---

Online Resumes with "Good Clinical practices"

Clinical Research - 14 Years of Experience

Nursing professional with management experience in conducting phase Ib – IV pharmaceutical clinical trials in Cardiovascular, Endocrine, Respiratory, GI, and Immunology diseases. Broad base knowledge of FDA regulations and Good Clinical Practices for study start-up, execution, and completion using applicable SOPs and site policies and procedures

Tags for this Online Resume: Research Nurse Coordinator, Drug Safety Specialist

Quality Assurance Auditor - 12 years Experience - Pharmaceuticals

Quality Assurance Auditor with proficient skills and experiences in various compliance disciplines. Have a passion to conduct local, international, and global audits, training, and provide guidance services within the following regulatory specialties: â?¢Good Laboratory Practices (GLP) 21 CFR Part 58 â?¢Good Clinical Practices (GCP), VICH GL9, Document 85 â?¢Environmental Protection Agency GLP (EPA-GLP), 40 Code of Federa...

Tags for this Online Resume: Auditor, GLP, GCP, Quality Assurance, QA Manager, QA Auditor

Licensed Nurse - 8 Years of Experience - Near 77547

Client focused well regulated, licensed vocational nurse with proven expertise in clinical trials, staff development, client/family education and advocacy, administrative experience, exceptional client care and supervisory roles. Dedicated, accomplished, goal achieving, highly perceptive individual and a respected team leader with a proven ability to lead and motivate team members. A goal oriented individual looking to ad...

Tags for this Online Resume: Clinical Research, Protocol, SOP, Clinical Monitoring, Good Clinical Practices, Clinical Trials, Training/Leadership, Database

Life Scientist - 15 Years of Experience - Near 07080

Accomplished researcher in the field of neuro-/psycho-pharmacology with extensive background in laboratory and project management along with special expertise in laboratory operation, project leadership, personnel training and scientific consulting and negotiation. Interested in pursuing a successful career in research-orientated biotech environment.

Tags for this Online Resume: Leadership, Documentation, Immunoassays, SOPs, Good Laboratory Practices, Bench work, Management, Protocol, Research, Documentation, ELISA, Good Clinical Practices, Good Laboratory Practices, Infrastructure, Management, Protocol, Research, Documentation, ELISA, Good Clinical Practices, Good Laboratory Practices, Infrastructure, Management, Protocol

Clinical Administrative Assistant and Documentation Quality Assurance - 6 Years of Experience - Near 46038

To become a highly contributing member of a healthcare system or corporate setting where I can utilize, sharpen, and expand my professional experience, knowledge, and skills.

Tags for this Online Resume: Document Management, Good Clinical Practices, Proofreading, Research and Development, Protocol, Fishers, Indiana, Strong Organizational Skills, Keen Eye for Detail, Proficient in Word, Excel, and Outlook, Familiarity with Clinical Regulatory Documents, Screening and Recruitment, Investigator Notebook, Dedicated and focused

Clinical Research Coordinator with 9 years experience including phlebotomy, EKG

I aspire to learn new avenues in any job. Learning new things is my passion and attention to detail is a goal of mine in any job.

Tags for this Online Resume: Buffalo, NY CRC, Buffalo NY Medical Assistant, Administrative Skills, Clinical Research, Data Entry, Dialysis, Documentation, Forth Programing Language, Good Clinical Practices, Health Insurance Portability And Accountability Act

Medical Office Manager - 1 Years of Experience - Near 02120

Seeking a position to utilize my skills and abilities in the corporate sector that offers professional growth which is being resourceful, innovative and flexible. Knowledge of ICH guidelines and safety reporting requirements, good manufacturing practices (GMP), good laboratory practice (GLP) and good clinical practices (GCP). Understanding of FDA regulations and knowledge of IND, NDA, BLA, Drug Master File (DMF), 510(k) and...

Tags for this Online Resume: Boston, GLP, GCP, FDA Regulations, Medical Device

Medical & Clinical Laboratory Technologist

Professional Summary Shows consideration for individual patients and their needs. Observes all safety and infection control protocols. Enthusiastic and capable of working independently as well as cooperatively. Remains very well organized and maintains thorough and accurate records. Consistently demonstrates poise and control when performing duties under pressure and handling stressful situations. Persistent, organized and ...

Tags for this Online Resume: Electrophoresis, Cellular, ELISA, Immunology, Microbiology, Clinical Research, COLI, Research

Clinical Research Associate - 5+ Years of Experience

Experienced with key clinical trial systems including CTMS, EDC, IVRS and eTMF systems,Recist1.0,ECOG,statistical concept

Ideal Companies: Roche, Pharm-Olam

Tags for this Online Resume: Clinical Research, Compliance, Documentation, Research, Good Clinical Practices, Management, Oncology, Protocol, Cardiovascular, Data Management, CTMS, EDC, SAE reporting

Clinical Research - 1 Years of Experience - Near 27106

I am actively seeking an entry-level position as a scientist, to enhance my professional growth by providing challenging career while utilizing my existing knowledge and skills.

Tags for this Online Resume: Adobe, Adobe Photoshop, Compliance, Focus, Gateway, Good Clinical Practices, ICH, Imaging

Clinical Research - 6 Years of Experience - Near 75287

PROFESSIONAL SUMMARY: A CRA with strong eye for detail and exceptional ability to interpret and follow instructions Possesses the ability to collect accurate data in line with client specifications excellent analytical and organizational skills knowledgeable in FDA regulations, GCP/ICH guidelines, seeking to join an organization that makes research subjects' safety its first priority. CORE QUALIFICATIONS: * Over 5 years exp...

Tags for this Online Resume: Management, Clinical Research, Data Management, Protocol, Research, Assessments, Forth Programing Language, Good Clinical Practices, Monitoring, Training

Clinical Research - 15 Years of Experience

Focused on obtaining a position as a Clinical Research Associate. Detail oriented with the ability to plan organize coordinate and manage projects according to priorities. Ongoing and consistent promotion of team work efforts. Excellent Communication and Interpersonal skills. Excellent oral and written communication skills with the ability to communicate effectively with medical personnel. Quick learner with the ability to ...

Tags for this Online Resume: Documentation, Management, Cardiovascular, Cardiology, Clinical Research, Distribution, Good Clinical Practices, Research