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PRODID:-//Cancer Epigenetics Society - ECPv5.3.2.1//NONSGML v1.0//EN
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X-WR-CALNAME:Cancer Epigenetics Society
X-ORIGINAL-URL:https://ces.b2sg.org
X-WR-CALDESC:Events for Cancer Epigenetics Society
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TZID:Europe/Paris
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DTSTART:20180325T010000
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DTSTART:20181028T010000
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DTSTART;VALUE=DATE:20180417
DTEND;VALUE=DATE:20180519
DTSTAMP:20260729T172150
CREATED:20180417T124241Z
LAST-MODIFIED:20180417T124241Z
UID:19871-1523923200-1526687999@ces.b2sg.org
SUMMARY:Senior Scientist - Toxicology
DESCRIPTION:The Senior Scientist\, Toxicology reports to the Head of Nonclinical Development and serves as an integral contributor to all the nonclinical development projects at Epizyme. The Senior Scientist provides expertise and advice to guide the activities of a project\, and provides scientific/technical expertise. Viewed as expert in the field within the department. Accountable for the development and implementation of solutions to problems. May develop new approaches and applications of programs and systems to lead processes in a new direction. Works independently toward goals and objectives of the department. \nResponsibilities \n\nExecution of nonclinical safety evaluations to further drug discovery and development objectives\nDevelop\, and execute nonclinical safety development plans from discovery through late stage clinical development programs\nParticipation on discovery and development teams\nCommunication and collaboration with program teams and across functions (e.g. Biology\, Clinical\, DMPK\, Medicinal Chemistry\, CMC\, etc.) to allow successful management of toxicology plans\nFrequent contacts with functional area leads and outside collaborators. Represents toxicology group in providing solutions to difficult technical issues associated with specific projects.\nProvide strategic advice for drug development programs\nPreparation of nonclinical safety assessment portions of regulatory documents\nManage toxicology contract research organizations (CROs): i.e. selection\, evaluations\, timelines\, communication\, monitoring and budget\nDesign toxicology study protocols\, monitor and review studies conducted at CROs\, provide integrated data evaluation and interpretation\nCommunicate nonclinical safety data with the proper perspective to appropriate team and management forums within Epizyme and to external partners\, as appropriate\n\nRequirements \n\nMS/PhD in toxicology or related field with a minimum 5-7 years’ industry experience\, Strong scientific background in pharmacology and toxicology\, In depth knowledge of nonclinical drug development and regulatory requirements\nStrong organizational skills\, ability to multi-task\, flexible to change\nSuperior communication skills (both written and oral)\, attention to detail\, and good questioning and analysis techniques desired\nDemonstrated ability to continually expand knowledge base and open to learning from\nothers\nGoal oriented\, highly self-motivated and self-directing individual who enjoys working in different environments and multiple capacities\nDemonstrated ability to work collaboratively with various functional areas\nExperience with contracting CRO studies and effective communication with CROs to enable a quality working relationship\, resulting in a quality product/report\nMust work effectively in a team environment and with individuals at all levels within an organization\nExperienced in preparation and review of regulatory documents\nSome travel required
URL:https://ces.b2sg.org/event/epizyme-17apr18/
LOCATION:Epizyme\, 400 Technology Square\, Cambridge\, MA\, 02139\, United States
CATEGORIES:Jobs
ATTACH;FMTTYPE=image/jpeg:https://ces.b2sg.org/wp-content/uploads/2017/06/epizyme.jpg
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