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Associate Director/Director, Diligence

HCPro, Inc.

This is a Contract position in Cambridge, MA posted April 30, 2020.

The Associate Director/Director, Diligence is a critical position, responsible for managing processes for tracking and reporting of programs under evaluation for potential acquisition/license by Boston Pharma and for Boston assets being outlicensed.

This person will ensure the use of streamlined processes used by Boston Pharma for internal and external diligence are maintained and will develop and maintain project tracking tools.

They will optimize standardized templates, and lead meetings to fully assess project risks and develop mitigation strategies.

They will also support the use of CROs for scientific diligence/confirmatory studies for potential assets under evaluation.

They will enable the orderly transfer of data and knowhow from originators of programs acquired by Boston Pharma into Boston’s internal systems.

The AD/Dir, Diligence may also support diligence for externalization of Boston programs.

The position requires excellent leadership and networking capabilities to maximize the use of external resources (CRO’s, CMO’s, KOL’s, etc.) and integration with internal domain expertise, as well as an extremely strong understanding of drug development and its various risks.

With the ED of Diligence, define project objectives and requirements necessary to structure diligence projects Develop processes, manage timelines, and drive activities for inbound and outbound diligence Enable diligence strategies to optimize use of resources to ensure multiple diligence projects can be maintained under tight timelines Develop and maintain standardized templates to deliver timely, high-quality, and transparent diligence findings Maintain a best-in-class network of external experts to support evaluation of assets outside of Boston Pharma’s core expertise Depending on asset stage, manage nonclinical studies at CROs to support diligence evaluation Oversee the orderly transfer of external data to Boston Pharma after deal closing and ensure that all files (and related material) are properly organized and maintained Maintain active knowledge of large pharma requirements regarding due diligence Maintain knowledge of best practices relating to due diligence Manage data rooms for active Boston Pharmaceuticals programs Requirements Qualifications: PhD degree or equivalent education, in a science or health-related discipline Strong project management skills and general understanding of project management tools; e.g.

MS Project Excellent communication and organizational skills and attention to detail At least 2-5 years hands-on experience in preclinical research or clinical research in biotech/pharma industry Experience with preclinical development, preferably a track record of supporting CTA/IND submissions Ability to perform in fast-paced, dynamic, constantly evolving environment Strong team player: demonstrated ability and willingness to work on a team, assist team members as needed and accomplish tasks required to achieve goals Job Information Job ID: 53786136 Location: Cambridge, Massachusetts, United States Company Name: Boston Pharmaceuticals Job Function: Business Development, Data Analysis, Project Management Job Type: Full-Time Job Duration: Indefinite Min Education: Ph.D.

Min Experience: 2-3 Years Required Travel: 0-10% Jobs You May Like Sr.

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