Clinical Research Scientist / Senior CRS Job occupation at Celgene Corporation in Summit

Celgene Corporation is at present recruited Clinical Research Scientist / Senior CRS Job on Thu, 16 May 2013 12:31:13 GMT. Post by Jobing - Job Title: Job ID: 13929Location: Summit, NJOffsite Territory: Full/Part Time: Fullâ€"TimeRegular/Temporary: RegularCategory: ClinicalDepartment: Hematology/Oncology â€" 3606Celgene Corporation is committed to delivering innovative therapies designed to improve the lives of patients worldwide. We are a global biopharmaceutical company with operations in more than 70 countries that is...

Clinical Research Scientist / Senior CRS Job

Location: Summit New Jersey

Description: Celgene Corporation is at present recruited Clinical Research Scientist / Senior CRS Job right now, this occupation will be placed in New Jersey. More complete informations about this occupation opportunity kindly read the description below. Post by Jobing - Job Title: Job ID: 13929Location: Summit, NJOffsite Territory: Full/Part Time: Fullâ€"TimeRegular/Temporary: R! egularCategory: ClinicalDepartment: Hematology/Oncology â€" 3606Celgene Corporation is committed to delivering innovative therapies designed to improve the lives of patients worldwide. We are a global biopharmaceutical company with operations in more than 70 countries that is helping to turn incurable cancers into chronic, manageable conditions. We are seeking talented professionals as we continue to grow and advance our efforts in oncology, hematology and immune and inflammatory disease. If you would like to join a company where you can make a difference, please consider the Celgene family.Degree in Life Sciences (e.g., BS in nursing, pharmacy or related medical field), 5â€"10 years experience in clinical research development or equivalentResponsibilities will include, but are not limited to, the following: 1.

Assist the Clinical Research Physician to interface with study/clinical team members including: Clinical Operations, Data Management, Statistics, Drug Safet! y, Regulatory and Project Management.2. Prepare or assist with! preparation of key documents e.g. Investigator Brochures, FDA Briefing Documents, internal or external presentations, etc.3. Review literature and prepare summary documents for inclusion in IB, protocols, Briefing documents, etc.4.

Participate in Development Planning for assigned compounds.5. Protocol preparation (writing, reviewing and crossâ€"functional facilitation as appropriate).6. Assist with review of ongoing summary data including: safety, primary efficacy variables, laboratory data.7. Clinical study report preparation.8.

Assist Clinical Research Physician to make recommendations, take action and provide clinical research expertise related to projects.Skills/Knowledge Required: â€" Minimum 2â€"5 yrs. experience in medical or technical writingâ€" Extensive medical/scientific and clinical research knowledgeâ€" Knowledge of Clinical Date Reviewâ€" Knowledge of protocol design, implementation and proficient at data interpretationâ€" Experience in prot! ocol development, study report preparation, Investigator Brochure preparation, IND safety updatesâ€" Experience in all aspects of the drug development process (device & tissue experience an added benefit)â€" Knowledge of GCP and ICH Guidelinesâ€" Experience in presenting at Investigator Meetingsâ€" Detailâ€"oriented, wellâ€"organizedâ€" 35% travel requiredâ€" Ability to assimilate technical information quicklyâ€" Proficient in Microsoft Word, Excel, PowerPoint; Microsoft projectâ€" Demonstrated ability to work as part of a teamâ€" High level of interpersonal and communication skills (written and verbal)Celgene is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.Celgene complies with all applicable national, state and local laws governing nondiscrimination in emp! loyment as well as employment eligibility verification requirements of ! the Immigration and Nationality Act. All applicants must have authorization to work for Celgene in the U.S.Employment applicants requiring immigration sponsorship must disclose, when initial application for employment is made, whether or not they are legally authorized to work in the U.S. and, if so, whether that authorization permits them to work in the job they seek.

In no case should Celgene support of a potential employee's temporary visa application be construed to guarantee success of that application or amend or otherwise invalidate the "atâ€"will" employment relationship between the employee and Celgene.*LIâ€"KM1
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If you were eligible to this occupation, please email us your resume, with salary requirements and a resume to Celgene Corporation.

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This occupation starts available on: Thu, 16 May 2013 12:31:13 GMT



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