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eTeam Inc.Round Lake (IL)
Title: Research Associate Scientific II
Location:- Round Lake, IL
Duration: 6+ Months
Pay Rate Range:- $35.00 - $38.00 on w2
Summary:
This position is responsible for analytical testing, validation/verification, and/or transfer of test method...
AbbVieNorth Chicago
Job Description
AbbVie (NYSE:ABBV) is a global, research-based biopharmaceutical company formed in 2013, following separation from Abbott. AbbVie combines the focus and passion of a leading-edge biotech with the expertise and capabilities of a long...
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AssistRxChicago
The Senior Account Manager cultivates and maintains AssistRxs relationship with our Pharmaceutical manufacturing partners. In this role, youll be working with pharmaceutical executives (Associate Director and above) on a daily basis to ensure...
AssistRxChicago
The Senior Account Manager cultivates and maintains AssistRxs relationship with our Pharmaceutical manufacturing partners. In this role, youll be working with pharmaceutical executives (Associate Director and above) on a daily basis to ensure...
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Clinical research scientist
Randstad | Clark | www.randstadusa.com |
job summary:
Under the supervision of a clinical project manager, perform clinical studies to support clinical innovation programs related to skin biology.
location: Clark, New Jersey
job type: Contract
salary: $40 - 45 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
• Assist clinical team members in various aspects of clinical study, including e-monitoring of eCRF system, compiling study results and images, and QA/QC of study reports.
• Maintain and track all clinical team instruments and laptops. Ordering, shipping and labelling of study products to meet study timeline.
• Maintaining strong relationships with internal and external partners (CROs, global Advanced Research, Data Management Team, and Statistical Team), to ensure clinical study integrity.
• Serve as key Quality person in the team, to ensure compliance with global Quality guidelines and GDPR regulation.
qualifications:
• Bachelor degree in related field with 3-5 years of relevant working experience.
• Minimum of 1 year experience in managing and monitoring Human Clinical Trials in pharmaceutical, OTC, or personal care industries.
• Experience working with CROs; Solid understanding of good clinical practices and FDA guidelines;
• Working knowledge on methods of evaluation (instrumental and clinical) or diagnostic tools for evaluating product efficacy would be a plus.
• Good knowledge of Skin biology, and Dermatology.
• Strong communication, presentation and project management skills.
• Be able to work independently and to drive the projects forward with minimum supervision.
skills: Clinical research, GCP (Good Clinical Practice)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
Applications accepted on ongoing basis until filled.
Under the supervision of a clinical project manager, perform clinical studies to support clinical innovation programs related to skin biology.
location: Clark, New Jersey
job type: Contract
salary: $40 - 45 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
• Assist clinical team members in various aspects of clinical study, including e-monitoring of eCRF system, compiling study results and images, and QA/QC of study reports.
• Maintain and track all clinical team instruments and laptops. Ordering, shipping and labelling of study products to meet study timeline.
• Maintaining strong relationships with internal and external partners (CROs, global Advanced Research, Data Management Team, and Statistical Team), to ensure clinical study integrity.
• Serve as key Quality person in the team, to ensure compliance with global Quality guidelines and GDPR regulation.
qualifications:
• Bachelor degree in related field with 3-5 years of relevant working experience.
• Minimum of 1 year experience in managing and monitoring Human Clinical Trials in pharmaceutical, OTC, or personal care industries.
• Experience working with CROs; Solid understanding of good clinical practices and FDA guidelines;
• Working knowledge on methods of evaluation (instrumental and clinical) or diagnostic tools for evaluating product efficacy would be a plus.
• Good knowledge of Skin biology, and Dermatology.
• Strong communication, presentation and project management skills.
• Be able to work independently and to drive the projects forward with minimum supervision.
skills: Clinical research, GCP (Good Clinical Practice)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
Applications accepted on ongoing basis until filled.
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