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Search Results Page 3 of 13

Job Locations (All) | US-Remote
Posted Date 1 week ago(6/30/2020 8:36 AM)
Applies a wide range of therapeutic expertise and clinical drug development knowledge to the development of drugs, biologics, devices and/or other products for human use in developing individual clinical study protocols, clinical plan outlines, drug development programs, clinical study reports, manuscripts, investigator brochures, and sections of regulatory submission documents. Also provides therapeutic training to external clients and internal PRA staff.
ID
2020-64416
Job Locations US | US-NC-Raleigh | US-PA-Blue Bell | US-VA-Charlottesville
Posted Date 1 week ago(6/29/2020 8:17 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 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.   **Applicants for this role will need to be flexible to working until 8 pm EST, based on client needs **   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
2020-64405
Job Locations (All) | Canada-BC-Victoria
Posted Date 1 week ago(6/30/2020 9:37 AM)
Who We Are: We Are PRA.  We are 17,000+ employees strong, operating in more than 85+ 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 You Are: You are knowledgeable about work environment conditions and you care about making sure that the office runs smoothly, which includes keeping supplies in stock, working with vendors, meeting support, making sure the facilities are clean, orderly, and safe.  You are a strong communicator and a good listener and you enjoy collaborating with employees to provide excellent customer service. You are detail orientated from ordering the correct type of break and copy room supplies to approving invoices, making sure every detail is right is crucial to your work.  You are analytical and review expenses and question how you can help the company save money and reduce expenses.
ID
2020-64397
Job Locations (All) | US-Remote | Canada-Remote
Posted Date 1 week ago(6/30/2020 9:31 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
2020-64395
Job Locations (All) | US-Remote | Canada-Remote
Posted Date 1 week ago(6/30/2020 11:32 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
2020-64394
Job Locations (All) | US-PA-Blue Bell
Posted Date 1 week ago(6/30/2020 9:24 AM)
Who We Are: 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 You Are:   Study Start Up is your jam! You are flexible, efficient, proactive, and highly motivated.  You are able to  create and re-set priorities in a fast-paced environment without sacrificing your attention to detail.  You work well within a team, both in a leadership role and as a contributor.  You are a confident communicator, don’t take no for an answer, love a challenge, and can independently create solutions to complex issues. The idea of improving the lives of others by using your strategic and interpersonal skills excites you.  Despite a demanding day or difficult discussion, you are able to walk away with your positive attitude  intact.
ID
2020-64391
Job Locations (All) | US-PA-Blue Bell
Posted Date 6 days ago(7/2/2020 5:26 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
2020-64388
Job Locations (All) | US-PA-Blue Bell
Posted Date 6 days ago(7/2/2020 5:25 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
2020-64386
Job Locations (All) | US-PA-Blue Bell
Posted Date 6 days ago(7/2/2020 5:23 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 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
2020-64385
Job Locations (All) | US-Remote
Posted Date 1 week ago(6/29/2020 11:51 PM)
ID
2020-64368
Job Locations (All) | US-Remote | Canada-Remote
Posted Date 1 week ago(6/30/2020 9:17 AM)
  Global Data Manager Strategic Solutions (SSD)    Who we are:   Over 525 PRA Biometrics resources currently in FTE Programs across 12 global clients 86% global team retention (well above industry standard) Resources located in North America, South America, Asia-Pacific 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 Philadelphia headquarters, others at Sponsor sites, global PRA facilities Management almost always grown from within, with a PRA manager in place for every team Teams range in size from 1 resource to 200+ and 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 Have you had a chance to see our sweet office in Blue Bell? Significant return rate of PRA ex-employees Get involved in client initiatives, process improvements, investigator meetings, training, mentoring…..break out of the day-to-day See the results of your work through direct discussions, meetings, townhalls and teambuilding events with client leadership Upward mobility for those that are interested – our SSD leadership structure is primarily built from within and have been in place with us for 5, 10+ years!  High retention of team members and management means stable teams and positive program culture Permanent PRA employees with examples of opportunities to convert to client perm roles Significant global industry conference participation, SCDM, JSM, PhUSE, PharmaSug, DIA.   Overview: Provides data management oversight and accountability for one or more clinical trials.   Responsibilities:   Takes a leadership role with the CRO, the trial customer(s) and other internal and external partners to establish, align and confirm data management expectations for assigned trial(s). With the trial customer, CRO and other functional partners: – Gathers content and integration requirements for eCRF and other data collection tools. – Establishes conventions and quality expectations for clinical data. – Establishes expectations for dataset content and structure. – Set timelines and follow-up regularly to ensure delivery of all Data Management milestones. Performs trial level oversight controls as described in the oversight plan, QC process and work instructions with minimal DML direction. Reviews clinical data management documents (including submission package) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format and consistency. Ensures compliance with regulatory guidelines and the documentation matrix. Ensures real-time inspection readiness of all Data Management deliverables for the trial; Participate in Regulatory Agency and J&J internal audits as necessary. Plans and tracks content, format, quality, and timing of data management deliverables, including, but not limited to, CRF, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival. Ensures deliverables are on time. Takes a leadership role with the assigned clinical working group(s) to ensure that Data Management and TA trial needs and deliverables are met. Identifies and communicates lessons learned, best practices and frequently asked questions at the trial level. Presents and trains at investigator and monitor meetings if needed   Qualifications:   High school diploma with relevant experience required. Bachelor’s degree or equivalent in Health or Science discipline, with experience in clinical research, desired. Minimum of 5 years of Data Management experience (start-up to lock). Clinical trials experience is required. Experience managing multiples studies at once with experience managing competing priorities is needed. Oncology experience is helpful. But, not required. Experience working in highly diverse teams within clinical research; cross-functional, global, multi-regional. Project management skills. Must have prior experience creating timelines and managing deliverables. Vendor management skills. Advanced Microsoft Office skills including the ability to manipulate and analyze data. Must have experience reviewing SAS and SDTM datasets. Experience with RAVE is highly desired. Highly organized with excellent written and verbal communication.  Must have experience presenting during kick-off meetings, investigator meetings, and study team meetings. Ability to interpret clinical trial data and present trends to clinical trial team on data. Very minimal, if any, travel is expected. Possibly for investigator and/or kick-off meetings. To qualify for a role located in the U.S., 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 work visa status.   PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.    
ID
2020-64363
Job Locations (All) | US-Remote | Canada-Remote
Posted Date 6 days ago(7/2/2020 3:05 PM)
  Global Data Manager Strategic Solutions (SSD)    Who we are:   Over 525 PRA Biometrics resources currently in FTE Programs across 12 global clients 86% global team retention (well above industry standard) Resources located in North America, South America, Asia-Pacific 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 Philadelphia headquarters, others at Sponsor sites, global PRA facilities Management almost always grown from within, with a PRA manager in place for every team Teams range in size from 1 resource to 200+ and 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 Have you had a chance to see our sweet office in Blue Bell? Significant return rate of PRA ex-employees Get involved in client initiatives, process improvements, investigator meetings, training, mentoring…..break out of the day-to-day See the results of your work through direct discussions, meetings, townhalls and teambuilding events with client leadership Upward mobility for those that are interested – our SSD leadership structure is primarily built from within and have been in place with us for 5, 10+ years!  High retention of team members and management means stable teams and positive program culture Permanent PRA employees with examples of opportunities to convert to client perm roles Significant global industry conference participation, SCDM, JSM, PhUSE, PharmaSug, DIA.   Overview: Provides data management oversight and accountability for one or more clinical trials.   Responsibilities:   Takes a leadership role with the CRO, the trial customer(s) and other internal and external partners to establish, align and confirm data management expectations for assigned trial(s). With the trial customer, CRO and other functional partners: – Gathers content and integration requirements for eCRF and other data collection tools. – Establishes conventions and quality expectations for clinical data. – Establishes expectations for dataset content and structure. – Set timelines and follow-up regularly to ensure delivery of all Data Management milestones. Performs trial level oversight controls as described in the oversight plan, QC process and work instructions with minimal DML direction. Reviews clinical data management documents (including submission package) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format and consistency. Ensures compliance with regulatory guidelines and the documentation matrix. Ensures real-time inspection readiness of all Data Management deliverables for the trial; Participate in Regulatory Agency and J&J internal audits as necessary. Plans and tracks content, format, quality, and timing of data management deliverables, including, but not limited to, CRF, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival. Ensures deliverables are on time. Takes a leadership role with the assigned clinical working group(s) to ensure that Data Management and TA trial needs and deliverables are met. Identifies and communicates lessons learned, best practices and frequently asked questions at the trial level. Presents and trains at investigator and monitor meetings if needed   Qualifications:   High school diploma with relevant experience required. Bachelor’s degree or equivalent in Health or Science discipline, with experience in clinical research, desired. Minimum of 5 years of Data Management experience (start-up to lock). Clinical trials experience is required. Experience managing multiples studies at once with experience managing competing priorities is needed. Oncology experience is helpful. But, not required. Experience working in highly diverse teams within clinical research; cross-functional, global, multi-regional. Project management skills. Must have prior experience creating timelines and managing deliverables. Vendor management skills. Advanced Microsoft Office skills including the ability to manipulate and analyze data. Must have experience reviewing SAS and SDTM datasets. Experience with RAVE is highly desired. Highly organized with excellent written and verbal communication.  Must have experience presenting during kick-off meetings, investigator meetings, and study team meetings. Ability to interpret clinical trial data and present trends to clinical trial team on data. Very minimal, if any, travel is expected. Possibly for investigator and/or kick-off meetings. To qualify for a role located in the U.S., 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 work visa status.   PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.    
ID
2020-64362
Job Locations (All) | US-Remote | Canada-Remote
Posted Date 1 week ago(7/1/2020 9:42 AM)
Global Data Manager Strategic Solutions (SSD)   Who we are:   Over 525 PRA Biometrics resources currently in FTE Programs across 12 global clients 86% global team retention (well above industry standard) Resources located in North America, South America, Asia-Pacific 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 Philadelphia headquarters, others at Sponsor sites, global PRA facilities Management almost always grown from within, with a PRA manager in place for every team Teams range in size from 1 resource to 200+ and 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 Have you had a chance to see our sweet office in Blue Bell? Significant return rate of PRA ex-employees Get involved in client initiatives, process improvements, investigator meetings, training, mentoring…..break out of the day-to-day See the results of your work through direct discussions, meetings, townhalls and teambuilding events with client leadership Upward mobility for those that are interested – our SSD leadership structure is primarily built from within and have been in place with us for 5, 10+ years!  High retention of team members and management means stable teams and positive program culture Permanent PRA employees with examples of opportunities to convert to client perm roles Significant global industry conference participation, SCDM, JSM, PhUSE, PharmaSug, DIA.   Overview: Provides data management oversight and accountability for one or more clinical trials.   Responsibilities:   Takes a leadership role with the CRO, the trial customer(s) and other internal and external partners to establish, align and confirm data management expectations for assigned trial(s). With the trial customer, CRO and other functional partners: – Gathers content and integration requirements for eCRF and other data collection tools. – Establishes conventions and quality expectations for clinical data. – Establishes expectations for dataset content and structure. – Set timelines and follow-up regularly to ensure delivery of all Data Management milestones. Performs trial level oversight controls as described in the oversight plan, QC process and work instructions with minimal DML direction. Reviews clinical data management documents (including submission package) ensuring appropriate quality, scientific content, organization, clarity, accuracy, format and consistency. Ensures compliance with regulatory guidelines and the documentation matrix. Ensures real-time inspection readiness of all Data Management deliverables for the trial; Participate in Regulatory Agency and J&J internal audits as necessary. Plans and tracks content, format, quality, and timing of data management deliverables, including, but not limited to, CRF, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival. Ensures deliverables are on time. Takes a leadership role with the assigned clinical working group(s) to ensure that Data Management and TA trial needs and deliverables are met. Identifies and communicates lessons learned, best practices and frequently asked questions at the trial level. Presents and trains at investigator and monitor meetings if needed   Qualifications:   High school diploma with relevant experience required. Bachelor’s degree or equivalent in Health or Science discipline, with experience in clinical research, desired. Minimum of 5 years of Data Management experience (start-up to lock). Clinical trials experience is required. Experience managing multiples studies at once with experience managing competing priorities is needed. Oncology experience is helpful. But, not required. Experience working in highly diverse teams within clinical research; cross-functional, global, multi-regional. Project management skills. Must have prior experience creating timelines and managing deliverables. Vendor management skills. Advanced Microsoft Office skills including the ability to manipulate and analyze data. Must have experience reviewing SAS and SDTM datasets. Experience with RAVE is highly desired. Highly organized with excellent written and verbal communication.  Must have experience presenting during kick-off meetings, investigator meetings, and study team meetings. Ability to interpret clinical trial data and present trends to clinical trial team on data. Very minimal, if any, travel is expected. Possibly for investigator and/or kick-off meetings. To qualify for a role located in the U.S., 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 work visa status.   PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.    
ID
2020-64361
Job Locations (All) | US-Remote
Posted Date 7 days ago(7/1/2020 2:38 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 help get life-saving drugs into the hands of those who need them most.  
ID
2020-64358
Job Locations (All) | US-Remote
Posted Date 23 hours ago(7/7/2020 11:29 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.     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.     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
2020-64353
Job Locations (All) | US-Remote
Posted Date 1 week ago(6/29/2020 9:23 AM)
Researches, writes, and edits clinical and regulatory documents by applying functional expertise and clinical drug development knowledge. Writes clear and concise documents, including study reports, protocols, investigator brochures, summary documents, and other scientific documents. Exhibits excellent written and oral communication and presentation skills. Demonstrates technical expertise and background in the use of medical writing templates and software (eg, PleaseReview, Documentum-based platforms, etc.).
ID
2020-64352
Job Locations (All) | US-Remote
Posted Date 6 days ago(7/2/2020 9:07 AM)
Who we are: - Over 525 PRA Biometrics resources currently in FTE Programs across 12 global clients - Resources located in North America, South America, Asia-Pacific 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 Philadelphia headquarters, others at Sponsor sites, global PRA facilities - Management almost always grown from within, with a PRA manager in place for every team - Teams range in size from 1 resource to 200+ and 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 - Have you had a chance to see our sweet office in Blue Bell? - Significant return rate of PRA ex-employees  - Get involved in client initiatives, process improvements, investigator meetings, training, mentoring…..break out of the day-to-day - See the results of your work through direct discussions, meetings, townhalls and teambuilding events with client leadership - Upward mobility for those that are interested – our SSD leadership structure is primarily built from within and have been in place with us for 5, 10+ years!   - High retention of team members and management means stable teams and positive program culture - Permanent PRA employees with examples of opportunities to convert to client perm roles - Significant global industry conference participation, SCDM, JSM, PhUSE, PharmaSug, DIA. 
ID
2020-64341
Job Locations (All) | US-VA-Charlottesville | US-PA-Philadelphia
Posted Date 1 week ago(6/30/2020 9:32 AM)
Who We Are: We Are PRA.  We are 17,000+ employees strong, operating in more than 85+ 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 You Are: You are knowledgeable about work environment conditions and you care about making sure that the office runs smoothly, which includes keeping supplies in stock, working with vendors, meeting support, making sure the facilities are clean, orderly, and safe.  You are a strong communicator and a good listener and you enjoy collaborating with employees to provide excellent customer service. You are detail orientated from ordering the correct type of break and copy room supplies to approving invoices, making sure every detail is right is crucial to your work.  You are analytical and review expenses and question how you can help the company save money and reduce expenses.
ID
2020-64338
Job Locations (All) | US-Remote
Posted Date 2 weeks ago(6/26/2020 1:36 PM)
Who we are: - Over 470 PRA Biometrics resources currently in FTE Programs across 12 global clients - 88% global team retention in 2018 (well above industry standard) - 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 Philadelphia headquarters, others at Sponsor sites, global PRA facilities - Management almost always grown from within, with a PRA manager in place for every team - Teams range in size from 1 resource to 200+ and 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 - Have you had a chance to see our sweet office in Blue Bell? - Significant return rate of PRA ex-employees  - Get involved in client initiatives, process improvements, investigator meetings, training, mentoring…..break out of the day-to-day - See the results of your work through direct discussions, meetings, townhalls and teambuilding events with client leadership - Upward mobility for those that are interested – our SSD leadership structure is primarily built from within and have been in place with us for 5, 10+ years!   - High retention of team members and management means stable teams and positive program culture - Permanent PRA employees with examples of opportunities to convert to client perm roles - Significant global industry conference participation, SCDM, JSM, PhUSE, PharmaSug, DIA.   
ID
2020-64335
Job Locations (All) | US-UT-Salt Lake City
Posted Date 2 weeks ago(6/26/2020 12:51 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 16,000 employees strong, operating in more than 85 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? Are you a recent Medical Assistant Grad looking for experience? Or maybe a skilled CNA, EMT, or Phlebotomist, looking to use your skills in an ever-changing environment? Or, a healthcare professional looking for a career that can impact the lives of millions? Still with me? Good! Then an opportunity as a Medical Research Associate in our Clinical Research Organization is the career for you!
ID
2020-64332

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