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Clinical Research Manager
| Details |
Country: USA
Location: California-Ventura County Thousand Oaks, CA
Total applied: 30 Job Category:Biotech/R&D/Science
Relevant Work Experience:5+ to 7 Years
Education Level:Bachelor's Degree
Location:Thousand Oaks, CA
Status:Full Time, Employee
Occupations:Biological/Chemical Research;Clinical Research;Pharmaceutical Research
Career Level:Experienced (Non-Manager)
Relevant Work Experience:5+ to 7 Years
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Clinical Research Manager
Chiltern International is a well established global contract research organization with offices throughout Europe, North America and India. We were established in 1982 and have served pharmaceutical, biotechnology, and device companies in over 38 countries worldwide. Due to our continued growth, Chiltern is seeking a highly motivated individual to join us as a Clinical Research manager. Candidates can be located in Thousand Oaks or in San Francisco, CA.
The qualified candidate will have:
Basic Qualifications
· BA/BS/BSc or RN
· 5 years work experience in life sciences or medically related field, including 2 years of biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company)
Preferred Qualifications
· BA/BS/BSc in the sciences or RN
· 7 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience ( clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company)
· Previous management experience of direct reports
· Experience at, or oversight of, outside clinical research vendors (CROs, central labs, imaging vendors, etc.)
Essential job functions include:
· Planning, management, and reporting of clinical studies conducted by Global Development through oversight of cross-functional study activities, identification and resolution of issues, and communication of study timelines/deliverables
· Ensuring implementation of study(ies) in accordance with SOPs and ICH/GCP guidelines
· Contributing to study concept documents, protocols, clinical study reports
· Management of study budget, timelines, and insourcing / outsourcing partners to the required standards
Required skills and abilities include:
·Good computer literacy with working knowledge of PCs, Windows and Microsoft Office applications
·Good oral and written communication and co-ordination skills with the ability to conduct meetings
· Experience working in a team environment under time and resource pressures
Chiltern’s unique corporate culture encourages a healthy balance of personal life and work. We offer an excellent salary and benefit package to include medical, dental, vision, company matching 401K, excellent vacation & holiday, paid life insurance, AD&D, long and short term disability and many other employee incentives. If you have the experience required and feel you are the dynamic person we are looking for, please forward your resume in a Word document via email to: tripp.smallwood@chiltern.com
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