Bedside Data Capture (BDC) Study Designer
Joining Fortrea’s Bedside Data Capture (BDC) team offers an exciting opportunity to contribute to the successful delivery of Phase I clinical studies through innovative electronic data capture solutions. You will work within a highly collaborative, fast-paced environment alongside Clinical Research Units, Biometrics, Clinical Operations, IT teams, and Project Managers to ensure accurate and efficient study setup and execution.
This role is ideal for professionals with experience in clinical research and electronic data capture systems who enjoy translating study protocols into practical data collection solutions. As a BDC Study Configuration Specialist, you will play a critical role in configuring studies, supporting data collection processes, maintaining study documentation, and ensuring the highest standards of quality and compliance throughout the study lifecycle.
What you can expect from us
· Office based or home based in the listed countries
· Rewarding and meaningful work in an established, diverse, highly respected global company
· Highly competitive compensation packages, including country-specific benefits and wellbeing programs
· A genuine work-life balance with flexibility in working arrangements
· Comprehensive onboarding and training supported by experienced colleagues and mentors
· Opportunities for continuous learning, professional development and career progression
Your responsibilities
· Configure studies within the Bedside Data Capture (BDC) system, including recruitment, screening and on-study components, ensuring alignment with study protocols and timelines
· Perform post go-live study updates and system maintenance activities to support ongoing study requirements
· Review and interpret clinical study protocols and translate study design requirements into electronic data collection forms, including both CRF and non-CRF fields
· Collaborate closely with Clinical Operations, Biometrics, Project Managers, CRAs, IT teams and study staff to ensure successful study delivery
· Participate in protocol reviews and provide feedback from a BDC study setup perspective to support efficient study execution
· Support study documentation activities and ensure required documents are available and maintained for inclusion in the electronic Trial Master File (eTMF)
· Ensure compliance with applicable regulatory requirements, GCP, ICH guidelines, SOPs and Good Documentation Practices
· Contribute to internal and external audits, inspections and data requests as required
· Identify study-specific risks, assess their impact and support mitigation activities
· Support User Acceptance Testing (UAT) activities and assist with system validation tasks
Your profile
· Bachelor’s degree in Life Sciences, Clinical Research, Information Technology or another related scientific or technical discipline preferred
· Minimum 3–4 years of experience in a clinical research environment, preferably with exposure to Phase I studies
· Understanding of Electronic Data Capture (EDC) systems and the clinical trial process
· Working knowledge of GCP, ICH Guidelines and 21 CFR Part 11 requirements
· Experience working with clinical source documentation and data collection workflows
· Strong organizational skills with the ability to manage multiple priorities in a deadline-driven environment
· Strong collaboration skills with the ability to work effectively across cross-functional teams
· Experience in a regulated environment and knowledge of medical terminology would be advantageous
· Ability to work independently while maintaining a high level of attention to detail and quality
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit Fortrea.
Fortrea is proud to be an Equal Opportunity Employer.
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on business needs and individual qualifications and do not discriminate based upon race, religion, color, national origin, gender, age, disability, veteran status, genetic information, sexual orientation, gender identity, or any other legally protected characteristic.
For more information about how we collect and store your personal data, please see our Privacy Statement.
If, as a result of a disability, you require a reasonable accommodation to complete your application or participate in the hiring process, please contact [email protected].
Learn more about our EEO & Accommodations request here.
Fortrea is a global contract research organization that provides clinical development services for the life sciences industry. It offers full service, functional service, and hybrid outsourcing models across Phase I–IV trials, clinical pharmacology, and consulting, serving biotech, biopharma, medical devices, and diagnostics. Its work is delivered through a network of investigators and specialized teams in approximately 100 countries, supporting trial design, execution, data management, and regulatory compliance. Fortrea’s approach combines its legacy experience from Covance and Labcorp with a pureplay CRO model to deliver fit-for-purpose solutions and agile project delivery. This positions it to manage trials across more than 20 therapeutic areas with scientific rigor and operational excellence. The company aims to bring predictability to clinical trial execution and help clients turn research ideas into real-world outcomes.
Company Size
10,001+
Company Stage
IPO
Headquarters
Winston-Salem, North Carolina
Founded
2023
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Fortrea and Omico collaboration to advance biomarker-led oncology drug development. GlobeNewswire Published Oct 22, 2026 Collaboration aims to improve trial planning and expand patient access to biomarker-matched studies in Australia Highlights * Collaboration aims to accelerate precision oncology research in Australia * Combines Fortrea's experience in oncology clinical trials with Omico's Precision Oncology Screening Platform Enabling Clinical Trials (PrOSPeCT) program * Together, Fortrea and Omico offer more efficient investigator site selection and faster patient access by connecting patients with relevant biomarker-driven clinical trials Story continues below This advertisement has not loaded yet, but your article continues below. DURHAM, N.C. and SYDNEY, Oct. 22, 2026 (GLOBE NEWSWIRE) - Fortrea (Nasdaq: FTRE) (the "Company"), a leading global contract research organization ("CRO"), and Omico, Australia's leading precision oncology screening and trial matching organization, today announced a collaboration to accelerate precision oncology research by helping connect cancer patients to biomarker-matched clinical trials. By combining Omico's precision oncology network with Fortrea's scientific and clinical trial experience, the joint effort aims to improve study planning, site selection and patient recruitment to expand access to biomarker-driven oncology research globally. Top Stories Interested in more newsletters? Browse here. Through this initiative, Omico will support Fortrea's clients in their oncology drug development needs by providing access to patient population insights, including genomic profiling, trial-matching capabilities, real-world oncology data and patient referral pathways in Australia, a key country both for early and late phase Oncology clinical research activities. The collaboration will combine Fortrea's oncology drug development experience with Omico's flagship Precision Oncology Screening Platform Enabling Clinical Trials (PrOSPeCT) program, the largest cancer genomics initiative in Australia. PrOSPeCT is designed to provide molecular profiling and help match patients to biomarker-driven clinical trials and targeted therapies. Story continues below "Our collaboration with Omico is about seeking to reach the right patient for the right study as quickly as possible," said Oren Cohen, M.D., Chief Medical Officer at Fortrea. "Modern oncology development demands ever-greater precision to match specific cancers with the therapies most likely to benefit patients, and to do so as quickly as possible. Our work with Omico accelerates our ability to identify the right patients for biomarker-driven studies in Australia and help advance precision medicine for people with cancer." Omico has built one of Australia's most extensive precision oncology ecosystems, combining molecular profiling, real-world evidence, cohort research programs and a nationwide network of investigators and clinical sites. Omico has reported more than 23,000 consented patients within its clinic-genomic databases and has received referrals from more than 1,600 clinicians across Australia. "Australia is well positioned to support global biomarker-driven clinical trials, through Omico's established national precision oncology research infrastructure, expertise and networks," said Professor David Thomas, Chief Science and Strategy Officer at Omico. "By combining our national data and trial matching capabilities with Fortrea's global clinical development expertise, we can help international sponsors identify relevant patient populations, plan trials more effectively and support targeted recruitment." This advertisement has not loaded yet. This advertisement has not loaded yet, but your article continues below. Fortrea's oncology expertise is underpinned by thousands of operational professionals and supported by more than 50 oncology physicians on staff. This collaboration comes at a time when modern oncology drug development has accelerated the focus on precision medicine, biomarker-driven development and targeted patient identification. Working together, Fortrea and Omico can offer more efficient site selection and the ability to match patients with appropriate studies tied to their unique genomic data, enabling more people to participate in studies tailored to their specific condition in Australia. About Fortrea Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, biotechnology, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients. Fortrea provides phase I-IV clinical trial management, clinical pharmacology and consulting services. Fortrea's solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in about 100 countries is scaled to deliver focused and agile solutions to clients globally. Learn more about how Fortrea is streamlining drug development at Fortrea.com and follow us on LinkedIn and X and Bluesky. Story continues below This advertisement has not loaded yet, but your article continues below. About Omico Omico is an independent, national, not-for-profit research organisation changing the way we fight cancer. We work to improve outcomes for Australians with cancer by providing equitable access to precision oncology and translating scientific advances into clinical care and research, and generating the evidence needed to inform health policy and system reform. Working with Australia's leading cancer institutes, researchers, clinicians, industry partners, advocacy groups and government, we are accelerating molecular profiling, biomarker-led clinical trials, personalised cancer risk management and real-world evidence. About PrOSPeCT PrOSPeCT is Australia's largest precision oncology initiative. Delivered by Omico and a national network of healthcare, research and industry partners, it provides eligible Australians with access to molecular profiling and matching to biomarker-led clinical trials and therapies (at no cost to the patient), while generating clinical, genomic, treatment and outcomes data to advance research, improve cancer care and inform future health policy. Fortrea Contacts: Galen Wilson (Media) - 703-298-0802, [email protected] Kate Dillon (Media) - 646-818-9115, [email protected] Tracy Krumme (Investors) - 984-385-6707, [email protected] Omico Contact: Kym Bramich (Communications) - +61 414 795 087, [email protected] This advertisement has not loaded yet. Quick Picks
Fortrea completes acquisition of the Early Phase Services division from Worldwide Clinical Trials. Expands Fortrea's early clinical development network with dedicated bioanalytical capabilities, increased clinical research unit capacity and a more integrated platform for clients. Highlights * Fortrea completes acquisition of the Early Phase Services division from Worldwide Clinical Trials * Adds a 60,000-square-foot GLP-compliant bioanalytical laboratory in Austin, Texas; a 200-bed GCP-compliant clinical pharmacology unit in San Antonio, Texas; and a biospecimen storage facility in Pflugerville, Texas * Expands Fortrea's early clinical development capacity to more than 570 beds globally and adds dedicated large and small molecule bioanalytical capabilities * Enables more integrated execution of early-phase studies by reducing operational handoffs between clinical and bioanalytical functions * Strengthens Fortrea's end-to-end clinical development platform supporting clients from first-in-human studies through Phase IV and post-approval evidence generation * Supports Fortrea's growth strategy by scaling early clinical development capabilities, increasing clinical research unit capacity and enhancing the company's ability to create long-term value for shareholders * Provides continuity of operations, study delivery and client support throughout the transition through a strategic alliance agreement between the companies DURHAM, N.C., Oct. 19, 2026 (GLOBE NEWSWIRE) - Fortrea (Nasdaq: FTRE) (the "Company"), a leading global contract research organization ("CRO"), today announced it has completed its acquisition of the Early Phase Services division from Worldwide Clinical Trials. The division consists of a Clinical Research Unit ("CRU") and Bioanalytical Laboratory operations, in an all-cash transaction valued at approximately $45 million. The acquisition strengthens Fortrea's end-to-end clinical development platform by adding a 200-bed Good Clinical Practice-compliant CRU in San Antonio, Texas; a 60,000-square-foot Good Laboratory Practice-compliant bioanalytical laboratory in Austin, Texas; and a biospecimen storage facility in Pflugerville, Texas. Together, these assets expand Fortrea's early-phase capacity to more than 570 beds globally and add in-house large and small molecule bioanalytical capabilities to support clients from first-in-human studies through proof-of-concept and later-stage development. "Completing this acquisition further strengthens our integrated, scalable and scientifically differentiated clinical development platform," said Anshul Thakral, CEO of Fortrea. "This transaction demonstrates tangible progress in Fortrea's return to growth as we invest in our ability to win new opportunities and create lasting value for clients. By bringing together complementary clinical pharmacology and bioanalytical capabilities, we expect to expand the speed, flexibility and talent we can offer clients as they advance increasingly complex development programs. We are pleased to welcome the Early Phase Services team to Fortrea and look forward to delivering a seamless experience for clients, volunteers and the patients we ultimately serve." "With this investment, Fortrea adds capability and capacity in its commitment to help clients design and execute early development programs with greater speed, scientific rigor and operational connectivity," said Scott Dove, Ph.D., president, Clinical Pharmacology Services at Fortrea. "The addition of dedicated bioanalytical capabilities and expanded CRU capacity gives our teams more ways to support both simple and complex studies, streamline execution and generate high-quality data that inform development decisions." The addition of these capabilities complements Fortrea's existing Clinical Pharmacology Services business and broadens its North American CRU footprint. The combined platform is designed to reduce operational handoffs between clinical and bioanalytical functions, improve turnaround times and provide clients with greater flexibility for complex and larger participant studies, broader access to distinct volunteer populations and expanded bedspace capacity across Fortrea's early development network. Fortrea and Worldwide Clinical Trials have also entered into agreements intended to support continuity for clients, employees and ongoing programs. Both organizations remain focused on maintaining project momentum and providing a seamless transition for employees, clients and volunteers. The acquired Early Phase Services operations are now part of Fortrea's Clinical Pharmacology Services business unit. Advisors Barclays served as financial advisor to Fortrea, and Mintz, Levin, Cohn, Ferris, Glovsky and Popeo, P.C. served as its legal counsel. About Fortrea Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development solutions to the life sciences industry. Asianet Pakistan partner with emerging and large biopharmaceutical, biotechnology, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients. Fortrea provides phase I-IV clinical trial management, clinical pharmacology and consulting services. Fortrea's solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Its talented and diverse team working in about 100 countries is scaled to deliver focused and agile solutions to clients globally. Learn more about how Fortrea is streamlining drug development at Fortrea.com and follow Asianet Pakistan on LinkedIn, X and Bluesky. Cautionary Statement Regarding Forward-Looking Statements This press release contains "forward-looking statements" within the meaning of the federal securities laws, including Section 27A of the Securities Act and Section 21E of the Exchange Act. Forward-looking statements by their nature address matters that are, to different degrees, uncertain, such as statements about the anticipated benefits of the transaction, including future financial and operating performance, and the anticipated timing for completing the transaction. In this context, forward-looking statements often address expected future business and financial performance and financial condition, and often contain words such as "guidance," "expect," "assume," "anticipate," "intend," "plan," "forecast," "believe," "seek," "see," "will," "would," "target," similar expressions, and variations or negatives of these words that are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Actual results could differ materially from these forward looking statements due to a number of factors, including, but not limited to: the parties' ability to meet expectations regarding the accounting and tax treatments of the proposed transaction; the anticipated benefits of the acquisition may not be realized, or may be realized more slowly or to a lesser extent than expected, difficulties, delays, costs or disruptions associated with integrating the acquired business, operations, employees, systems and processes into the Company, the ability to retain existing customers and business relationships of the acquired operations and win new business following the acquisition, the ability to retain and integrate key employees of the acquired business, the parties' ability to perform their respective obligations under transition services and other agreements, unanticipated liabilities, expenses or adverse effects associated with the acquired business, the ability to maintain applicable regulatory, quality and accreditation requirements for the acquired sites, and other factors described from time to time in documents that the Company files with the SEC. For a further discussion of the risks relating to the Company's business, see the "Risk Factors" Section of the Company's most recent Annual Report on Form 10-K and subsequent Quarterly Reports on Form 10-Q, as filed with the Securities and Exchange Commission (the "SEC"), as such factors may be amended or updated from time to time in the Company's subsequent periodic and other filings with the SEC, which are accessible on the SEC's website at www.sec.gov. These factors should not be construed as exhaustive and should be read in conjunction with the other cautionary statements that are included or incorporated by reference in this report and in the Company's filings with the SEC. All forward-looking statements are made only as of the date of this report and the Company does not undertake any obligation, other than as may be required by law, to update or revise any forward-looking statements to reflect future events or developments. Fortrea Contacts Galen Wilson (Media) - 703-298-0802, [email protected] Kate Dillon (Media) - 646-818-9115, [email protected] Tracy Krumme (Investors) - 984-385-6707, [email protected] GlobeNewswire Distribution ID 9848525 October 17, 2026 Islamabad:Most parts of the country are expected to experience dry weather over the next twelve hours. According to Radio Pakistan, the northern areas may see partly cloudy skies, with cold conditions anticipated during the morning and night. October 17, 2026 October 16, 2026
Fortrea to participate in September investor conferences. MWN-AI** Summary. Fortrea (Nasdaq: FTRE), a prominent global contract research organization (CRO), has announced its upcoming participation in several key investor conferences in September 2026. Leading this initiative are CEO Anshul Thakral, CFO Jason Knoblauch, and Senior Vice President of Investor Relations Tracy Krumme. The conferences include the Baird 2026 Global Healthcare Conference and Deutsche Bank 2026 Healthcare Summit in New York City, as well as the RBC Pharma Services and Life Science Tools Virtual Conference. On September 15, Fortrea will participate in a fireside chat format at the Baird conference, alongside individual and group meetings, from 2:00 to 2:30 PM EDT. A live webcast of this session will be made available for later access via the Events section of Fortrea's Investor Relations website. The following day, Fortrea will engage in one-on-one and group meetings during the Deutsche Bank summit. Additionally, the company will be involved in similar meeting formats at the RBC virtual conference on September 22. Fortrea stands out as a global leader in providing comprehensive clinical development solutions for the life sciences sector, collaborating with both emerging and established biopharmaceutical, biotechnology, and medical device companies. The organization prides itself on its extensive experience, encompassing over three decades across more than 20 therapeutic areas, and is committed to advancing healthcare innovation that accelerates the delivery of transformative therapies to patients. With a talented workforce of professionals operating in 100 countries, Fortrea is well-equipped to provide agile solutions tailored to global clients. Interested investors and stakeholders can learn more about Fortrea's initiatives and drug development approach by visiting their website and following their updates on social media platforms. MWN-AI** Analysis. As Fortrea (Nasdaq: FTRE) prepares to participate in significant investor conferences throughout September 2026, keen investors should closely monitor the company's developments and performance metrics. With CEO Anshul Thakral and CFO Jason Knoblauch set to engage with investors at the Baird 2026 Global Healthcare Conference and the Deutsche Bank 2026 Healthcare Summit, there's a substantial opportunity for insights into Fortrea's strategic initiatives and operational performance. Fortrea stands out in the contract research organization (CRO) sector, focusing on delivering clinical development solutions to both emerging biopharmaceuticals and established medical firms. The company prides itself on leveraging a rich 30-year history across more than 20 therapeutic areas, indicating robust expertise that investors could view favorably. Additionally, their expansive network of clinical trial sites in over 100 countries ensures comprehensive and agile solutions for clients, positioning Fortrea well amid increasing demand for efficient drug development services. Investors should consider the implications of Fortrea's participation in September conferences for future stock performance. A fireside chat format can often lead to candid communications about the company's pipeline, strategic vision, and market positioning, all of which are key factors influencing investor sentiment. The company's ability to articulate growth prospects and address investor inquiries can potentially lead to increased market confidence. Furthermore, with Fortrea's solutions catering to critical sectors such as biopharmaceuticals and medical devices, the ongoing industry shift towards precision medicine and accelerated drug approvals may provide additional tailwind for Fortrea's growth. Hence, investors might find it prudent to engage with the company's updates and consider investing in FTRE to capitalize on potential upside from upcoming innovations and developments in the healthcare landscape. Engaging with management at these conferences could also yield valuable insights, making outreach critical for investors looking to deepen their understanding of Fortrea's market trajectory. **MWN-AI Summary and Analysis is based on asking OpenAI to summarize and analyze this news release. September 10, 2026 08:58:16 am DURHAM, N.C., Sept. 10, 2026 (GLOBE NEWSWIRE) - Fortrea (Nasdaq: FTRE), a leading global contract research organization ("CRO"), today announced that CEO Anshul Thakral, CFO Jason Knoblauch, and SVP of Investor Relations, Tracy Krumme will participate in the following conferences in September: Baird 2026 Global Healthcare Conference (NYC) Date: Tuesday, September 15, 2026 Format: Fireside Chat & 1x1 and Group Meetings Time: 2:00 -2:30 PM EDT Webcast: FTRE Baird Webcast Deutsche Bank 2026 Healthcare Summit (NYC) Date: Wednesday, September 16, 2026 Format: 1x1 and Group Meetings RBC Pharma Services and Life Science Tools Virtual Conference Date: Tuesday, September 22, 2026 Format: 1x1 and Group Meetings The live webcast and replay of the Baird fireside chat will be accessible through the "Events" section of Fortrea's Investor Relations website. Investors interested in meeting with management should contact their banking representatives. About Fortrea Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development solutions to the life sciences industry. Market Wire News partner with emerging and large biopharmaceutical, biotechnology, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients. Fortrea provides phase I-IV clinical trial management, clinical pharmacology and consulting services. Fortrea's solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Its talented and diverse team working in 100 countries is scaled to deliver focused and agile solutions to clients globally. Learn more about how Fortrea is streamlining drug development at Fortrea.com and follow Market Wire News on LinkedIn, X and Bluesky. Fortrea Contacts Tracy Krumme (Investors) - 984-385-6707, [email protected] Sue Zaranek (Media) - 919-943-5422, [email protected] Kate Dillon (Media) - 646-818-9115, [email protected] FAQ**. What key strategies will Fortrea Holdings Inc. (FTRE) discuss during the Baird 2026 Global Healthcare Conference to showcase their leadership in clinical development solutions? I currently do not have access to specific details about Fortrea Holdings Inc.'s strategies for the Baird 2026 Global Healthcare Conference. Please consult official company announcements or industry news for the latest information. How does Fortrea Holdings Inc. (FTRE) plan to leverage its extensive experience across therapeutic areas during the upcoming Deutsche Bank 20Healthcare Summit? Fortrea Holdings Inc. plans to leverage its extensive experience across therapeutic areas at the Deutsche Bank 2026 Healthcare Summit by showcasing innovative strategies and partnerships that enhance their portfolio and address evolving healthcare needs. What insights does Fortrea Holdings Inc. (FTRE) hope to share with investors at the RBC Pharma Services and Life Science Tools Virtual Conference regarding drug development innovation? Fortrea Holdings Inc. (FTRE) aims to share insights on groundbreaking advancements in drug development and innovative strategies that enhance efficiency and efficacy, positioning their pipeline for growth and competitiveness in the pharmaceutical industry. How is Fortrea Holdings Inc. (FTRE) addressing emerging trends in the biopharmaceutical industry while participating in these September conferences? Fortrea Holdings Inc. (FTRE) is actively engaging at September conferences to showcase its innovative therapies and align with industry trends such as personalized medicine and digital health solutions, highlighting its commitment to advancing biopharmaceutical development. **MWN-AI FAQ is based on asking OpenAI questions about Fortrea Holdings Inc. (NASDAQ: FTRE).
Fortrea's $45M acquisition of Worldwide Clinical Trials' early-phase division adds a 60,000 sq ft bioanalytical lab. Here's what it means for Phase I site…
Fortrea acquires the clinical pharmacology unit and bioanalytical laboratory activities of Worldwide Clinical Trials. This acquisition brings dedicated bioanalytical expertise and increased capacity to Fortrea's early clinical development network as Worldwide continues its strategy to strengthen its clinical development activities, therapeutic leadership, and presence in high-growth markets.