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Online Resumes with "Clinical Site Monitoring "
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
Clinical Research Associate
Highly motivated and experienced biomedical professional with expert knowledge and proficiency in clinical research monitoring. A certified CRA. Hands-on experience in the clinical investigations of novel pharmacological products. Eager to translate expertise gained in research and monitoring to measurable success in the field clinical studies. A demonstrated record of academic achievement and recognition, accompanied by e...
Tags for this Online Resume: Clinical Site Monitoring , Identification and interviewing of potential investigators, ICH GCP Training , Adverse Event Reporting, Study Planning Activities
Clinical Research
Experienced Clinical Research Associate seeking a challenging and rewarding Clinical Research Associate (CRA) position that will utilize my clinical site monitoring and general management skills and experience to coordinate, monitor and manage all aspects of clinical trials in accordance with the ICH-GCP guidelines, FDA regulations, standard operating procedures and study protocol.
Corporate Recruiter - 9 Years of Experience - Near 21057
QUALIFICATIONS SUMMARY Proven top performer with exceptional interpersonal and communication skills. Collaborates and builds relationships effectively with all levels of leadership to address business challenges and organizational staffing needs. Proven ability to recruit passive candidates and approach the "un-approachable candidate" both domestically and internationally. Infor Global: November 2015 - May 2017 Contract Pos...
Tags for this Online Resume: Full life cycle, Infor, Insurance, Java Programming Language, Leadership, LinkedIn Recruiter, Management, Microsoft, Microsoft Office, Networking, recruiter, recruiting, employee relations
Clinical Research - 1 Years of Experience - Near M1W 2T1
Foreign-trained medical doctor and clinical research professional with CRA Professional Development Clinical Site Monitoring & ICH GCP Training. Experienced in clinical study files review to ensure accuracy of all the documented data including ME & AEs. Comprehensive knowledge of clinical research methodology and proficient in Phase I-IV clinical studies and ICF processing and study protocols. Excellent time management and ...
Tags for this Online Resume: Toronto, Canada, Strong Clinical Trials & Medical Management background, Detail Oriented, Data Review, Clinical Trials Supervision, Team player, Quick Learner, Certified CR Professional with Medical Background, Compliance, Documentation, clinical, research, phase i, phase ii, clinical trials, phase iv, pharmaceutical, cro
