Providence Medical Technology, Inc. · 10 hours ago
Clinical Scientist
United States
Full-time
Remote
Senior Level
5+ years expProvidence Medical Technology, Inc. is seeking a Clinical Scientist to join their Clinical/Regulatory team. This role involves a hybrid function of Medical Writing, Data Science, and Clinical Data Management, aimed at maximizing the value of clinical, bench, and real-world evidence datasets.
Health CareMedicalMedical Device
Hiring Manager
Anika Nielsen
Responsibilities
Lead strategic analysis and exploration of PMT's clinical datasets to identify insights, claims opportunities, and research pathways
Conduct exploratory analyses on data from the IDE study, legacy clinical studies, real-world evidence programs, and materials/bench testing datasets
Integrate multiple datasets (IDE, post-market, legacy trials, bench data) to explore novel clinical or regulatory claims, identify signals, or highlight areas for further investigation
Develop analytical plans for exploratory work and hypothesis-generative analyses, independently and with consultation/guidance from team and PMT
Identify patterns or early signals that may support future studies, line extensions, product differentiation, or claims expansion
Support cross-functional partners (Regulatory, R&D, Marketing) by translating complex data into actionable narratives or claims opportunities
Generate strategic reports and dashboards summarizing insights, trends, and opportunities discovered through advanced data exploration, and stay abreast of the competition and the clinical evidence factors that provide differentiation in the market
Remain current with regulatory requirements for medical device products
Oversee data integrity, structure, and flow across all PMT studies, with hands-on responsibilities within our bespoke Clinical Trial Management System (CTMS)
Ensure alignment with study protocols and data collection needs
Manage data integrity, in tandem with study management, including eCRF builds, edit checks, user workflows, and quality control steps
Conduct periodic data reviews, resolving inconsistencies and ensuring GCP-compliant data management practices
Develop and deliver interim data summaries and reports to support study conduct, safety monitoring, and internal decision-making
Collaborate with clinical team and contractors, as appropriate, to oversee quality, timelines, and alignment with PMT study priorities
Contribute to data lock, freeze, transfer, and final reporting activities for PMT's new and ongoing clinical studies
Build signal-detection and forecasting tools to help Clinical Affairs anticipate emerging trends or areas of attention as data accrue
Serve as a key driver of PMT's clinical storytelling through high-quality scientific and regulatory writing
Draft, revise, or update key clinical documents, including Clinical Investigation Plans (CIPs) / Study Protocols, ICFs, IBs, protocol amendments and updates, Clinical Study Reports
Develop high-quality scientific content, including abstracts and posters for scientific congresses, peer-reviewed manuscripts for journal submissions, and generate white papers, clinical summaries and value narratives
Support surgeon-authors and key opinion leaders with writing assistance, literature searches, and data interpretation
Ensure consistency, accuracy, and high scientific standards across all written materials
Collaborate cross-functionally to support submissions and evidence packages, as needed
Contribute to publication planning, scientific messaging and dissemination strategy across the organization
Qualification
Required
Advanced degree (Masters or PhD) in a relevant field
Minimum five (5)+ years experience in medical device, clinical research, data analysis and medical writing
Ability/willingness to travel up to 10%
Prior experience with clinical trial protocol development, abstract and manuscript generation
Experience with proprietary or custom data platforms
Experience working in small or mid-sized medical device companies where versatility is essential
Proficient with clinical trial management software
Proficiency with statistical software (R, SAS, Python), even if supported by external partners
Expected subject matter expertise, centering on US Medical Device testing and clinical trials, and their respective regulations, guidance, and policy (i.e., experience with IDE clinical trial and international regulatory process required including FDA (e.g., 21 CFR); ICH and ISO:14155)
Self-motivated, team player, with excellent time management skills to impact a full range of customer, operational, and clinical service activities within the team and cross-functionally
Preferred
Medical device experience in spine and/or implantable device industry strongly preferred
Company
Providence Medical Technology, Inc.
Advancing Cervical Fusion – Providence Medical Technology, Inc.
51-200 employees
H1B Sponsorship
Providence Medical Technology, Inc. has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2024 (1)
2021 (1)
Funding
Current Stage
Late StageTotal Funding
$101.3MKey Investors
Revelation PartnersBridge BankMVM Life Science Partners
2021-01-01Debt Financing· $30M
2018-09-20Series Unknown· $25M
2017-05-10Debt Financing· $10.5M
Leadership Team
Jeff Smith
Chief Executive Officer, Co-founder, Director
Bruce McCormack
Co-Founder, Director
Recent News
2025-02-19
Company data provided by crunchbase