Worldwide Clinical Trials

Associate eCOA Manager - US - Remote

Worldwide Clinical Trials$71K — $142K *
US-Anywhere
+ 2 other locationsRemote
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Degree in a relevant discipline or equivalent experience
  • At least 1 year of experience in eCOA and clinical trials
  • Minimum 1 year of project management experience
  • Knowledge of Phase I-IV clinical research trials
  • Familiarity with Software Development Life Cycle (SDLC) and eCOA topics
  • Fluency in English for effective communication
  • Experience in a CRO or pharmaceutical setting is a plus

Responsibilities

  • Manage eCOA projects from maintenance to decommissioning
  • Identify and address study trends in collaboration with vendors and study teams
  • Communicate project activities to stakeholders and serve as escalation point
  • Coordinate and deliver eCOA project communications in a timely manner
  • Approve User Requirements Specification for post-go-live changes
  • Prepare and review site and support materials as needed
  • Perform financial reviews and budget management including change orders

Benefits

  • Commitment to an inclusive and equitable workplace
  • Competitive benefits package based on location
  • Transparent compensation policies
  • Support for internal promotions and growth
  • Opportunities for mentorship and training within the department
Full Job Description
What the ClinicalSystemssDepartment 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, optimallyrunning,and well-maintained throughout the studieslifecycle. The department works closely with industry specific systems such as: IRT, RTSM, EDC, RBQMOpra,ClinSpark,eTMFand CTMS.The department has various roles including client-facing Project Managers, System and Software Designers, and Implementation and Validation specialists.Each of theseareas providesmentorship and training.In working with a variety of systems, the department hasa provenrecordof success for promotions and growth internally.
What you will do
  • Provide project management oversight from maintenance toeCOAdecommissioning, including oversight and accountability of deliverables and timelines and completion of work to Worldwide SOP standards
  • Review andidentifystudy trends and proactively work witheCOAvendor and study team to address study specific requirements
  • Communicate information on applicableeCOAproject activities to stakeholders, including internal and sponsor study teams. Serves as the escalation point of contact for alleCOAassigned study-related project issues
  • Overall accountability for coordination andtimelydelivery ofeCOAproject communications including study status reports, meeting agendas and minutes and scheduling project calls
  • Responsible for overalleCOAstudy design review and approving User Requirements Specification (URS) for post go-live Change in Scope
  • Prepare,reviewand approve site and support materials as well as helpdesk documentation, whenrequired
  • 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 tonew technologies, concepts and processes, makeimprovementsand 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 experienceMinimum 1 yearof experience working ineCOAand clinical trials Minimum 1 year of experience in project management The individual must demonstratean abilityto lead, understand policies and procedures, financial and leadership principles, possesses excellent time management and project management skills and communicate effectively.
  • Demonstrable knowledge of operational aspectsregardingPhase I-IV clinical research trials
  • Has knowledge of the Software Development Life Cycle (SDLC) and be familiar witheCOAtopics, includingeCOAdesigns and scales Contract Research Organization (CRO) or pharmaceutical experiencerequired
  • Fluency in English (will berequiredto write, speak, and understand English to conduct day-to-day business) The role may require travel domestically and internationallyin order toattend key meetings. The global nature of the position may also require the incumbent to occasionally manage their time flexiblyin order tobe 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.

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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