Senior Director, Clinical Operations

Highly Competitive Salary
  1. Permanent
  2. Program Manager / Director
  3. United States
New York, USA
Posting date: 20 Dec 2019
CR.SC.27022
This vacancy has now expired

Proclinical is currently recruiting for a Senior Director of Clinical Operations for a biotechnology company located in New York, NY. Successful candidate will provide strategic and operational expertise for the timely, quality preparation and execution of Tessa's multi-country sponsored clinical development programs (Phase 1 - 3).

Job Responsibilities:

  • Accountable for the implementation and execution of Clinical Operations product-specific strategic and tactical plans
  • Ensure the effective and constructive integration of clinical operations knowledge and expertise into all applicable clinical development activities including integrated development plans and study protocols; interact and collaborate with other department heads as appropriate.
  • Ensure consistent and successful execution of all operational aspects of global studies as appropriate, data delivery and reporting.
  • Plan and implement Quality Checks for clinical projects and provide leadership and direction to ensure the highest standards for compliance with Company SOPs, ICH-GCP guidelines,
  • Accountable for the authorship of operational sections of protocols and investigator brochures and leading the identification of and interaction with investigative sites, including study execution.
  • Develop and maintain strong relationships with CROs, and investigators to ensure effective execution of internal and external clinical projects.
  • Responsible for the management and leadership of all staff within the Clinical Operations group including recruitment, training, career development and performance evaluations.

Skills and Requirements:

  • Bachelors or advanced degree (Ph.D. or Pharm.D.) in scientific/life-sciences or related field.
  • 15 years of clinical operations experience in pharmaceutical/drug development, with a preference for biologics experience, and including 10 years of experience in study management
  • Proven track record of planning, conducting & managing clinical operations for Phase 1-3 studies
  • In-depth understanding and experience across the clinical operations value chain, with a track record of success in study planning, execution, data cleaning, database locking, study report generation and regulatory inspection.
  • Experience in Oncology trials is required
  • Demonstrates advanced knowledge of design and phases of Oncology clinical studies on a global scale, global regulatory issues, CRO operations, and compliance practices
  • Ability to work in a very dynamic environment, handle a high volume of highly complex tasks within a given timeline
  • Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical trials, clinical study design, and data management methods.
  • Experience in conducting trials in EU is a plus
  • Ability to travel up to 30% of the time

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Susan Chapman at (+1) 646-542-0158 or upload your resume on our website - www.proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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