Worldwide Clinical Trials

Associate eCOA Manager - US - Remote

Worldwide Clinical Trials$71K — $142K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Degree in a relevant discipline or equivalent experience
  • Minimum 1 year in eCOA and clinical trials
  • Minimum 1 year in project management
  • Knowledge of operational aspects of Phase I-IV clinical research
  • Familiarity with Software Development Life Cycle (SDLC) and eCOA topics
  • Fluent in English for day-to-day business communication
  • Ability to travel domestically and internationally for key meetings.

Responsibilities

  • Provide project management oversight for eCOA from maintenance to decommissioning.
  • Review study trends and collaborate with eCOA vendors and study teams.
  • Communicate project activities and serve as escalation point for issues.
  • Coordinate eCOA project communications, including reports and meeting schedules.
  • Review and approve eCOA study design and User Requirements Specification (URS).
  • Prepare, review, and approve site materials and helpdesk documentation.
  • Manage financial reviews and budget, including Change Orders.

Benefits

  • Inclusive and equitable workplace culture
  • Focused on mentorship and training opportunities
  • Transparent compensation practices
  • Emphasis on career growth and internal promotions
  • Supportive team environment with collaborative work culture.
Full Job Description
What the Clinical Systemss Department does at Worldwide

Our Clinical Systems Department plays an essential role for the entire organization by ensuring our systems are developed to study specifications, fully integrated, optimally running, and well-maintained throughout the studies' lifecycle. The department works closely with industry specific systems such as: IRT, RTSM, EDC, RBQM Opra, ClinSpark, eTMF and CTMS. The department has various roles including client-facing Project Managers, System and Software Designers, and Implementation and Validation specialists. Each of these areas provides mentorship and training. In working with a variety of systems, the department has a proven record of success for promotions and growth internally.

What you will do

  • Provide project management oversight from maintenance to eCOA decommissioning, including oversight and accountability of deliverables and timelines and completion of work to Worldwide SOP standards
  • Review and identify study trends and proactively work with eCOA vendor and study team to address study specific requirements
  • Communicate information on applicable eCOA project activities to stakeholders, including internal and sponsor study teams. Serves as the escalation point of contact for all eCOA assigned study-related project issues
  • Overall accountability for coordination and timely delivery of eCOA project communications including study status reports, meeting agendas and minutes and scheduling project calls
  • Responsible for overall eCOA study design review and approving User Requirements Specification (URS) for post go-live Change in Scope
  • Prepare, review and approve site and support materials as well as helpdesk documentation, when required
  • Perform financial review and budget management, including review of Change Orders


What you will bring to the role

  • Proficient client-facing skills
  • Proficient in the use of common office software
  • Self-motivated individual who can positively contribute to a team environment
  • High attention to detail
  • Ability to prioritize and handle multiple projects simultaneously
  • Flexible and able to use sound independent judgment and take initiative to assess information
  • Able to make effective decisions in a fast-paced, highly dynamic environment
  • Able to be creative, adapt to new technologies, concepts and processes, make improvements and solve problems Highly organized, detail- and service-oriented
  • Excellent project management skills


Your experience

  • Educated to degree level in a relevant discipline or able to demonstrate equivalent experience Minimum 1 year of experience working in eCOA and clinical trials Minimum 1 year of experience in project management The individual must demonstrate an ability to lead, understand policies and procedures, financial and leadership principles, possesses excellent time management and project management skills and communicate effectively.
  • Demonstrable knowledge of operational aspects regarding Phase I-IV clinical research trials
  • Has knowledge of the Software Development Life Cycle (SDLC) and be familiar with eCOA topics, including eCOA designs and scales Contract Research Organization (CRO) or pharmaceutical experience required
  • Fluency in English (will be required to write, speak, and understand English to conduct day-to-day business) The role may require travel domestically and internationally in order to attend key meetings. The global nature of the position may also require the incumbent to occasionally manage their time flexibly in order to be responsive to stakeholders in different time zones.


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 - $71,500.00 - $142,500.00

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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