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Search Results Page 7 of 12

Job Locations (All) | US-Remote
Posted Date 2 days ago(7/6/2020 12:31 PM)
We believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you're ready to be a part of something inspiring join us and Discover Your PRA.   Who are we?   We Are PRA.   We are 16,000+ 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.
ID
2020-63980
Job Locations (All) | US-MA-Boston
Posted Date 2 weeks ago(6/23/2020 9:17 AM)
Because we’re hoping you’re here for the latter.   Who are we? We Are PRA.   We are 17,000+ 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 are getting life saving drugs into the of hands those who need them most.   Who are you? You are a forward thinker. You are an innovator that refuses to settle. You want to push the boundaries and change not just what it means to be a Clinical Research Associate Experienced, you want to change the future.  You want to learn from the best, grow your knowledge and your skill set, and you want to build your career here. You want to use the latest technology and tools in the industry to push the momentum of an already growing company forward. You want to find a balance that still lets you be, well, you. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.   Still here? Good. Because if this is you, we’d really like to meet you.
ID
2020-63959
Job Locations (All) | US-MA-Boston
Posted Date 3 weeks ago(6/17/2020 8:27 AM)
  **This is a part time role, Monday through Friday, 8am-12pm with the ability to work outside of these hours as needed.**   PRA is excited to add a part time Office Assistant to our office in Boston, MA.  This role will have a variety of responsibilities including preparing for and hosting client meetings, working with executives to arrange meeting logistics and presentations, greeting visitors, ordering office supplies, and other general administrative tasks. We are looking for an energetic and self-motivated individual that enjoys working with others and has a keen eye for details.
ID
2020-63952
Job Locations (All) | Canada-Remote | US-Remote
Posted Date 6 days ago(7/2/2020 2:54 PM)
  Do you want to watch clinical development change, or do you want to be the one to shape it? Because we’re hoping you’re here for the latter. Who are we? We Are PRA. We are 17,000+ 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.   Senior Principal Biostatistician   Overview: Designs, plans, and executes biostatistical components of clinical trials. Uses sound statistical methodology to conduct studies, prepares the statistical components of protocols, and is responsible for the statistical components of reports.   Responsibilities: - Serves as the lead biostatistician on programs of studies or submissions, or on simple to complex individual studies. - Serves as an independent reporting statistician on data monitoring committees. - Develops statistical analysis plans and reporting specifications for simple to complex clinical studies. - Reviews statistical analyses of other statisticians and interprets results from simple to complex clinical studies. - Performs senior review of TLFs and statistical analysis plans. - Provides significant input in the development and review of CRFs, edit specifications, and critical variable lists. - Performs lead review of TLFs and derived datasets for clinical studies. - Contributes to clinical study protocols and clinical study reports. - Reviews simple to complex randomization specifications and dummy randomization schemes. - Trains and mentors new or junior statisticians on statistical methods and PRA procedures. - Provides statistical training at monthly seminars. - Participates in bid defense meetings.   Qualifications: - Master’s degree in Statistics or Biostatistics is required. PhD is preferred. - Minimum of 5 years of relevant biostatistical experience is required.  - Experience in regulatory submission/interaction is strongly preferred. - Exhibits expertise in multiple statistical areas, the drug development process, SAS procedures, and good programming practices. - Demonstrates ability to plan, supervise, implement, and monitor the statistical processes for multiple clinical trials. - Displays excellent communication skills with demonstrated leadership ability.   PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans, and individuals with disabilities.      
ID
2020-63907
Job Locations (All) | US-Remote
Posted Date 2 weeks ago(6/26/2020 9:12 AM)
  Do you want to watch clinical development change, or do you want to be the one to shape it?   Because we’re hoping you’re here for the latter.   Who are we?   We Are PRA.   We are 17,000+ 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.     Principal Statistical Programmer (6 Month Contract)   Overview: Provides statistical programming support for the implementation of data models and the reporting of clinical trials.  
ID
2020-63906
Job Locations (All) | US-Remote
Posted Date 2 weeks ago(6/23/2020 8:16 AM)
  Do you want to watch clinical development change, or do you want to be the one to shape it?   Because we’re hoping you’re here for the latter.   Who are we?   We Are PRA.   We are 17,000+ 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.     Principal Statistical Programmer (6 Month Contract)   Overview: Provides statistical programming support for the implementation of data models and the reporting of clinical trials.  
ID
2020-63905
Job Locations (All) | US-Remote | Canada-Remote
Posted Date 2 days ago(7/6/2020 12:30 PM)
e believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you're ready to be a part of something inspiring join us and Discover Your PRA.   Who are we?   We Are PRA.   We are 17,000+ 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 are getting life saving drugs into the hands of those who need them most.   Who are you? You are a leader that isn’t afraid to delegate, but also isn’t afraid to get your hands dirty. You look for new and innovative ways to problem solve. You are the ultimate planner and coordinator and are an excellent communicator. You have a serious passion for clinical development. You never settle for what is, but are always pushing clinical development forward to what it could be. You motivate others to do the same. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.   Still here? Good. Because if this is you, we’d really like to meet you. The Study Manager will be accountable for the operational planning, feasibility, and execution of a clinical protocol.
ID
2020-63902
Job Locations (All) | US-Remote | Canada-Remote
Posted Date 2 days ago(7/6/2020 12:29 PM)
We believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you're ready to be a part of something inspiring join us and Discover Your PRA.   Who are we?   We Are PRA.   We are 17,000+ 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 are getting life saving drugs into the hands of those who need them most.   Who are you? You are a leader that isn’t afraid to delegate, but also isn’t afraid to get your hands dirty. You look for new and innovative ways to problem solve. You are the ultimate planner and coordinator and are an excellent communicator. You have a serious passion for clinical development. You never settle for what is, but are always pushing clinical development forward to what it could be. You motivate others to do the same. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.   Still here? Good. Because if this is you, we’d really like to meet you. The Study Manager will be accountable for the operational planning, feasibility, and execution of a clinical protocol.
ID
2020-63901
Job Locations (All) | US-Remote | Canada-Remote
Posted Date 4 weeks ago(6/12/2020 4:46 PM)
We believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you're ready to be a part of something inspiring join us and Discover Your PRA.   Who are we?   We Are PRA.   We are 17,000+ 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 are getting life saving drugs into the hands of those who need them most.   Who are you? You are a leader that isn’t afraid to delegate, but also isn’t afraid to get your hands dirty. You look for new and innovative ways to problem solve. You are the ultimate planner and coordinator and are an excellent communicator. You have a serious passion for clinical development. You never settle for what is, but are always pushing clinical development forward to what it could be. You motivate others to do the same. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.   Still here? Good. Because if this is you, we’d really like to meet you. The Study Manager will be accountable for the operational planning, feasibility, and execution of a clinical protocol.
ID
2020-63900
Job Locations (All) | US-Remote | Canada-Remote
Posted Date 4 weeks ago(6/12/2020 4:44 PM)
We believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you're ready to be a part of something inspiring join us and Discover Your PRA.   Who are we?   We Are PRA.   We are 17,000+ 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 are getting life saving drugs into the hands of those who need them most.   Who are you? You are a leader that isn’t afraid to delegate, but also isn’t afraid to get your hands dirty. You look for new and innovative ways to problem solve. You are the ultimate planner and coordinator and are an excellent communicator. You have a serious passion for clinical development. You never settle for what is, but are always pushing clinical development forward to what it could be. You motivate others to do the same. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.   Still here? Good. Because if this is you, we’d really like to meet you. The Study Manager will be accountable for the operational planning, feasibility, and execution of a clinical protocol.
ID
2020-63899
Job Locations (All) | US-Remote | Canada-Remote
Posted Date 11 hours ago(7/7/2020 10:44 PM)
We believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you're ready to be a part of something inspiring join us and Discover Your PRA.   Who are we?   We Are PRA.   We are 17,000+ 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 are getting life saving drugs into the hands of those who need them most.   Who are you? You are a leader that isn’t afraid to delegate, but also isn’t afraid to get your hands dirty. You look for new and innovative ways to problem solve. You are the ultimate planner and coordinator and are an excellent communicator. You have a serious passion for clinical development. You never settle for what is, but are always pushing clinical development forward to what it could be. You motivate others to do the same. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.   Still here? Good. Because if this is you, we’d really like to meet you. The Study Manager will be accountable for the operational planning, feasibility, and execution of a clinical protocol.
ID
2020-63898
Job Locations (All) | US-NJ | US-PA | US-NY | US-CT
Posted Date 23 hours ago(7/7/2020 11:00 AM)
We believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you're ready to be a part of something inspiring join us and Discover Your PRA.   Who are we?   We Are PRA.   We are 17,000+ 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 are getting life saving drugs into the hands of those who need them most.   Who are you? You are a leader that isn’t afraid to delegate, but also isn’t afraid to get your hands dirty. You look for new and innovative ways to problem solve. You are the ultimate planner and coordinator and are an excellent communicator. You have a serious passion for clinical development. You never settle for what is, but are always pushing clinical development forward to what it could be. You motivate others to do the same. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.   Still here? Good. Because if this is you, we’d really like to meet you. The Study Manager will be accountable for the operational planning, feasibility, and execution of a clinical protocol.
ID
2020-63891
Job Locations (All) | US-Remote
Posted Date 2 days ago(7/6/2020 11:31 AM)
The Senior EDC Programmer is responsible for the development of the Electronic Data Capture (EDC) system and other related departmental systems for the purpose of collecting and reporting clinical study data. The Senior EDC Programmer has thorough knowledge of FDA regulations and industry standards and strong technical skills.
ID
2020-63885
Job Locations (All) | US-FL-Miami | US-FL-Tampa
Posted Date 6 days ago(7/2/2020 3:06 PM)
Calling ALL Experienced Clinical Research Associates – Read On, Join the Movement   We believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you're ready to be a part of something inspiring join us and Discover Your PRA.   Who are we?   We Are PRA.     PRA Health Sciences is seeking the best and brightest, nothing less will do.   We are 17,000+ 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.  When there is a team of 16,000 moving forward together with a common goal, given the support, tools and technology needed, that single step becomes a movement. Interested? Come join the movement and discover YOUR PRA.   What’s in it for you in the long term? - We promote from within – We provide a career not a job. - Culture – There is nothing like it.  We have many former PRA employees returning every single month. - Tools and Technology – Leading the industry with time saving, intuitive smart technology to help predict trends, anticipate needs and eliminate the need for multiple data entry. - Security – We are growing and we are dedicated to having you grow with us. - Mentorship and Training – Our structure provides support for your growth and development as well as questions that arise while on a study at all times. - Work/Life Balance – It's real; we value it. Our strategic solutions and full service models offer you choices for finding a career that includes time for your personal life. - Salary/ Benefits- We are committed to providing our employees with a competitive salary and benefits package with yearly merit and performance reviews.
ID
2020-63884
Job Locations (All) | US-Remote
Posted Date 2 days ago(7/6/2020 12:28 PM)
The Clinical Trial Learning & Development Analyst provides support to CTL&D TA Leads for protocol specific training planning within assigned therapeutic area(s). Service/deliverables include support to deliver on protocol specific training related processes, including, but not limited to development / documentation of the Global Protocol Training Plan (GPTP) for each protocol assigned. Further, services may include project related work, as assigned by TA Lead, and will ensure quality and that work is compliant with company Standard Operating Procedures (SOPs). Partners with the CTL&D TA Leads, EBIS organization and designated study team trial leaders to ensure training plan is documented and implemented in appropriate systems with supporting documentation.
ID
2020-63867
Job Locations (All) | US-Remote
Posted Date 5 days ago(7/3/2020 9:16 AM)
The GCDO Trial Leader (GTL) has primary global accountability at the trial level within the GCDO organization. The GTL is accountable and provides operational expertise for the successful cross-functional delivery of assigned global clinical trial(s), within agreed timelines and budget, and in alignment with all the applicable SOPs and regulatory requirements. The GTL is accountable for oversight of external service providers, planning and execution of both internally managed and outsourced trials, with scope from draft protocol elements document (PED) to availability of the Clinical Study Report (CSR) and applicable disclosure of the trial results. The GTL is responsible for leading the cross-functional Trial Team (including GCDO and non-GCDO members) and interfaces with all trial team members, building the trial operational plan, is responsible for ESP contracts and budget, in alignment with the organizational and the Therapeutic Area (TA) Clinical Team (CT)’s objectives. The GTL provides global operational leadership to the execution to plan and defines risk mitigation strategies and ensures implementation thereof. The GTL maintains oversight of the trial by taking an operational leadership role in a matrix organization, while scientific leadership is provided by the Study Responsible Physician. This includes coordinating activities in the Trial Team and ensuring ad-hoc trial Working Groups are organized as needed, driving issue identification and resolution, contingency planning, and decision-making.
ID
2020-63839
Job Locations (All) | US-Remote
Posted Date 5 days ago(7/3/2020 9:15 AM)
The GCDO Trial Leader (GTL) has primary global accountability at the trial level within the GCDO organization. The GTL is accountable and provides operational expertise for the successful cross-functional delivery of assigned global clinical trial(s), within agreed timelines and budget, and in alignment with all the applicable SOPs and regulatory requirements. The GTL is accountable for oversight of external service providers, planning and execution of both internally managed and outsourced trials, with scope from draft protocol elements document (PED) to availability of the Clinical Study Report (CSR) and applicable disclosure of the trial results. The GTL is responsible for leading the cross-functional Trial Team (including GCDO and non-GCDO members) and interfaces with all trial team members, building the trial operational plan, is responsible for ESP contracts and budget, in alignment with the organizational and the Therapeutic Area (TA) Clinical Team (CT)’s objectives. The GTL provides global operational leadership to the execution to plan and defines risk mitigation strategies and ensures implementation thereof. The GTL maintains oversight of the trial by taking an operational leadership role in a matrix organization, while scientific leadership is provided by the Study Responsible Physician. This includes coordinating activities in the Trial Team and ensuring ad-hoc trial Working Groups are organized as needed, driving issue identification and resolution, contingency planning, and decision-making.
ID
2020-63828
Job Locations (All) | Canada-Remote | US-Remote
Posted Date 6 days ago(7/2/2020 2:54 PM)
  Do you want to watch clinical development change, or do you want to be the one to shape it? Because we’re hoping you’re here for the latter. Who are we? We Are PRA. We are 17,000+ 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.     Senior Lead Data Manager   Overview: Responsible for successfully providing data management deliverables that meet internal and external client needs.   Responsibilities:   - Serves as the primary contact for internal and external team members regarding data management activities. - Authors documents such as interim lock plans, database closure plans, and database unlocking plans. - Tracks milestones, tasks, and the overall budget for assigned projects. - Participates in sponsor and/or third-party audits. - Forecasts units, hours, and resourcing for data management tasks. - Develops plans and oversees timeliness for activities between the last patient visit and the database lock. - Contributes to bid and proposal development and participates in bid defense meetings. - Actively in PRA and data management initiatives. - Responsible for owning and achieving interim and final contractual deliverables for assigned projects. - Ensures quality-control steps are implemented so that quality deliverables are provided. - Mentors and trains other data management team members. - Helps write articles for industry publication and gives presentations at industry conferences. - Strong knowledge of computerized information systems and standard application software (Windows, MS Office). Understands clinical data management systems or electronic data capture software. - Strong understanding of clinical data management and each function as it relates to data management. - Expertise in all aspects of the life cycle of a data management study. - Acts as a subject matter expert (SME) for various technologies or processes.   Qualifications:   - A Bachelor’s degree in Allied Health, Bio-Medical, Clinical Informatics, or a related field is required. - At least 5 years of data management experience is required. - At least 2 years of experience working for a CRO, within the last 5 years, is required.  - Leadership experience, specifically as the primary point of contact for a Clinical Data Management project team. - Lead experience managing at least 3 studies simultaneously. - Experience with all steps within the Data Management lifecycle and most major Data Management study tasks, with proficiency in at least one Clinical Data Management system required. Familiarity with Rave is desired. - Budget experience is required. - Project management experience is required. Must have experience managing timelines. - Vendor management or third-party management experience is required. - Proven history of successful interaction with internal and external clients and an understanding of related functions. - Bid defense experience, local lab experience, SDTM and Data Programming experience desired. But, not required. - Unless otherwise noted, must be able to work from PRA office at least 3 days/week. - For U.S. based applicants to qualify, U.S. applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.   PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans, and individuals with disabilities.  
ID
2020-63812
Job Locations (All) | US-Remote
Posted Date 1 week ago(6/29/2020 1:07 PM)
Who are we? We Are PRA Health Sciences. We provide innovative drug development solutions across all phases and therapeutic areas. But innovation just for the sake of innovation isn’t why we do it. Side by side with our clients, we strive to move drug discovery forward, to help them develop life-saving and life-improving drugs. We help change people’s lives for the better every day. It’s who we are. Innovating to help people is at the heart of our process, but it’s even more than that. It’s our privilege.   We are 17,000+ 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.
ID
2020-63795
Job Locations (All) | US-PA-Blue Bell | US-VA-Charlottesville | US-NC-Raleigh
Posted Date 3 weeks ago(6/18/2020 3:05 PM)
Do you want to watch clinical development change, or do you want to be the one to shape it?     Because we’re hoping you’re here for the latter.   Who are we? We Are PRA.   We are 17,000+ 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 are getting life saving drugs into the hands of those who need them most.   Who are you? You are a forward thinker. Your career trained you to be incredibly thorough and you can track down and document to detail all the relevant facts about an untoward drug effect like a detective. The accuracy and reliability of your work is unquestioned. You are an innovator that refuses to settle. You want to push the boundaries and change not just what it means to be a Senior Drug Safety Associate, you want to change the future. You want to learn from the best, grow your knowledge and your skill set, and you want to build your career here. You want to use the latest technology and tools in the industry to push the momentum of an already growing company forward. You want to find a balance that still lets you be, well, you. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.   Still here? Good. Because if this is you, we’d really like to meet you.   This position will be office based in one of the following offices: Blue Bell, PA; Charlottesville, VA or Raleigh, NC with the flexibility to work from home 1-2 days a week after training and manager approval.  
ID
2020-63794

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