Pharmacology and Toxicology - DABT Senior Director

Confidential Company  •  San Rafael, CA and San Francisco, CA

11 - 15 years experience  •  Biotech/Pharma

$240K - $290K
Posted on 11/08/17
Confidential Company
San Rafael, CA
11 - 15 years experience
Biotech/Pharma
$240K - $290K
Posted on 11/08/17

Full Time - Permanent Job

Compensation:

$240,000 to $290,000 + Full Benefits + Relocation Assistance + Bonus

Interview Travel Reimbursed - Yes

?RESPONSIBILITIES: 

Contribute to and implement an overall drug development strategy to support nonclinical and clinical pharmacology development plans in support of all stages of drug development.

Design, implement, report and interpret nonclinical study data to support small molecules and biologics in late-stage research and all stages of nonclinical/clinical development.

Prepare study proposals, protocols, study reports and regulatory documents to support nonclinical development of drug candidates.

Managerial responsibilities include supervision of Pharm/Tox scientific staff and team development Interact with CROs, university laboratories, analytical laboratories, collaborators, both internal and external to, as necessary to ensure appropriate/timely progression of nonclinical projects.

Collaborate with various departments to ensure efficient cooperation with across functional areas.

Effectively communicate nonclinical findings and their relevance to senior management, project teams, collaborators, and regulatory agencies (i.e. FDA, EMEA, MHRA, ROW).

Participate in multi-disciplinary drug development teams and lead sub-teams.

Excellent written and verbal communication skills.

Ability to build and foster productive cross-functional collaborations both within and external.

Prepare study synopses, protocols, study reports and regulatory documents to support nonclinical development of drug candidates Interact/collaborate with various functions, CROs, university or analytical laboratories, business partners, as necessary to ensure appropriate/timely progression of projects.

?EXPERIENCE: 

A minimum of ten years of nonclinical experience in the pharmaceutical and/or biotechnology field.

A minimum of seven years of management responsibility Strong understanding of drug development.

Excellent written and verbal communication skills.

Ability to build and foster cross-functional collaborations both within and external to.

Established ability to interact with various regulatory agencies.

Established Drug Development Reputation Experience to support development of both small molecules and biologics.

Strong understanding of FDA and OECD.

Good Laboratory Practices.

Veterinarian pathology experience strongly required.

?EDUCATION: 

Required: Doctorate (Ph.D.) in toxicology or closely related field of study.

Board Certification in Toxicology is a plus. 

AND/OR Veterinarian (D.V.M.) with Board Certification in Pathology 

?CANDIDATE DETAILS

10+ to 15 years experience

Seniority Level - Executive

Management ExperienceRequired - Yes

Minimum Education - Doctorate Degree

Willingness to Travel - Occasionally

SCREENING QUESTIONS

Candidate has a current DABT Designation

Candidate has extensive drug discovery & development experience across modalities: small and large molecules, etc

Experience in gene therapy

Wants to serve as a Leader / Mentor to Scientific team

Not the right job?
Join Ladders to find it.
With a free Ladders account, you can find the best jobs for you and be found by over 20,0000 recruiters.