GCP Guidelines, ICH-GCP Guidelines, Source Verification, Source Verification, Regulatory Document Maintenance, Regulatory Document Maintenance, Site Initiation Visits, Site Initiation Visits, Drug Accountability, Drug Accountability

Clinical Research 14 years experience

My objective is to use my extensive knowledge of clinical research, FDA, ICH, and GCP guidelines to obtain a career in the Pharmaceutical/Biotech industry.

Tags for this Online Resume: Clinical Reserach, IRB, Human Subject Protection, Audit, Monitor

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.