Principal Scientist I, II or III - Purification Chemist - FSP Parexel International CorpPrincipal Scientist I, II or III - Purification Chemist - FSPNJFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. Apply knowledge and skillsets in chromatography, organic chemistry, or biochemistry to execute the purification of API, reaction products, process intermediates, byproducts, or impurities in an R&D laboratory.
Project Leadership - Biotech (clinical trials) - Oncology - Home Based - (Future Needs) Parexel International CorpProject Leadership - Biotech (clinical trials) - Oncology - Home Based - (Future Needs)NCSuccessful candidates possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with at minimum, 2+ years' experience leading Global Clinal Trials in Project Management within a CRO (preferred), Biotech or Pharma company. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.
R0000030967 Senior / Vice President, Technical - Clinical Regulatory Affairs (home-based) Parexel International CorpR0000030967 Senior / Vice President, Technical - Clinical Regulatory Affairs (home-based)MDWe're currently seeking a highly experienced Clinical Regulatory Leader, Health Authority Medical Review Team Lead, Master/Senior Medical Review Officer who is looking to draw upon their wealth of experience in clinical trial design and drug development to join Parexel's highly recognized Regulatory Strategy team! Minimum Work Experience - 15+ years experience with expert level industry or regulatory knowledge experience in Clinical Development/Clinical Trial Design, Clinical Strategy, and authoring clinical sections of regulatory applications.
Clinical Research Nurse / Full time Parexel International CorpClinical Research Nurse / Full timeBaltimore, MD$40–$46 / hourAt Parexel's Baltimore Unit, our highly trained and skilled nurses are the front-line staff involved in administering these new compounds to our volunteer participants via multiple routes, including, but not limited to, IV, IM, SC, PO, Topical, Inhalation etc. Perform or arrange for phlebotomy, urine collection, sample preparation, storage and shipment of samples, drug dispensing, and follows GCP quality study documentation.
Principal Scientist I, II or III - Purification Chemist - FSP Parexel International CorpPrincipal Scientist I, II or III - Purification Chemist - FSPNJFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. Apply knowledge and skillsets in chromatography, organic chemistry, or biochemistry to execute the purification of API, reaction products, process intermediates, byproducts, or impurities in an R&D laboratory.
NewSenior RWE Programmer Parexel International CorpSenior RWE ProgrammerNJExpert Coder: The ideal candidate spends most of their time hands-on coding versus project management or oversight responsibilities, has hands-on experience with raw RWE data including both claims data and Flatiron EHR and can write SQL code from scratch. At least 2-3 years of experience in Real-World Data (RWD) analysis and Real-World Analytics (RWA) using healthcare claims, EMR, and/or registry databases within the biopharmaceutical industry or provider/payer organizations.
Regulatory Affairs Consultant - Clinical Regulatory Affairs Parexel International CorpRegulatory Affairs Consultant - Clinical Regulatory AffairsNCThis highly visible role combines regulatory strategy, global project leadership, health authority engagement, and cross-functional collaboration across programs ranging from early clinical development through registration planning and lifecycle management. Manage and support regulatory submissions and maintenance activities, including IND applications, annual reports, safety submissions, CTA-related activities, protocol amendments, informed consent updates, and end-of-trial deliverables.
Clinical Research Physician (Early Phase Clinical Unit) Parexel International CorpClinical Research Physician (Early Phase Clinical Unit)Baltimore, MDWe are seeking a team-oriented Clinical Research Physician who thrives in a fast-paced, highly specialized research environment and is passionate about mentoring and supporting clinical staff. This role offers the opportunity to contribute to clinical research, collaborate with cross-functional teams and engage directly with sponsors and partners.
Data Quality Lead / Data Management Lead - Oncology Parexel International CorpData Quality Lead / Data Management Lead - OncologyCA$99,000–$180,000 / yearExperience in leading DM study teams, overseeing trial data activities, and collecting clinical trial and/or real-world data, with a good understanding of molecule and disease area strategies and the healthcare environment. Regularly review and update Data Management resources to ensure alignment with contracted budgets, project resource forecasts, actuals, and demand.
Scientist II or III - Metrology Specialist - FSP Parexel International CorpScientist II or III - Metrology Specialist - FSPNJFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. Experience maintaining, operating, and troubleshooting laboratory equipment including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet-Visible spectroscopy (UV-Vis), dissolution systems, and other specialized computerized systems.
Project Leadership - Biotech (clinical trials) -Dermatology - Home Based - (Future Needs) Parexel International CorpProject Leadership - Biotech (clinical trials) -Dermatology - Home Based - (Future Needs)NCSuccessful candidates possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with at minimum, 2+ years' experience leading Global Clinal Trials in Project Management within a CRO (preferred), Biotech or Pharma company. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.
Principal Compliance Consultant - Data Integrity exp is a plus Parexel International CorpPrincipal Compliance Consultant - Data Integrity exp is a plusNCIn contrast to a strictly enforcement-focused role, this position provides the opportunity to work directly with clients to identify risks early, solve complex regulatory challenges, and help organizations achieve and sustain compliance-ultimately impacting product quality and patient outcomes. At Parexel Consulting, former FDA professionals partner with industry to solve complex compliance challenges, guide strategy, and drive meaningful, lasting improvements across global life sciences organizations.
Senior Clinical Research Associate/Clinical Research Associate - All US Locations - FSP Parexel International CorpSenior Clinical Research Associate/Clinical Research Associate - All US Locations - FSPNCFollows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.
Local Study Associate Director- FSP Parexel International CorpLocal Study Associate Director- FSPNCRemoteThe Local Study Associate Director (LSAD) leads Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Client Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations. Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enroll, and in line with Client SOPs.
Senior Regulatory Affairs Consultant (Program / Client Partnership Manager) Parexel International CorpSenior Regulatory Affairs Consultant (Program / Client Partnership Manager)NCYou will play a key leadership role in managing midsize to large Regulatory Affairs outsourcing programs, partnering closely with clients and cross-functional teams to drive operational excellence, ensure delivery against regulatory objectives, and support the successful progression of development and commercial programs. Due to continued growth and the ongoing success of our Regulatory Affairs Consulting team, Parexel is seeking an experienced Senior Regulatory Affairs Consultant (Program / Client Partnership Manager) to join our team.
Executive Director, Site Payment Services Parexel International CorpExecutive Director, Site Payment ServicesNCIf you are you a strategic commercial leader with deep expertise in pricing, partnerships, and the pharmaceutical or CRO (Clinical Research Organization) landscape, join us as an Executive Director, Site Payment Services, where you will play a pivotal role in shaping competitive pricing strategies and driving commercial excellence across a global portfolio. In this highly visible leadership position, you will collaborate with cross-functional teams to influence deal strategy, guide complex bid decisions, and deliver insights that directly impact business growth.
Scientist III - Analytical Chemistry and Molecular Biology - FSP Parexel International CorpScientist III - Analytical Chemistry and Molecular Biology - FSPNJFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. Qualifications - B.S. or M.S. in Chemistry, Chemical Engineering, Biochemistry, Biology or similar life sciences and relevant years of experience in analytical chemistry or biologics testing laboratory: Scientist 3 - B.S. with 3 to 5 years of experience; M.S. with 1 to 2 years of experience.
NewScientist III - Analytical Chemist Drug Product - FSP Parexel International CorpScientist III - Analytical Chemist Drug Product - FSPNJFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. Good organization and project management skills to work on multiple ongoing projects in parallel including routine testing (i.e.- assay/impurity testing) and data processing/interpretation.
Global Clinical Operations Leader / Clinical Trial Manager Parexel International CorpGlobal Clinical Operations Leader / Clinical Trial ManagerRaleigh, NCRemoteWith more than 22,000 employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient focused clinical trials that broaden access and make research a care option for anyone anywhere. You will serve as the primary clinical liaison to project leadership and sponsor teams coordinating cross functional contributors across regions and time zones.
NewDirector, Data Product Coordination Lead (Data & Technology) Parexel International CorpDirector, Data Product Coordination Lead (Data & Technology)NCBuild and develop a team of Data Product Coordinators aligned to specific business domains (Clinical, Corporate, Commercial), ensuring they develop deep domain expertise and act as primary alignment points between business and technical teams. This senior leadership role sits at the center of our data operations, ensuring seamless coordination of data products across business domains and enabling our teams to deliver transformative insights that accelerate clinical research and advance patient care.
NewScientist III - Analytical Chemist Drug Product - FSP Parexel International CorpScientist III - Analytical Chemist Drug Product - FSPNJFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. Good organization and project management skills to work on multiple ongoing projects in parallel including routine testing (i.e.- assay/impurity testing) and data processing/interpretation.
Scientist II or III - Metrology Specialist - FSP Parexel International CorpScientist II or III - Metrology Specialist - FSPNJFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. Experience maintaining, operating, and troubleshooting laboratory equipment including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet-Visible spectroscopy (UV-Vis), dissolution systems, and other specialized computerized systems.
Call Center Agent Parexel International CorpCall Center AgentGlendale, CA$20–$23 / hourHandling incoming and outgoing calls to potential volunteers and closely track daily activity utilizing the Cisco Enterprise Contact Center (automated call distribution system). In addition to base salary, some roles may be eligible for participation in Parexel's annual performance-based bonus plan, annual salary review and additional total rewards incentives.
Senior Clinical Research Associate - Oncology - West Coast - FSP Parexel International CorpSenior Clinical Research Associate - Oncology - West Coast - FSPCAPartner with Site Care Partner to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks. Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File (TMF) documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics.
Site Activation Leader (West Coast Remote) Parexel International CorpSite Activation Leader (West Coast Remote)CORemoteYou will play a critical role in accelerating clinical research by driving efficient site start-up activities from feasibility through activation across multiple studies and therapeutic areas. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Functional Service Provider- Line Manager Parexel International CorpFunctional Service Provider- Line ManagerNCThis may include but not limited to taking the role of a senior level contributor on a project team and ensuring high quality and timely delivery of own deliverables, generating study specific status reports for study teams, Sponsors and/or management, and attend project team meetings as required at the project level. Ensure direct reports meet departmental and project productivity and quality metrics by efficient execution of their project in line with project plan by conducting quality check of deliverables (e.g., on site visits, Central File documentation) and take appropriate remedial action.
Project Leadership - Mid/Large- (clinical trials) - Homebased - (future needs) Parexel International CorpProject Leadership - Mid/Large- (clinical trials) - Homebased - (future needs)NCThe Global Project Leadership department has dedicated members at all levels who are aligned to work with specific types of clients and deliver solutions customized to fit those client's needs, working on projects spanning across all phases of global clinical trials, in a wide array of therapeutic areas. Parexel has upcoming opportunities in a variety of therapeutics at the Project Leader (PM) and Senior Project Leader (SPM) level for candidates with experience leading global studies in a variety of therapeutics supporting mid to large size biotech/ pharma clients.
Senior RWE/RWA Programmer Parexel International CorpSenior RWE/RWA ProgrammerNCAt least 7 years of experience in Real-World Data (RWD) analysis and Real-World Analytics (RWA) using healthcare claims, EMR, and/or registry databases within the biopharmaceutical industry or provider/payer organizations. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Local Study Associate Director - FSP Parexel International CorpLocal Study Associate Director - FSPNCThe Local Study Associate Director (LSAD) leads Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Client Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations. Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enroll, and in line with Client SOPs.
Research Associate (Per Diem Overnight Shift) Parexel International CorpResearch Associate (Per Diem Overnight Shift)Baltimore, MD$20–$22 / hourJob Title: Entry level Research Associate (per diem) Work Location: onsite in Baltimore, MD Parexel Early Phase Clinical Unit supports the development of innovative new medicines which are vital for public health, improving outcomes, and saving lives. Recruit study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments.
Senior Regulatory Consultant - Advertising & Promotion (Strategic Lead) Parexel International CorpSenior Regulatory Consultant - Advertising & Promotion (Strategic Lead)MAAs a result, we are seeking an additional highly strategic and experienced Senior Regulatory Consultant - Advertising & Promotion to serve as a trusted advisor across cross-functional teams on this dedicated client partnership. This role extends beyond execution, requiring a proactive leader who can independently review materials, interpret evolving FDA guidance, and pivot regulatory strategy to support business objectives while mitigating risk.
Scientist II or III - Bioanalytical Sample Management - FSP Parexel International CorpScientist II or III - Bioanalytical Sample Management - FSPPAFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. We are looking to fill a Bioanalytical Sample Management position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in West Point, PA.
Scientist III - Analytical Chemistry and Molecular Biology - FSP Parexel International CorpScientist III - Analytical Chemistry and Molecular Biology - FSPNJFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. Qualifications - B.S. or M.S. in Chemistry, Chemical Engineering, Biochemistry, Biology or similar life sciences and relevant years of experience in analytical chemistry or biologics testing laboratory: Scientist 3 - B.S. with 3 to 5 years of experience; M.S. with 1 to 2 years of experience.
Clinical Supply Support Specialist Services - FSP Parexel International CorpClinical Supply Support Specialist Services - FSPNJFrom clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Clinical Supply Monitoring & Activity Documentation (Electronic Trial Master File - eTMF).
Scientist II or III - Bioanalytical Sample Management - FSP Parexel International CorpScientist II or III - Bioanalytical Sample Management - FSPPAFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. We are looking to fill a Bioanalytical Sample Management position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in West Point, PA.
Clinical Supply Support Specialist Services - FSP Parexel International CorpClinical Supply Support Specialist Services - FSPNJFrom clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Clinical Supply Monitoring & Activity Documentation (Electronic Trial Master File - eTMF).
Per Diem Research Associate (CPT Required) Parexel InternationalPer Diem Research Associate (CPT Required)Glendale, CaliforniaRecruit study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments. Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results.
Associate Counsel Parexel International CorpAssociate CounselRaleigh, NCPreference for 3-6 years' experience in a large multi-national law firm and/or in-house experience supporting commercial operations and negotiating key transactions for a global corporation, ideally in the life sciences. This is a client-facing position, and it is expected that the Associate Counsel will establish highly collaborative, productive relationships with Parexel clients, other business partners and colleagues.
Scientist II or III - Automation Scientist - FSP Parexel International CorpScientist II or III - Automation Scientist - FSPNJFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. These platforms include high-throughput systems from Tecan and Unchained Labs, as well as medium-throughput platforms from Technobis, Mettler Toledo Quantos, Trajan Chronect, and similar systems.
Senior Human Resources Business Partner (Hybrid role in Glendale, CA office) Parexel International CorpSenior Human Resources Business Partner (Hybrid role in Glendale, CA office)Glendale, CA$85,000–$130,000 / yearBy supporting leaders and employees within these specialized units, you'll help strengthen a fast‑paced environment built on scientific insight, quality, and speed as we advance promising therapies through early clinical development. In this role, you will also serve as a key HR partner to our Early Phase clinical units, supporting teams that run first‑in‑human through early patient studies across our global early development network.
Scientist III Microbiologist - FSP Parexel International CorpScientist III Microbiologist - FSPPAFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. We are looking to fill a microbiologist position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients in West Point, PA.
Data Management Lead Parexel International CorpData Management LeadNCThe successful candidate will manage study data delivery timelines, including Go-Live, Interim Deliveries, and Final Database Lock, while working with minimal guidance from Line Managers and/or Subject Matter Experts. This role is responsible for ensuring contracted Data Management deliverables are met with a focus on quality and timeliness, while collaborating closely with cross-functional teams across global geographies.
Financial Analyst III Parexel International CorpFinancial Analyst IIIRaleigh, NCWhat you'll do: Create accurate, transparent, and timely financial analysis to support project leadership in project decision making process; clearly articulate financial implications of business decisions and provide retrospective analysis as well as drive forward looking actions on simpler projects / contract types. Provide updates on financial status for assigned projects and create information in response to any client financial reporting needs for assigned projects in the area of project reporting, forecasting, or transactional details for the projects within the portfolio.
Recruitment Coordinator (Hybrid) Parexel International CorpRecruitment Coordinator (Hybrid)Raleigh, NCResponsibilities include generating candidate correspondence, scheduling interviews, managing applicant tracking systems, and supporting the full recruitment lifecycle with opportunities to deepen your expertise in talent acquisition and influence hiring outcomes. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient‑focused clinical trials that broaden access and make research a care option for anyone, anywhere.
Per Diem Research Associate (CPT Required) Parexel International CorpPer Diem Research Associate (CPT Required)Glendale, CA$20–$26 / hourRecruit study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments. Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results.
Medical Director, Endocrinology Parexel International CorpMedical Director, EndocrinologyCAAs a Medical Director, you will provide medical monitoring for assigned projects, function as medical representative on the project team, provide medical consultation as required or requested to client/sponsor or to other Parexel service groups, and assume the role of Senior Technical Lead in selected circumstances. Review data listings of safety data, including adverse experiences, laboratory data, and vital signs data, to establish the presence or absence of abnormal trends, and if noted, follow up as appropriate with the project team, sponsor, investigator, and FDA.
Recruitment Coordinator - Credentialing (Hybrid) Parexel International CorpRecruitment Coordinator - Credentialing (Hybrid)Raleigh, NCWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. With diverse teams and continuous learning opportunities, the Recruitment Coordinator - Credentialing can explore career paths and expand skills across talent acquisition and human resources.
Project Leadership - Biotech (clinical trials) -Respiratory - Home Based Parexel International CorpProject Leadership - Biotech (clinical trials) -Respiratory - Home BasedNCSuccessful candidates possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with at minimum, 2+ years' experience leading Global Clinal Trials in Project Management within a CRO (preferred), Biotech or Pharma company. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.
Biotech Project Leadership - Clinical Trials - Home- Based - (Future Needs) Parexel International CorpBiotech Project Leadership - Clinical Trials - Home- Based - (Future Needs)NCSuccessful candidates possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with at minimum, 2+ years' experience leading Global Clinal Trials in Project Management within a CRO (preferred), Biotech or Pharma company. Parexel has upcoming opportunities at the Project Leader (PM) and Senior Project Leader (SPM) level for candidates with experience leading global studies in a variety of therapeutics including Neurology, Oncology (Hematology), Respiratory, Cardio, General Medicine and GLP-1 /Obesity.
Project Leadership - Biotech (clinical trials) -Neurology/Psych/Rare Disease - Home Based Parexel International CorpProject Leadership - Biotech (clinical trials) -Neurology/Psych/Rare Disease - Home BasedNCSuccessful candidates possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with at minimum, 2+ years' experience leading Global Clinal Trials in Project Management within a CRO (preferred), Biotech or Pharma company. Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations.