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Search Results Page 10 of 12

Job Locations (All) | US-CA-San Francisco | US-CA
Posted Date 1 day ago(7/7/2020 8:42 AM)
HEMATOLOGY-ONCOLOGY CRAS    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.     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, 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
2020-63191
Job Locations (All) | US-TX-Houston | US-TX-Austin | US-TX
Posted Date 6 days ago(7/2/2020 3:06 PM)
  HEMATOLOGY-ONCOLOGY CRAS     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.     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, 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
2020-63189
Job Locations (All) | US-NJ
Posted Date 6 days ago(7/2/2020 3:06 PM)
HEMATOLOGY-ONCOLOGY CRAS   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.   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, 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
2020-63184
Job Locations (All) | US-MA-Boston
Posted Date 7 days ago(7/1/2020 7:17 PM)
Hem-Onc CRAs!   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. 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, 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
2020-63183
Job Locations (All) | US-NY-New York | US-NY
Posted Date 7 days ago(7/1/2020 7:40 PM)
HEM-ONC CRAS!   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. 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, 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
2020-63182
Job Locations (All) | US-PA-Blue Bell
Posted Date 6 days ago(7/2/2020 10:24 AM)
Do you want to be responsible for developing drug supply planning strategy and overall management of supplies for clinical studies?   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.     Who Are You?   You are an experienced professional with a passion for clinical supplies. You are organized, but flexible and adaptable to unexpected changes. You can easily envision the bigger picture, without losing sight of the day-to-day tasks. You can provide excellent leadership to not only your project teams, but also to clients. You are excited and enthusiastic. You motivate your teams to do great work and collaborate easily with your clients. 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
2020-63136
Job Locations (All) | US-CA
Posted Date 3 weeks ago(6/15/2020 8:31 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 are getting life saving drugs into the 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 Director, Clinical Pharmacology, 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
2020-63135
Job Locations (All) | US-Remote
Posted Date 2 months ago(5/12/2020 5:04 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 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 Medical Writer, 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
2020-63134
Job Locations (All) | US-PA-Blue Bell
Posted Date 6 days ago(7/2/2020 10:24 AM)
Do you want to be responsible for developing drug supply planning strategy and overall management of supplies for clinical studies?   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.     Who Are You?   You are an experienced professional with a passion for clinical supplies. You are organized, but flexible and adaptable to unexpected changes. You can easily envision the bigger picture, without losing sight of the day-to-day tasks. You can provide excellent leadership to not only your project teams, but also to clients. You are excited and enthusiastic. You motivate your teams to do great work and collaborate easily with your clients. 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
2020-63133
Job Locations (All) | US-PA | US-NJ
Posted Date 6 days ago(7/2/2020 8:55 AM)
Who we are (PRA's SSD Business Unit) - Over 470 PRA Biometrics resources currently in FTE Programs across 12 global clients - Extremely high 86% of global team retention  - Resources located in North America, South America, China and Europe - Roles include embedded, dedicated leadership structure + all levels of Data Managers, Stats Programmers, Biostatistics, IVRS, ePRO, Medical Coding - Several teams are remote, others partially based in PRA's Philadelphia-area office, others at Sponsor sites, and global PRA facilities - Management is almost always grown from within, with a PRA manager in place for every team - Teams range in size from 1 to 200+ resources - Several relationships have been established for 5, 10, and 15+ years!  Our motto: One client!  One team!  One set of processes to learn!   Why join SSD Biometrics? - PTO policy is very competitive - Employee Stock Purchase Plan - Significant return rate of PRA ex-employees  - Opportunities to get involved in client initiatives, process improvements, investigator meetings, training, mentoring  - See the results of your work through direct discussions, meetings, townhalls and team-building events with client leadership - High retention of team members and management means stable teams and positive program culture We are currently hiring for an experienced ePRO / eCOA Project Manager. This is an excellent opportunity for career development, as our company continues to grow. This particular role will be part of a dedicated Data Management team and support an embedded client, a global Pharmaceutical company.
ID
2020-63086
Job Locations (All) | Canada-Remote | US-Remote
Posted Date 6 days ago(7/2/2020 8:52 AM)
Do you want to watch clinical development change, or be the one to shape it? 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 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 (2020-64064)   Location: Remote (U. S. or Canada)   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. - 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. - Acts as a subject matter expert (SME) for various technologies or processes. Required Qualifications:  - A Bachelor’s degree in Allied Health, Bio-Medical, Clinical Informatics, or a related field. - Ability to work on Eastern Time Zone's hours. - At least 5 years of data management experience. - At least 2 years of experience working for a CRO within the last 5 years.  - Leadership experience, specifically as the primary point of contact for a Clinical Data Management project team. - Lead experience managing at least 3 studies simultaneously. - Oncology and/or Cardiovascular experience. - Expertise in all aspects of the life cycle of a Data Management study and with most of the major tasks involved in each aspect of the study. - Proficiency in at least one Clinical Data Management system. - Budget experience. - Project management experience, including experience managing timelines. - Vendor or third-party management experience. - Proven history of successful interaction with internal and external clients. Preferred Qualifications: - Familiarity with Rave. - Bid defense, local lab, and/or SDTM / Data Programming experience. - Experience working on Oncology and/or Cardiovascular megatrials. For U.S. based applicants to qualify, they must be legally authorized to work in the United States and should not (now or at any future point) require visa sponsorship for employment.    PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans, and individuals with disabilities.  
ID
2020-63077
Job Locations (All) | US-Remote
Posted Date 2 weeks ago(6/25/2020 10:22 AM)
Project Manager – Real World Solutions     The Project Manager/ Senior Project Manager (PM) in Real World Solutions, is responsible for owning and achieving interim and final contractual deliverables for assigned projects/programs, according to time, quality/scope and cost constraints. The PM must have a detailed understanding of all functional service areas and be able to autonomously lead multifaceted functional teams effectively. The candidate is expected to bring to the position a strong understanding for planning and conducting real world research under GEP/GPP and GCP guidelines.
ID
2020-63008
Job Locations (All) | US-Remote | Canada-Remote
Posted Date 2 days ago(7/6/2020 10:21 AM)
  Project Manager – Real World Solutions     The Project Manager/ Senior Project Manager (PM) in Real World Solutions, is responsible for owning and achieving interim and final contractual deliverables for assigned projects/programs, according to time, quality/scope and cost constraints. The PM must have a detailed understanding of all functional service areas and be able to autonomously lead multifaceted functional teams effectively. The candidate is expected to bring to the position a strong understanding for planning and conducting real world research under GEP/GPP and GCP guidelines.
ID
2020-63007
Job Locations (All) | US-WI | US-MN
Posted Date 2 months ago(5/14/2020 9:14 AM)
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
2020-63005
Job Locations (All) | US-PA
Posted Date 2 months ago(5/7/2020 5:28 PM)
Works in partnership with the scientific, business, operational, clinical and technology areas to support the execution of global clinical trials in the area of global clinical supply management.  This includes management of the planning/forecasting, packaging/labeling, distribution and return of clinical supplies for phase 1-IV clinical trials.
ID
2020-62997
Job Locations (All) | US-PA
Posted Date 2 months ago(5/11/2020 1:18 PM)
Oversees end-to-end clinical supply chain activities to support clinical programs. Collaborates with cross-functional stakeholders in defining and executing operational strategy for clinical supply plans to align with program and study milestones.   Identifies operational risks and implements contingency/mitigation plans for clinical supply activities. Provides functional leadership to direct reports, including hiring, training, staff assignments, coaching/mentoring, performance management and professional development.
ID
2020-62995
Job Locations (All) | US-PA
Posted Date 2 months ago(5/7/2020 5:58 PM)
Do you want to be responsible for developing drug supply planning strategy and overall management of supplies for clinical studies.     Who are we? We Are PRA.   We are 18,000+ 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 an experience professional with a passion for clinical supplies. You are organized, but flexible and adaptable to unexpected changes. You can easily envision the bigger picture, without losing sight of the day-to-day tasks. You can provide excellent leadership to not only your project teams, but also to clients. You are excited and enthusiastic. You motivate your teams to do great work and collaborate easily with your clients. 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
2020-62994
Job Locations (All) | US-CA-San Diego
Posted Date 2 weeks ago(6/23/2020 12:45 PM)
Overview We are looking for an experienced and dedicated scrum master to join our growing team. The individual in this role would be responsible for overseeing our software development team and working under the agile methodology. We are seeking a candidate who has proven leadership skills, the ability to think critically and problem-solve, and a track-record of ensuring project milestones and deadlines are met.   The hired candidate must be willing and capable of adapting the Agile methodologies to a growing team and a growing companies where process are changing to adapt to the company growth.  
ID
2020-62983
Job Locations (All) | US-Remote
Posted Date 2 days ago(7/6/2020 10:59 AM)
  Statistical Programmer 2   Overview:  Provides statistical programming support for the implementation of data models and the reporting of clinical trials.
ID
2020-62835
Job Locations (All) | US-Remote
Posted Date 1 month ago(6/8/2020 1:56 PM)
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
2020-62812

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