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Precision for Medicine

Global CRO for precision medicine trials

Principal/Senior Clinical Data Scientist

Full-TimeUpdated on 10/23/2026
No salary listed
Expert
Bachelor's
Remote in UK+6 moreMore locations: Remote in Poland | Remote in Slovakia | Remote in Hungary | Remote in Serbia | Remote in Spain | Remote in Romania
RemoteOccasional domestic and international travel, including overnight stays, up to approximately 25%.
Biology & BiotechClinical Research Operations

About the job

Requirements
  • A bachelor's degree or equivalent combination of education and experience in a science or health-related discipline, with proficiency in medical terminology.
  • At least 8 years of clinical research experience, or demonstrated competencies for the position.
  • At least 3 years of oncology experience, including experience within the past 1.5 years.
  • At least 1 year of leadership experience.
  • High proficiency with Microsoft Office products, including Outlook, Word, Excel, PowerPoint, Teams, and OneNote.
  • Professional use of English, both written and oral.
  • Ability to travel domestically and internationally, including overnight stays, up to approximately 25%.
  • Advanced knowledge of oncology and medical terminology, and ability to apply disease assessment criteria, standards of care, and grading criteria to clinical trial data in a clinical research setting.
  • Ability to keep current with medical and indication-specific standards of care, conduct independent research and education, and work remotely while independently leading and supporting work.
  • Scientific curiosity and an investigative mindset, including identifying atypical data patterns, formulating scientific and clinical hypotheses, and driving appropriate follow-up actions.
  • Working knowledge of FDA and ICH-GCP, applicable standard operating procedures and regulatory guidance, the clinical trial process, and clinical research functional departments.
  • Ability to independently manage the Clinical Science operational function in a global, cross-functional environment and escalate appropriately.
  • Ability to plan strategically and apply risk management, time management, negotiation, critical thinking, decision making, listening, analytical, and conflict management skills.
  • Ability to adjust to multiple demands and shifting priorities.
  • Ability to mentor, coach, and develop junior team members while fostering a collaborative learning environment.
  • Ability to apply financial management skills at the functional-area project level.
  • Strong presentation, verbal, and written communication skills.
Responsibilities
  • Lead the Clinical Science function on assigned projects, implementing services according to the study scope of work from study start through database lock and delivering high-quality outcomes within agreed timelines and budgets.
  • Conduct holistic individual and aggregate participant data reviews using proprietary and non-proprietary data review tools and platforms, applying therapeutic-area and indication-specific clinical judgment to support data capture, review and interpretation, query management, and clinically relevant data cleaning.
  • Serve as the scientific and clinical data subject matter expert for study teams, guiding electronic case report form design, data capture requirements, edit checks, completion guidelines, electronic data capture user acceptance testing, and ongoing clinical data review and cleaning to ensure protocol-compliant, high-quality data.
  • Support risk-based quality management by identifying and addressing study risks, trends, and issues, and partnering with cross-functional teams in risk review processes and meetings.
  • Collaborate with Medical Monitoring, including oversight of Medical Monitor review of participant data and data review findings.
  • Review protocols from a scientific operational perspective.
  • Apply working knowledge of oncology and clinical research criteria, including CTCAE, ASTCT, RECIST 1.1, Lugano, and ICANS.
  • Support project and financial management, invoicing, and out-of-scope management.
  • Collaborate with Clinical Science management on resource needs.
  • Oversee or develop and maintain Clinical Science project plans, guidelines, trackers, and programming specifications for data review tools and outputs.
  • Ensure applicable electronic trial master file documentation for Clinical Science is maintained accurately.
  • Participate in internal and external study-specific meetings and presentations, including facilitating, coordinating, and managing Medical Data Review Meetings.
  • Contribute to study-level strategy, data review processes, and continuous improvement initiatives.
  • Support business development, including attending and presenting at bid defense meetings.
  • May review tables, figures, and listings and/or clinical study reports.
Desired Qualifications
  • A medical-related degree or credentials such as registered nurse, oncology certified nurse, registered pharmacist, or Doctor of Pharmacy.
  • Experience with electronic data capture systems.
  • Database build experience.
  • On-site experience as a nurse or study coordinator, monitoring experience, and/or data review experience.
  • Experience with data visualization platforms or software used as data review tools.
  • Experience in Phase I, II, and III studies and global studies.

About the company

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Precision for Medicine

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Precision For Medicine is a global clinical research organization (CRO) that helps life sciences companies run clinical trials from early to regulatory approval. It specializes in precision medicine, focusing on oncology, cell and gene therapy, and rare diseases. The company combines clinical trial services with specialty laboratory work and data sciences to improve speed, reduce costs, and increase the likelihood of success in bringing therapies to patients. It differentiates itself by integrating advanced technologies and data-driven biostatistics with specialized labs to support end-to-end trials across all stages. Its goal is to enable faster, more cost-efficient development of targeted therapies that meet regulatory requirements and reach patients in need.

Company Size

1,001-5,000

Company Stage

Growth Equity (Venture Capital)

Total Funding

$225M

Headquarters

Bethesda, Maryland

Founded

2012

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Simplify Jobs

Simplify's Take

What believers are saying

  • McKesson signed a $2.25 billion acquisition on August 25, 2026, validating Precision's assets.
  • Japan office opened March 11, 2026, improving access to Japan's pivotal-trial market.
  • Amanda Owens and Chris Clendening joined in 2026, signaling biospecimen and lab growth.

What critics are saying

  • McKesson's August 25, 2026 deal can delay decisions until closing approvals finish.
  • Integration with McKesson threatens autonomy; Oncology & Multispecialty will dictate priorities and budgets.
  • A failed McKesson closing becomes existential, risking talent flight and sponsor defections.

What makes Precision for Medicine unique

  • Precision for Medicine pairs CRO execution with specialty labs and biomarker analytics across 40 locations.
  • Oncology dominates: 76% of trials, plus 23 FDA and EMA approvals in ten years.
  • Three former FDA oncology leaders, including Paz Vellanki and Harpreet Singh, sharpen regulatory strategy.

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Benefits

  • Health Insurance
  • Life Insurance
  • Disability Insurance
  • Parental Leave
  • Paid Sick Leave
  • Paid Vacation

Growth & Insights and Company News

6 month growth

0%

1 year growth

1%

2 year growth

3%
PR Newswire
Aug 20th, 2026
Amanda Owens joins Precision for Medicine to expand biospecimen access for drug research

Precision for Medicine has appointed Amanda Owens as General Manager, Biospecimen Solutions. She will lead the business's commercial and operational strategy as demand grows for deeply annotated biospecimens rich in genetic and molecular data. Owens brings extensive life sciences experience across biospecimen services, genomics, gene editing and advanced therapies. She previously held senior commercial leadership roles at Landmark Bio and Discovery Life Sciences. Precision for Medicine maintains biorepositories containing over one million biofluid specimens and three million tissue specimens. The company integrates clinical trial design and execution with laboratory expertise and data intelligence. Owens holds an MBA from the University of Alabama in Huntsville and advanced degrees in biological sciences. She is based in Nashville, Tennessee.

Investors Hangout
Aug 20th, 2026
Amanda Owens leads Precision Medicine's biospecimen expansion.

Amanda Owens leads Precision Medicine's biospecimen expansion. Shaking up the biospecimen game. Amanda Owens, a seasoned pro in the life sciences sector, is now in the driver's seat at Precision for Medicine, taking charge as General Manager of Biospecimen Solutions. This ain't just a fancy title; she's stepping into a role that's shaking up how biopharma taps into biospecimens for drug development. It's a bustling field, folks, because the demands are soaring - everyone wants more data, more accuracy, and more bang for their buck in research. The new frontier in drug development. What's the big fuss about biospecimens, you ask? Well, they're not your average samples snagged off a shelf. Investors Hangout, LLC is talking about specimens that pack a punch with genetic and molecular profiles, the very things pushing forward next-gen therapies. This is a scientific gold rush, and Owens is the guide who knows where to dig. Her track record spans from landmark roles at Discovery Life Sciences to steering commercial ships at Landmark Bio. If there's one thing this industry needs, it's someone who knows how to marry science with strategy - precisely what Owens brings to the table. Unpacking the leadship strategy. Owens steers toward strategic partnerships. If you think it's all about the samples, think again. Sofia Baig, the president over at Precision for Medicine, made it clear: matching the right sample to the right project is an art, not a mere transaction. That means diving deep into what the sponsors need and predicting how those needs morph over time. Precision has these massive stash houses of over a million biofluid specimens and three million tissue samples, so Owens gets to play with a helluva repertoire. "Quality and speed are not negotiable. It's about a comprehensive understanding," said Owens, emphasizing the teardown of transactional barriers. Consultative partnerships over transactions. This isn't just delivering goods. Precision's suite of lab capabilities enables them to dig plenty deeper than the surface level, crafting partnerships instead of simple hand-offs. It's a pivot toward consultative relationships rather than mere supplier-buyer exchanges. This is where the biz smarts meet scientific vigor, and Owens is poised to harness those dual strengths. The broader impact. Why investors should take notice. Here's the investor angle: what Owens' appointment means for the sector is a steady trajectory towards more integrated, technically sophisticated biospecimen solutions. It's a nod toward adding value in the pipeline - accelerating drug discovery translates into quicker revenue streams and perhaps lucrative partnerships or buyouts down the road. Stay tuned to the playbook Owens rolls out because it could be a game-changer in how the industry views biospecimen sourcing. Precision for Medicine's backing, with over 3,500 people spread internationally, serves as both an engine and a shield. Whether you're looking from the perspective of a startup in biotech or a solid player in pharma, these are the kinds of developments that shape strategic pivots and can push market momentum. Play your cards right, and Owens' blueprint might just become the one everyone else tries to imitate. Investors ought to watch how this strategic rolodex grows under her leadership.

PR Newswire
Jul 14th, 2026
Laboratory veteran Chris Clendening joins Precision for Medicine to lead global specialty labs

Precision for Medicine has appointed laboratory industry veteran Chris Clendening as General Manager, Labs Translational Sciences. Reporting to President Sofia Baig, Clendening will oversee Precision's global specialty labs business, including operational delivery, growth strategy, and AI-driven approaches to accelerate biomarker research. Clendening most recently served as Senior Vice President of Biotechnology Operations and Product Development at Clario. He previously spent over a decade in executive leadership at PPD Central Labs, where he developed an evolutionary central laboratory platform that earned him the CenterWatch Award for Innovation. In his new role, Clendening will focus on global operational delivery and developing integrated scientific solutions for Precision's clients worldwide. He holds a Bachelor of Science in biology and chemistry from Muskingum University and is based in Cincinnati, Ohio.

PR Newswire
May 21st, 2026
Former FDA oncology leader Paz Vellanki joins Precision for Medicine as third ex-regulator on team

Precision for Medicine has appointed Paz Vellanki, MD, PhD, as Vice President of Clinical Development, Oncology. Dr Vellanki previously served as Associate Director of the Division of Oncology 2 at the FDA, overseeing drug development for lung cancer, head and neck cancer and rare tumours. Her appointment completes a trio of former FDA oncology leaders at the company, joining Chief Medical Officer Harpreet Singh and Vice President Nicholas Richardson. During nearly seven years at the FDA, Dr Vellanki led the technical guidance on circulating tumour DNA for early-stage solid tumours and served on the Project Endpoint Working Group. The biomarker-driven clinical research organisation, part of Precision Medicine Group, operates across 40 locations globally with 3,500 staff.

El Referente
Mar 26th, 2026
RETECH-Madrid Community helps connect innovation with the real needs of the healthcare system.

RETECH-Madrid Community helps connect innovation with the real needs of the healthcare system. We interviewed the co-founders of eB2, best solution in the RETECH-Madrid Community health challenge. eB2 is a health startup that develops tools and solutions for patient care and monitoring using Artificial Intelligence and mobile technologies. eB2 is a platform applied to mental health, certified as a medical device, that allows continuous monitoring of patient behavior and transforms it into objective clinical indicators. The company has been recognized as the best solution for the health challenge defined by the company Precision for Medicine, at the II Innovation Forum of the RETECH-Madrid Community project. The meeting brought together over 50 ecosystem actors including startups, scaleups, and leading companies in Greentech, Health, and Aerospace at the SID building in Tres Cantos, with the aim of fostering business collaboration and addressing the real challenges of these three strategic sectors through technological solutions. We spoke with Ana Hernando Abascal, co-founder and CEO, and Antonio Artés Rodríguez, co-founder and CSO of Evidence-Based Behavior (eB2) about their startup's goals and their experience in the Digital Entrepreneurship Networks project in the Madrid Community. How would you define your solution in the health field and what needs does it address? eB2 (Evidence-Based Behavior) is an artificial intelligence platform applied to mental health, certified as a medical device, that allows continuous monitoring of patient behavior and transforms it into objective clinical indicators. It addresses a key need of the healthcare system: moving from a reactive model, based on occasional visits, to a preventive model capable of early detection of clinical deterioration. Today, professionals lack continuous and objective tools to anticipate relapses or crises. Our solution acts as a clinical co-pilot, helping professionals make more informed decisions and intervene earlier, improving care quality and system efficiency. Additionally, the platform is also used in clinical and academic research, enabling the generation of scientific evidence and development of new digital biomarkers based on longitudinal data. What does it mean for you to have been selected as the winner among the health startups participating in the II Innovation Forum? It is a very important recognition, especially because it comes from the public-private ecosystem and leading companies in the sector. For us, it validates three things: the relevance of the problem we address, the maturity of our solution, and its real applicability in both clinical and research settings. Furthermore, it represents an opportunity to accelerate collaborations with organizations and advance towards broader implementation in the health system. What are your main business objectives in the short and medium term? In the short term, our goal is to consolidate deployments in hospitals and mental health provider centers and expand the use of the platform in different clinical cases, strengthening impact evidence. We also want to continue promoting its use in clinical and academic research, generating new predictive models and scientific evidence. In the medium term, we aim to scale in Europe, advance in certification as a higher-level medical device, and position ourselves as a standard in mental health monitoring and prediction. What learnings would you highlight from your participation in the innovation forum? The main learning has been the importance of the real fit between problem and solution from the perspective of leading companies. The forum allows rapid validation of what is a priority for the healthcare system: integration, scalability, clinical evidence, and real implementation capacity. I would also highlight the value of the open innovation format, which facilitates very concrete conversations aimed at collaboration in both care and research. What do you consider being part of the startup and innovation ecosystem of the Madrid Community has contributed to you? The Madrid Community has a very strong ecosystem in health, research, and technology, and for us it has been key in our development. eB2 was born as a spin-off from Carlos III University of Madrid, and growing within this environment has allowed us to combine high-level research with real clinical application. Being part of this ecosystem has facilitated collaboration with hospitals, research centers, and other key actors, accelerating both development and clinical and scientific validation of the technology. Additionally, initiatives like RETECH-Madrid Community help connect innovation with real needs of the healthcare system, which is essential for bringing solutions like ours to market. Looking ahead, what milestones or key developments do you expect to achieve? Our next milestones are focused on three areas: First, expanding deployments in health systems and demonstrating impact at large scale. Second, advancing regulatory certification and clinical validation in new use cases. And third, continuing to develop artificial intelligence capabilities and evidence generation through clinical research. Our goal is to contribute to a paradigm shift: a more preventive, personalized, and data-driven mental health. Digital Entrepreneurship Networks. Digital Entrepreneurship Networks in the Madrid Community is a project led by the Madrid Community, through the Ministry of Digitalization, within the framework of the RETECH project (Territorial Networks of Technological Specialization) and funded by European NextGenerationEU funds under the Recovery, Transformation, and Resilience Plan. Investment Guide 2025 National report on tech and innovative companies.