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Online Resumes with "Patient Recruitment"



Featured Profile

Clinical Research Coordinator - 10 years experience - Harrisburg, PA

I am a highly experienced Clinical Research Coordinator (CRC) who has worked in the medical research field for 10 plus years. As both a CRC and a Project Manager I possess a background built on a strong foundation of self-motivation, team work and a dedication to the improvement of medical and healthcare services. I have experience in all aspects of medical research from the development, implementation and regulatory compli...

Tags for this Online Resume: Harrisburg, Pennsylvania, Clinical Research, Research Associate, CRA

Featured Profile

Clinical Research - 6 Years of Experience - Near 92649

Experienced Clinical Research Professional interested in positions within the pharmaceutical or medical device industry.

Ideal Companies: inventiv, johnson & johnson, covance, covidien, peregrine

Tags for this Online Resume: Irvine, CCRP, regulatory affairs, clinical project manager, EDC, budgets , timelines, contracts and budgets

Featured Profile

Clinical Research - 15 Years of Experience - Near 90001

I am seeking a position in Clinical Trial Management or as a Project Manager per my previous US and international experience.

Ideal Companies: Pharmaceutical or Biotech

Tags for this Online Resume: Oncology, Orthopedics, Surgical, Clinical Research, Management, Medical, Medical Affairs, Diabetes, Cardiovascular, Women's Health, Clinical Trial Management, Regulatory, Medical Writing, Microsoft, CTMS

Clinical Research - 14 Years of Experience

ACCOMPLISHMENTS ACROSS THE CAREER * Successfully manage global CRO within a short span time - turn around trial performance. * Achieved 50% surge in recruitment and ensured recruitment rate for 20+ months by turning around in a challenging trial in an oncology area. * Implemented recruitment strategy in an on-going trial that resulted in 100% achievement to planned patient recruitment in a rheumatology indication. * Bagged ...

Tags for this Online Resume: Management, Planning, Project Management, Project Manager, Proposal Development, Quality, Quality Assurance, Test

Clinical Research with 7 years of experience in medical field for different positions - Near M1G 3S4

Actively looking for an opportunity to work as a Clinical Research Coordinator. Recently completed the Placement as a Clinical Research Trainee from Toronto Rehabilitation Institute (UHN), Toronto on Sep 30, 2016. Key-Skills: * Possesses Post graduate Diploma in Clinical Research with medical background and experience of working in health field for more than 7 years * Well-developed time management skills and excellent atte...

Tags for this Online Resume: Data Entry, Medical, Health Awareness, Training, Cardiopulmonary resuscitation (CPR), Clinical Research, Phlebotomy, ICH-GCP Guidelines, Pharmaceutical Industry, Patient Recruitement, Clinical Trial

Clinical Research Associate

SUMMARY: To apply my knowledge of FDA Good Clinical Practice guidelines/ICH guidelines, extensive site/field Clinical Director, Site Lead Study Management, in addition to my experience with various therapeutic areas of medicine, to a position as a Clinical Research Associate. AREAS OF EXPERTISE * Management * Interview candidates and either make a selection decision or recommend individuals for hire. * Able to manage multip...

Tags for this Online Resume: Clinical Research, Research, Accounting, Acquired Immune Deficiency Syndrome (AIDS), Advertising, Amazon Elastic MapReduce, Audit, Basic First Aid, BLS, Budgeting

Clinical Research

Summary of Qualifications Clinical Research Manager, Associate, Monitor, Coordinator, with over 25 years experience in the medical field and 21 years experience in clinical trials with extensive experience in the fields of Cardiology, Electrophysiology, Neurology, Urology, Autoimmune, Respiratory, Gastroenterology, Weight Loss, Diabetes, Women's Studies, Arthritis, COPD, Gynecology, Endocrinology, Rheumatology and Stem Cell...

Tags for this Online Resume: Monitoring, Protocol, Cardiovascular, Clinical Research, Management, Pharmaceutical, Research, Therapy, Audit, Data Management, Medical Device, CRA, CTM, Clinical Trials

Director

QUALIFICATIONS: Over twenty years drug development experience ranging from pre-clinical pharmacology / toxicology to managing and directing clinical and cross functional teams in the conduct and execution of global, clinical trials. Experience includes coordinating and planning for budgeting, resourcing, drug supply, site and sponsor audits, and global regulatory submissions. Management experience includes management of in-...

Tags for this Online Resume: Data Management, Management, Nephrology, Clinical Research, Clinical Study Reports, Drafting, Oncology, Project Management, Project Manager, Protocol

Life Scientist - 5 Years of Experience

Profile I am an enthusiastic, dynamic and analytical graduate with previous experience in teaching integrated science, medical laboratory tests, community development activities in the area of HIV prevention and reproductive health supported by UNICEF and patient recruitment for scientific study. I have also gained customer service, sales, administrative and relationship management experience in the Life Insurance and Suppl...

Tags for this Online Resume: Health Care Industry, Analytical Skills, Benefits, Biotechnology, BPS, Business Plan, Community Development, Complaints, Customer Service, Development Activities, Cell Gulture, Immunocytochemistry, HPLC

Postsecondary Teacher - 11 Years of Experience - Near 29376

CURRICULUM VITAE: Sharon Woodruff Team excellence instructor, facilitator, and trainer. Proven managerial, interpersonal, and training skills. Work History Title: Senior Clinical Research Associate Company/Location United BioSource Corporation Kansas City, MO/Regional United States Dates July 2014 - January 2015 Accountabilities Implement and monitor clinical trials for medications and devices to ensure sponsor and invest...

Tags for this Online Resume: South Carolina, Training, New Hire , Business, Education, Postsecondary, Excellence

Clinical Regional Monitoring - 3 Years of Experience - Near 0000

PROFESSIONAL SUMMARY Clinical Research Professional with various project experience from concept to development. Talents include in-depth knowledge of ICH guidelines SAE reporting and GCP auditing. Integral team-player with excellent communication skills CORE QUALIFICATIONS * Patient Recruitment & Screening * Detailed Documentation * Serious Adverse Event Reporting * Communicating with IRB for study proposal, approval and u...

Tags for this Online Resume: Clinical Research, Data Entry, Research, Audit, Communication Skills, Compliance, Documentation, Excellent Communication Skills, Good Clinical Practices, ICH