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Recruitment and Screening Coordinator

Employer
Parexel
Location
Harrow, United Kingdom
Salary
Competitive
Start date
8 Oct 2021
Closing date
7 Nov 2021

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Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
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Job Details

Job Description

Role and Responsibilites
  • Coordinate staff and ensuring good communication between both Recruitment and Screening departments.
  • Ensure database records are kept up-to-date, including TOPS entries.
  • Oversee data entry for medical notes.
  • Sending GP reports and chasing outstanding reports to ensure that all data is collected prior to a subject's inclusion.
  • Filing laboratory reports, notifying laboratory if results are missing.
  • Communication with volunteers to ensure that they are kept updated on the progress between screening and inclusion.
  • Responsible for the effective utilization of the volunteer database.
  • Develop and oversee systems to ensure compliance with the Data Protection Act.
  • Ensure sufficient appointments are made to meet the needs of planned/expected screening targets.
  • Review clinical trial protocols for feasibility of recruitment/screening of volunteers as appropriate.
  • Preparation of metrics reflecting recruitment and screening activities.
  • To maintain effective communication with the project managers, nurses and physicians on each project team.
  • Complete tracking and enrolment logs to ensure that screening information is visible for other departments to view.
  • To develop contacts and links with other Phase I Units, in order to maintain subject welfare and prevent'professional volunteers'.
  • Liaise with Line Manager regarding potential efficiencies and improvements within screening/recruitment.
  • Contribute to the maintenance of excellent relationships with members of the public and volunteers to ensure that Parexel is always held in the highest regard.
  • Undertake the full range of duties relevant to the leadership, management and development of the team to ensure their performance meets and or exceeds both the business and their own personal goals/objectives.
  • Maintain a positive, results orientated work environment, building partnerships and modeling teamwork, communicating to the team in an open, balanced and objective manner.
  • Participate in formal staff review processes e.g. performance and salary reviews to corporate standards and timescales.
  • To assist in the conduct of Phase 1 studies across all therapeutic areas in accordance with ICH Good Clinical Practice (GCP) and following local regulatory requirements and relevant Standard Operating Procedures (SOP's).
  • Any other duties as requested by line
    • Qualifications

    Skills and Experience
  • 5 GCSEs, or equivalent as a minimum. Additional qualifications advantageous.
  • Adequate experience of the clinical trials environment.
  • Computer literate.
  • Patient, tolerant and able to cope under pressure.
  • Excellent interpersonal, verbal and written communication skills.
  • Client focused approach to work.
  • A flexible attitude with respect to work assignments and new learning.
  • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.
  • Willingness to work in a matrix environment and to value the importance of teamwork.

    • Apply now to begin your journey!Why Work at Parexel

    There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. What if you had a partner to support you as you reach the next level in your professional path? A partner who believes a collaborative environment is key to achieving your goals? A partner who is dedicated to your health and wellness so you can help make a difference in the lives of millions worldwide?

    That's Parexel. We're a diverse team of professionals focused on one goal: getting treatments into the hands of those who need them most. Working together, the results we bring to our clients and the opportunities we bring to our team get better with every step.

    How can we help you on your journey? Find your path, and learn more on LinkedIn, YouTube, Facebook, Twitter, and Glassdoor.

    Company

    Trialing new treatments. Advancing healthcare. Reinventing medicine as we know it. When you join us, you’re joining a team that sees everything they do as an opportunity to transform the world for patients everywhere. When our employees bring their many perspectives together to tackle a new challenge, there’s no limit to what they can accomplish. Through it all, at the center of all we do, is a patient whose life could change – forever. And together, we’ll do it With Heart™.

    Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help lifesaving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory, and therapeutic expertise, our team of more than 21,000 global professionals works in partnership with biopharmaceutical leaders, emerging innovators, and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. 

    Careers Blog | Our Culture | Diversity, Equity & Inclusion | Benefits | Our Hiring Process

     

    Company info
    Website
    Telephone
    +44 1895 238000
    Location
    The Quays
    101-105 Oxford Road
     Uxbridge
    Middx
    UB8 1LZ
    United Kingdom
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