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
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 informed-consent job results?
Click Here to search for informed-consent in our 2.4M jobs.
Online Resumes with "informed consent"
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
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
Regulatory Compliance Specialist
Ideal Companies: MedImmune, NIH, Social & Scientific Systems
Tags for this Online Resume:
triage, clnical trials, auditing, informed consents, study protocols, communications
Clinical Research, New Jersey
Tags for this Online Resume:
Clinical Research, informed consent, CTA, CDM, IRB, TMF
Featured Profile
Clinical Research, New Jersey
Versatile business professional eager to contribute broad-scope clinical research experience toward supporting a dynamic organization.
Tags for this Online Resume:
Clinical Operations Management, Protocol and Informed Consent Quality Assurance, Management of 11 direct reports, Major: Cell Biology and Neuroscience, RDC/EDC/RAVE/HIS/CIS experience, RISK Analysis experience
Nurse- 30+ years in critical care, Clinical Research Associate-35+ years monitoring, managing Oncology,
I would like the opportunity to work with a team of research professionals. I have experience in many different clinical therapeutic fields, including Phase I studies.
Tags for this Online Resume:
Clinical Research Associate, Document Review, Write Informed consents, Clinical Team Lead, audit SOP's, electronic data review
Featured Profile
Clinical Research Associate and QA with 1 year experience and M.Sc. in Science with 10 years' experience
To get a position as a Clinical Research Professional and involve in Canada pharmaceutical industry.
Tags for this Online Resume:
ICH/GCP guidelines, FDA requirements , Design and revised protocol, Standard Operating Procedure , Case Report Form (CRF), Informed Consent Form (ICF), Adverse Events (AE) and Serious Adverse Events (SAE) , Data Managemnet, MS office, Phlebotomy, CPR, Recruit subjects
Featured Profile
Nurse Manager 10 years experience
A dedicated professional, I have more than 26 years of experience and have played variety of roles as that of staff nurse, community leader, manager, and educator.Throughout my career, I have adapted to and maintained accepted standards and procedures. . I stay abreast with the current best practices and processes followed across various organizations.
Tags for this Online Resume:
Medical Management , Nursing , Coordinator, Research, Educator, Team Leader, Cardiology, Hematology, Immunology, Management
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
Regulatory Compliance Specialist
Ideal Companies: MedImmune, NIH, Social & Scientific Systems
Tags for this Online Resume:
triage, clnical trials, auditing, informed consents, study protocols, communications
Clinical Research, New Jersey
Tags for this Online Resume:
Clinical Research, informed consent, CTA, CDM, IRB, TMF
Featured Profile
Clinical Research, New Jersey
Versatile business professional eager to contribute broad-scope clinical research experience toward supporting a dynamic organization.
Tags for this Online Resume:
Clinical Operations Management, Protocol and Informed Consent Quality Assurance, Management of 11 direct reports, Major: Cell Biology and Neuroscience, RDC/EDC/RAVE/HIS/CIS experience, RISK Analysis experience
Nurse- 30+ years in critical care, Clinical Research Associate-35+ years monitoring, managing Oncology,
I would like the opportunity to work with a team of research professionals. I have experience in many different clinical therapeutic fields, including Phase I studies.
Tags for this Online Resume:
Clinical Research Associate, Document Review, Write Informed consents, Clinical Team Lead, audit SOP's, electronic data review
Featured Profile
Clinical Research Associate and QA with 1 year experience and M.Sc. in Science with 10 years' experience
To get a position as a Clinical Research Professional and involve in Canada pharmaceutical industry.
Tags for this Online Resume:
ICH/GCP guidelines, FDA requirements , Design and revised protocol, Standard Operating Procedure , Case Report Form (CRF), Informed Consent Form (ICF), Adverse Events (AE) and Serious Adverse Events (SAE) , Data Managemnet, MS office, Phlebotomy, CPR, Recruit subjects
Featured Profile
Nurse Manager 10 years experience
A dedicated professional, I have more than 26 years of experience and have played variety of roles as that of staff nurse, community leader, manager, and educator.Throughout my career, I have adapted to and maintained accepted standards and procedures. . I stay abreast with the current best practices and processes followed across various organizations.
Tags for this Online Resume:
Medical Management , Nursing , Coordinator, Research, Educator, Team Leader, Cardiology, Hematology, Immunology, Management
Clinical Research, New Jersey
Versatile business professional eager to contribute broad-scope clinical research experience toward supporting a dynamic organization.
Tags for this Online Resume:
Clinical Operations Management, Protocol and Informed Consent Quality Assurance, Management of 11 direct reports, Major: Cell Biology and Neuroscience, RDC/EDC/RAVE/HIS/CIS experience, RISK Analysis experience
Nurse- 30+ years in critical care, Clinical Research Associate-35+ years monitoring, managing Oncology,
I would like the opportunity to work with a team of research professionals. I have experience in many different clinical therapeutic fields, including Phase I studies.
Tags for this Online Resume:
Clinical Research Associate, Document Review, Write Informed consents, Clinical Team Lead, audit SOP's, electronic data review
Featured Profile
Clinical Research Associate and QA with 1 year experience and M.Sc. in Science with 10 years' experience
To get a position as a Clinical Research Professional and involve in Canada pharmaceutical industry.
Tags for this Online Resume:
ICH/GCP guidelines, FDA requirements , Design and revised protocol, Standard Operating Procedure , Case Report Form (CRF), Informed Consent Form (ICF), Adverse Events (AE) and Serious Adverse Events (SAE) , Data Managemnet, MS office, Phlebotomy, CPR, Recruit subjects
Featured Profile
Nurse Manager 10 years experience
A dedicated professional, I have more than 26 years of experience and have played variety of roles as that of staff nurse, community leader, manager, and educator.Throughout my career, I have adapted to and maintained accepted standards and procedures. . I stay abreast with the current best practices and processes followed across various organizations.
Tags for this Online Resume:
Medical Management , Nursing , Coordinator, Research, Educator, Team Leader, Cardiology, Hematology, Immunology, Management
Clinical Research Associate and QA with 1 year experience and M.Sc. in Science with 10 years' experience
To get a position as a Clinical Research Professional and involve in Canada pharmaceutical industry.
Tags for this Online Resume:
ICH/GCP guidelines, FDA requirements , Design and revised protocol, Standard Operating Procedure , Case Report Form (CRF), Informed Consent Form (ICF), Adverse Events (AE) and Serious Adverse Events (SAE) , Data Managemnet, MS office, Phlebotomy, CPR, Recruit subjects
Featured Profile
Nurse Manager 10 years experience
A dedicated professional, I have more than 26 years of experience and have played variety of roles as that of staff nurse, community leader, manager, and educator.Throughout my career, I have adapted to and maintained accepted standards and procedures. . I stay abreast with the current best practices and processes followed across various organizations.
Tags for this Online Resume:
Medical Management , Nursing , Coordinator, Research, Educator, Team Leader, Cardiology, Hematology, Immunology, Management
Nurse Manager 10 years experience
A dedicated professional, I have more than 26 years of experience and have played variety of roles as that of staff nurse, community leader, manager, and educator.Throughout my career, I have adapted to and maintained accepted standards and procedures. . I stay abreast with the current best practices and processes followed across various organizations.
Tags for this Online Resume: Medical Management , Nursing , Coordinator, Research, Educator, Team Leader, Cardiology, Hematology, Immunology, Management
