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Manager of Drug Safety Coordination Center at Pharmaceutical Research Associates, Inc.

Posted in Executive 30+ days ago.

Location: Raleigh, Kansas





Job Description:

Pharmaceutical Research Associates, Inc.

Manager of Drug Safety Coordination Center

US-KS-Lenexa
US-Remote


Job ID: 2021-73995
Type: US-Midwest
# of Openings: 1
Category: Drug Safety

PRA Health Sciences

Overview

Who are we?

We Are PRA.

We are 20,000+ employees strong, operating in more than 90 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most.

Who are you?

You are a leader and mentor with Data Management and Pharmacovigilance services experience.. You have knowledge of Data Management processes, such as data review, query generation, SAE reconciliation. You wouldn’t dream of being anything, but being a hands-on practical manager who wants to support your team.

This position is full time and remote. Proximity to Kansas City office is preferred for occasional meetings.



Responsibilities

Responsibilities

At our office in Lenexa, Kansas, we currently have an outstanding opportunity for a Team Leader/Functional Manager within our Drug Safety Centre. This position is full time and can be office-based or remote.

Lead your team to be the best! As Team Leader/Functional Manager, you will lead a group of Safety Data Coordinators to provide services for Clinical Coding, SAE Reconciliation, and maybe later also Endpoint Adjudication Coordination. You will build the bridge between Drug Safety and Data Management.

The scope of the Manager of Safety Data Coordinators role includes:


  • Guide, lead and develop a cross cultural team of Safety Data Coordinators

  • Identify and implement process improvements and other ways to improve efficiencies

  • Develop, implement, and monitor team profitability, objectives, and metrics

  • Interact with clients and participate in client meetings as necessary to support and maintain new business; provide leadership in the delivery of related services to clients

  • Provide technical oversight of the generation of project plans such as Coding Conventions, and SAE Reconciliation Plans (and potentially Adjudication Coordination plans) in close cooperation with project teams during set-up phase

  • Maintain familiarity with current industry practices and pharmacovigilance regulations

  • Ensure that staff fulfil their responsibilities in accordance with policies, procedures, and SOPs



Qualifications

What's in it for you?

This team is tenured and strong. They are the kindest and most brilliant in the industry and genuinely jump in to help each other. You will work with folks who are passionate about what they do. Leadership and who you report into is important. With this position, it doesn't get any better.

Interested in leading a powerhouse of a team with an incredibly kind heart and equally fierce work ethic? Apply to chat with us.

Qualifications:


    • substantial contract research organization background

    • 1-2 years functional management and/or project leadership experience preferred

    • minimum of 6-7 years’ experience in data management or pharmacovigilance and / or related services, with strong knowledge in either SAE Reconciliation and/or Coding

    • Prefer a Bachelor's degree in Life Sciences

    • Read, write and speak fluent English; fluent in host country language required.

    • Excellent written, oral communication and presentation skills.

    • Skills with industry standard safety or clinical databases.

Location: Lenexa, Kansas or home-based



PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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