Study Start Up Associate II

3 weeks ago


Reading, Reading, United Kingdom PRA Full time
Study Start Up Associate II

At PRA, we're driven by a shared vision to advance and improve patients' lives. Our diverse teams enable us to become a better partner to our customers and help us to deliver excellence in drug development.

The Role
  • Negotiate and oversee contractual documents and correspondence, ensuring timely execution and compliance with study-specific parameters.
  • Establish and maintain effective communication with study sites, sponsors, and internal personnel regarding budget, contract, and document status.
  • Forecast budget and clinical trial agreement execution timelines, identifying potential risks and developing contingency plans to mitigate impact.
What You Need
  • A bachelor's degree in paralegal studies, juris doctor (law) degree, or related experience is preferred.
  • SSU or contracts experience at a CRO is desired.
  • Experience in a clinical research environment with specific experience in study contracts review and budget negotiation or in a related field.
Benefits of Working at PRA

We offer a competitive salary package, annual bonuses, and a range of health-related benefits to employees and their families. Our inclusive and equal opportunity employer culture values diversity and promotes a workplace free of discrimination and harassment.



  • Reading, Reading, United Kingdom PRA Full time

    Study Start Up Associate IIAt PRA, we're committed to advancing and improving patients' lives through clinical research. Our Study Start Up Associate II plays a vital role in ensuring that physicians at our research sites are prepared to start clinical trials of investigational products.The RoleNegotiate and oversee contractual documents, including CTAs,...


  • Reading, Reading, United Kingdom PRA Full time

    Study Start Up Associate IIAt PRA, we're committed to advancing and improving patients' lives through clinical research. Our Study Start Up Associate II plays a vital role in ensuring that physicians at our research sites are prepared to start clinical trials of investigational products.The RoleNegotiate and oversee contractual documents, including CTAs,...


  • Reading, Reading, United Kingdom PRA Full time

    About the RoleAt PRA, we're committed to advancing human health through innovative clinical research solutions. As a Study Start Up Associate II, you'll play a critical role in ensuring the successful initiation of clinical trials at our research sites.Key ResponsibilitiesNegotiate and manage clinical trial agreements, budgets, and ancillary agreements with...


  • Reading, Reading, United Kingdom PRA Full time

    About the RoleAt PRA, we're committed to advancing human health through innovative clinical research solutions. As a Study Start Up Associate II, you'll play a critical role in ensuring the successful initiation of clinical trials at our research sites.Key ResponsibilitiesNegotiate and manage clinical trial agreements, budgets, and ancillary agreements with...


  • Reading, Reading, United Kingdom PRA Full time

    About the RoleAt PRA, we're committed to advancing human health through our work in clinical research. As a Study Start Up Associate II, you'll play a critical role in ensuring that our research sites are prepared to start clinical trials.Key ResponsibilitiesNegotiate and manage clinical trial agreements, budgets, and ancillary agreements with research sites...


  • Reading, Reading, United Kingdom PRA Full time

    About the RoleAt PRA, we're committed to advancing human health through our work in clinical research. As a Study Start Up Associate II, you'll play a critical role in ensuring that our research sites are prepared to start clinical trials.Key ResponsibilitiesNegotiate and manage clinical trial agreements, budgets, and ancillary agreements with research sites...


  • Reading, Reading, United Kingdom Pharmiweb Full time

    Job Title: Experienced Clinical Research AssociateIQVIA UK is seeking experienced Clinical Research Associates (CRA II / SR CRA I / SR CRA II) to strengthen our cFSP (sponsor-dedicated) team.Key Responsibilities:Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory...


  • Reading, Reading, United Kingdom Pharmiweb Full time

    Job Title: Experienced Clinical Research AssociateIQVIA UK is seeking experienced Clinical Research Associates (CRA II / SR CRA I / SR CRA II) to strengthen our cFSP (sponsor-dedicated) team.Key Responsibilities:Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory...


  • Reading, Reading, United Kingdom ICON plc Full time

    Senior Clinical Research Associate / CRA II - UKAt ICON plc, we're committed to fostering an inclusive environment that drives innovation and excellence in clinical research. We're seeking a Senior Clinical Research Associate and a CRA II to join our dynamic team and contribute to the advancement of innovative treatments and therapies.Key...


  • Reading, Reading, United Kingdom ICON plc Full time

    Senior Clinical Research Associate / CRA II - UKAt ICON plc, we're committed to fostering an inclusive environment that drives innovation and excellence in clinical research. We're seeking a Senior Clinical Research Associate and a CRA II to join our dynamic team and contribute to the advancement of innovative treatments and therapies.Key...


  • Reading, Reading, United Kingdom ICON plc Full time

    Senior Clinical Research Associate / CRA II - UKICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to be part of our mission to shape the future of clinical development.We are currently seeking a Senior Clinical Research...


  • Reading, Reading, United Kingdom ICON plc Full time

    Senior Clinical Research Associate / CRA II - UKICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to be part of our mission to shape the future of clinical development.We are currently seeking a Senior Clinical Research...


  • Reading, Reading, United Kingdom Pharmiweb Full time

    Senior Clinical Research Associate (SR CRA II) Job DescriptionIQVIA UK is seeking a highly skilled Senior Clinical Research Associate (SR CRA II) to join our cFSP team, dedicated to delivering exceptional clinical research services to our clients.Key Responsibilities:Conduct site monitoring visits, ensuring compliance with contracted scope of work and...


  • Reading, Reading, United Kingdom IQVIA, Inc. Full time

    Senior Clinical Research Associate (SR CRA II) Job DescriptionIQVIA UK is seeking a highly skilled Senior Clinical Research Associate (SR CRA II) to join our cFSP team. As a key member of our team, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and ensuring the quality and...


  • Reading, Reading, United Kingdom IQVIA, Inc. Full time

    Senior Clinical Research Associate (SR CRA II) Job DescriptionIQVIA UK is seeking a highly skilled Senior Clinical Research Associate (SR CRA II) to join our cFSP team. As a key member of our team, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and ensuring the quality and...


  • Reading, Reading, United Kingdom IQVIA, Inc. Full time

    Senior Clinical Research Associate (SR CRA II) Job DescriptionIQVIA UK is seeking a highly skilled Senior Clinical Research Associate (SR CRA II) to join our cFSP team. As a key member of our team, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and ensuring the quality and...


  • Reading, Reading, United Kingdom IQVIA, Inc. Full time

    Senior Clinical Research Associate (SR CRA II) Job DescriptionIQVIA UK is seeking a highly skilled Senior Clinical Research Associate (SR CRA II) to join our cFSP team. As a key member of our team, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and ensuring the quality and...


  • Reading, Reading, United Kingdom IQVIA, Inc. Full time

    Senior Clinical Research Associate (SR CRA II) Job DescriptionIQVIA UK is seeking a highly skilled Senior Clinical Research Associate (SR CRA II) to join our cFSP team. As a key member of our team, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and ensuring the quality and...


  • Reading, Reading, United Kingdom IQVIA, Inc. Full time

    Senior Clinical Research Associate (SR CRA II) Job DescriptionIQVIA UK is seeking a highly skilled Senior Clinical Research Associate (SR CRA II) to join our cFSP team. As a key member of our team, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and ensuring the quality and...


  • Reading, Reading, United Kingdom ICON plc Full time

    At ICON plc, we're shaping the future of clinical development by fostering an inclusive environment that drives innovation and excellence. We're seeking a Study Start Up Associate II to join our dynamic team in Madrid, Spain.Key Responsibilities:Lead the preparation and submission of regulatory documents, including clinical trial applications, ethics...