CV, Curriculum Vitae and Online Resumes Search

Recruiters - Try Postings!

Postings.com™ is a must-have for recruiters who want to:

  • Find Qualified Candidates
  • Find Job orders and Post Splits
  • Be Found in Search Engines
  • Implement a Social Sourcing Strategy
30-Day Free Trial!



Job Seekers - Look Here!

Hitting a wall with your job search? Try Climber Premium.

  • Top the Search Engines
  • Unsurpassed Candidate Marketing
  • Power Career Networking
  • Fresh Jobs from the Net

Were you looking for Consent job results?
Click Here to search for Consent in our 2.4M jobs.



Online Resumes with "Consent"



Project Leader

Manage a team of results-driven staff preferably with a Statewide Automated Child Welfare System (SACWIS)project

Ideal Companies: Information Technology; Government; SACWIS Projects

Tags for this Online Resume: Technical writer, functional analyst, documentation manager, quality assurance, project leader, SACWIS experience, implementation lead, policy writer

Goal focused Quality Leader in medical devices and pharmaceuticals

Began career with 10 years with the FDA in the Detroit District office and at the Kalamazoo, MI and Grand Rapids Resident Posts. Conducted inspections at pharmaceutical and medical device companies, conducted investigations and testified in court. I Left for a start-up medical device contract manufacturer where I developed the quality system and initiated 510(k) submissions. I also identified and resolved problems result...

Ideal Companies: Small to large medical device or pharmaceutical companies such as Abbott Laboratories, Baxter, CR Bard, Phillips, Medtronic, Boston Scientific, St. Jude Medical, Johnson & Johnson, Bausch and Lomb.

Tags for this Online Resume: Quality Systems Management, Regulatory Compliance, ISO 9001:2000/ISO 13485:2003, Pharmaceutical GMPs

Featured Profile

Featured Profile

Research Analyst I-12 years experience

To get a position in Clinical Research. Excellent medical background, ability to recruit Patients for a study, initiate a study, working with IRB on Protocols and Consent, writing Incident and other reports and working on budgeting.

Clinical Research Professional - Specializing in Study Start Up

I am ready to take my career to the next level. I am a Clinical Research professional specializing in Study Start Up with experoence in: ICFs, Site Regulatory Packages, ICH-GCP, Feasibility and Contract Negotiation.

Tags for this Online Resume: ICH-GCP, Study Start Up, Informed Consent, Contract Site Agreements, Feasibility , Regulatory Documents

Featured Profile

Certified Clinical Research Coordinator

To obtain a position as a clinical research coordinator

Ideal Companies: Genentech

Tags for this Online Resume: GCP's, CRF's, Resolve queries, Consent study participants

Clinical Research - 7 years experience - Registered Dental Hygienist with managerial skills

I am looking for a position in clinical research to expand a company research group with my expertise and experience from a pharmaceutical and clincial site aspect. From monitoring, to writing protocals and informed consents, IRB submissions, in house clinical examiner to writing training powerpoints, I have many aspects of experience to offer.

Tags for this Online Resume: clinical, research, monitoring

Featured Profile

Educational Consultant: Bilingual Education, TESOL/ESL

Achieves marketing and sales operational objectives by contributing marketing and sales information and recommendations to strategic plans and reviews; preparing and completing action plans; implementing production, productivity, quality, and customer-service standards; resolving problems; completing audits; identifying trends; determining system improvements; implementing change. Plan, design lessons, and deliver instruct...

Tags for this Online Resume: Higher Education Teacher, Consultant, Professional Developmentt, Manager, Director, Dean

Regulatory Compliance Specialist

Ideal Companies: MedImmune, NIH, Social & Scientific Systems

Tags for this Online Resume: triage, clnical trials, auditing, informed consents, study protocols, communications