Associate Director Clinical Operations


Bethesda
Permanent
USD135000 - USD175000
Clinical Development
PR/534288_1740014331
Associate Director Clinical Operations

Associate Director Clinical Operations

Washington D.C. (Hybrid)

$135,000-$175,000

Job Description

EPM is partnered with a leading Contract Research Organization (CRO) dedicated to advancing clinical research and improving patient outcomes. Our partner is renowned for its innovative approach, cutting-edge technology, and commitment to excellence in clinical trials. With a global presence and a diverse portfolio of therapeutic areas, they offer a dynamic and collaborative environment for professionals passionate about making a difference in healthcare. Join a team that values integrity, innovation, and impact, and be part of a mission to transform clinical research.

Key Qualifications

  • Bachelor's degree in Life Sciences, Nursing, or a related field; advanced degree preferred.
  • Minimum of 10 years of experience in clinical operations, with at least 3 years in a leadership role.
  • Proven experience in monitoring and remote data review.
  • Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements.
  • Excellent leadership, communication, and interpersonal skills.
  • Ability to manage multiple projects and priorities in a fast-paced environment.
  • Experience with budget management and resource allocation.
  • Proficiency in clinical trial management systems (CTMS) and other relevant software.

Key Responsibilities:

  • Oversee the planning, execution, and management of clinical trials.
  • Lead and mentor a team of clinical operations professionals.
  • Ensure compliance with GCP, regulatory requirements, and company SOPs.
  • Collaborate with cross-functional teams to achieve project goals.
  • Manage budgets, timelines, and resources effectively.
  • Build and develop a team of CTM's and CRA's to monitor clinical trials
  • Establish Risk-Based Quality Management and Centralized Monitoring processes corporately and for applicable clinical trials.
  • Review protocols to ensure the set-up, review and reporting requirements for KRIs and QTLs can be met and are standardized.
  • Provide technical oversight, guidance and coordination for all the central monitor activities.
  • Perform central monitoring activities including review system outputs, propose suggestions for signal and action management, and follow up with study team for action resolutions.

Benefits

  • Medical
  • Dental
  • Vision
  • PTO

FAQs

Congratulations, we understand that taking the time to apply is a big step. When you apply, your details go directly to the consultant who is sourcing talent. Due to demand, we may not get back to all applicants that have applied. However, we always keep your resume and details on file so when we see similar roles or see skillsets that drive growth in organizations, we will always reach out to discuss opportunities.

Yes. Even if this role isn’t a perfect match, applying allows us to understand your expertise and ambitions, ensuring you're on our radar for the right opportunity when it arises.

We also work in several ways, firstly we advertise our roles available on our site, however, often due to confidentiality we may not post all. We also work with clients who are more focused on skills and understanding what is required to future-proof their business. 

That's why we recommend registering your resume so you can be considered for roles that have yet to be created. 

Yes, we help with CV and interview preparation. From customized support on how to optimize your CV to interview preparation and compensation negotiations, we advocate for you throughout your next career move.

Handpicked roles for you