Worldwide Clinical Trials

Associate Director, Contract Management - US - Remote

Worldwide Clinical Trials$118K — $234K *
US-AnywhereRemote in Research Triangle Park, NC
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Proficiency in MS-Office applications, especially Word, PowerPoint, and Excel.
  • Exceptional oral and written communication skills.
  • Ability to develop and manage plan schedules and deadlines.
  • Thorough understanding of corporate business practices and commercial contracting principles.
  • At least 10 years of experience in CRO or pharmaceutical data management.

Responsibilities

  • Advise on legal contract strategy and inputs.
  • Ensure submissions conform to BD requirements and sponsor requests.
  • Facilitate information distribution during contract negotiations.
  • Collaborate with various departments to align MSAs with operational agreements.
  • Develop and modify service descriptions for contracts and exhibits.
  • Manage the execution processes for MSAs, contracts, and change orders, adapting to business priorities.

Benefits

  • Equitable and transparent compensation practices.
  • Competitive benefits package dependent on location.
  • Opportunity for personal and professional growth in a meaningful industry.
Full Job Description
What the Associate Director, Contract Management does at Worldwide

The Associate Director, Legal Contracts is responsible for all aspects of contacts management for Worldwide including the company's contracts, change orders, and master services agreements (MSAs) with its sponsors and line management of Contracts Associate(s) or Managers, as assigned.

What you will do

  • Advise on legal contractual input and strategy.
  • Ensure submissions are in line with BD requirements and sponsor needs/requests.
  • Ensure appropriate information distribution and discussion with relevant operational groups during contract, change order, and MSA negotiations.
  • Collaborate with BD, therapeutic leaders, Operations and Finance to ensure the MSAs reflect what has been operationally agreed between Worldwide and the sponsor.
  • Develop and/or modify service description text in addition to original proposal text, which collectively becomes the core contract/exhibit.
  • Manage the overall process and activities for ensuring execution of MSAs, contracts and change orders, with flexibility and prioritization to meet business goals and deadlines. Re-prioritize tasks based on urgent requests.


What you will bring to the role

  • Proficiency in all MS-Office applications including Microsoft Word, PowerPoint, and a high level of proficiency with Excel.
  • Demonstrate excellent oral and written communication as well as interpersonal skills.
  • Ability to set and manage opportunity plans, communication plans, schedules, and deadlines.
  • Thorough knowledge of general corporate business practices, commercial contracting principles. Prior exposure in Proposal Development and Business Development Operations.


Your experience

  • In-depth knowledge of the CRO/pharmaceutical industry and sales support activities as well as a strong understanding of study design, project management, and operational requirements for successful study implementation.
  • Minimum of 10 years of direct experience with CRO or pharmaceutical data; sourcing, integration, analysis, and reporting.
  • Ability to advise and interact with all levels of staff.
  • Ability to demonstrate excellent analytical skills, exercise sound judgment, and make decisions independently.


At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):

United States of America - $118,500.00 - $234,500.00

The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

About Worldwide Clinical Trials

Worldwide Clinical Trials is a global contract research organization (CRO) that provides clinical research services to pharmaceutical and biotechnology companies. They specialize in early phase development, late phase development, and full-service clinical research. Worldwide Clinical Trials has experience in a wide range of therapeutic areas, including oncology, neuroscience, and infectious diseases. They are committed to providing high-quality, efficient, and cost-effective services to their clients.
Learn more about Worldwide Clinical Trials
Size
1,500 employees
Industry
Founded
1986

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