1+ months

Director, Clinical Research

Cambridge, MA 02139
**Role Summary and Responsibilities**

To lead development of one or more clinical trials and deliver innovative and informative study designs in Hematologic and other related metabolic indications in alignment with overall project and clinical plan and in collaboration with RU and partner line functions

To perform systematic high quality evaluation and interpretation of study safety and other relevant data in collaboration with the study physician

**Basic Qualifications**

Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

Graduate degree with 7+ years of clinical research experience in industry and academic settings in all phases of development.

Experience or established knowledge in hematology, metabolic or related disease area

Postgraduate scientific / medical training.

GCP training and track record of design, oversight and interpretation of clinical trials.

Familiarity with related disciplines (e.g., biostatistics, regulatory, pre-clinical pharmacology, pharmaceutical sciences).

**Preferred Qualifications**

Demonstrated leadership in design, initiation, conduct, and reporting of clinical trials in both industry and academic settings.

Comprehensive understanding of global drug development with particular emphasis on complex clinical trials involving unique efficacy endpoints (e.g., clinical functional assessments, imaging).

Robust knowledge of scientific and clinical principles and ability to work across therapeutic areas, ideally with a focus on rare disease, pediatrics, and neuromuscular disorders (e.g., Duchenne muscular dystrophy) .

Skill in review and interpretation of emerging safety and efficacy profile of drug candidate.

Proficiency in collaborative and constructive issue resolution across functions.

Proven scientific writing skills with strong interpersonal written and verbal communication skills, including ability to evaluate and present complex data to colleagues and stakeholders at various levels and disciplines.

Working understanding and ability to offer instruction of worldwide research and development (WRD) infrastructure and processes (e.g., Pfizer SOPs, goals, and policies on business conduct).

Preferred established leadership in other aspects of clinical trial execution, inclusive of site coordination, clinical operations/project management, and quality assurance.

**Other Job Details:**

+ Eligible for Relocation Package

+ Eligible for Employee Referral Bonus

+ **\#LI-PFE**

**Sunshine Act**

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

**EEO & Employment Eligibility**

Pfizer 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. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Posted: 2019-11-05 Expires: 2020-03-07

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Director, Clinical Research

Cambridge, MA 02139

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