Clinical Research Physician (Phase I)

Covance Inc Located in: San,Houston,Dallas,  Texas
(Private and Secure - Guaranteed!)

Covance Inc Biotechnology Jobs Pharmaceutical Careers
 

JOB DESCRIPTION

Get ready to redefine what’s possible and discover your extraordinary potential at Covance. Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.

Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career.

 

Covance is seeking a Clinical Research Physiican for in our Phase I Research Facility located in Dallas.  As a Clinical Research Physician, you'll be responsible for the following:

 

A. Duties and Responsibilities:

• Responsible for protecting the rights, safety and welfare of participants under their care.

• Responsible for ensuring that the clinical trial is conducted according to the investigational plan and all applicable regulations. • Provide medical and scientific feasibility of all new sponsor inquires.

• Direct test article administration or dispensation.

• Review and evaluate protocols and provide clinical and scientific support.

• Liaise with sponsor regarding study design and site capabilities.

• Interact with regulatory bodies as is relevant to clinical operations.

• Attend study initiation meetings.

• Present protocols at IRB/IEC meetings, as required.

• Assist Operations and Client Managers with sponsor visits.

• Perform pre-study physical examinations and review lab data to ensure volunteers are medically and mentally fit upon entering the study.

• Perform on-study and post-study physical examinations to ensure that the physical and mental well being of volunteers is undiminished at the end of the study.

• Inform Principal Investigator, IRB and Sponsor as appropriate of relevant events.

• Review and sign CRFs at the conclusion of the study.

• Delegate the above as appropriate.

• Act as Principal Investigator/Co-Investigator as assigned by the Medical Director

Required:

• Active M.D or DO License and DEA license

 CPR/AED Certified

3-5 years clinical experience as practicing physician

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CRITICAL REQUIREMENTS

COMPANY INFORMATION

Covance Inc. is proud to be the only drug development company with a full range of research and development services—from lead optimization, to commercialization and life cycle management. Covance, headquartered in Princeton, NJ, is the drug development business of LabCorp with global operations in more than 30 countries.

JOB INFORMATION

Seniority Level:
Experienced - Not Management
Function:
  R&D / Science
Preferred Industry Background:
 
Managing a team of:
N/A
Required Travel:

Base Salary:
Confidential
Bonus:
Benefits:
Other Compensation: