Full-Time

SQL Developer 2

Precision Medicine Group

Precision Medicine Group

1,001-5,000 employees

Biomarker-driven clinical development services and consulting

Compensation Overview

$75k - $95k/yr

+ Discretionary annual bonus

No H1B Sponsorship

Remote in USA

Remote

Bachelor's

Category
Data & Analytics (1)
Required Skills
Microsoft Azure
JavaScript
Microsoft SQL Server
Git
SQL
ETL
.NET
C#
REST APIs
Data Modeling
DevOps
HTML/CSS

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Requirements
  • A bachelor's degree in Computer Science, Information Systems, Mathematics, or a related field, or equivalent experience.
  • Three to five years of experience working with Microsoft SQL Server in a production environment.
  • Hands-on experience writing complex T-SQL queries, stored procedures, functions, views, and data transformations.
  • Experience building and maintaining extract, transform, and load processes and working with large data sets.
  • Proficiency in query optimization, indexing strategies, execution plan analysis, and performance troubleshooting.
  • Experience with data modeling, data validation, data quality checks, and root cause analysis of data defects.
  • Experience with Azure DevOps, Git, continuous integration and continuous delivery concepts, or similar delivery management and source control tools.
  • Accountability for delivering high-quality, accurate work on time.
  • Ability to independently manage multiple priorities and competing deadlines in a fast-paced delivery environment.
  • A detail-oriented, structured approach to problem-solving, documentation, and issue resolution.
Responsibilities
  • Design, develop, and maintain SQL-based data solutions supporting client and product needs.
  • Build and optimize complex queries, stored procedures, functions, views, and database objects for performance and scalability.
  • Develop and maintain extract, transform, and load pipelines to integrate, transform, and validate large data sets.
  • Ensure data accuracy and integrity through validation, reconciliation, and quality checks.
  • Translate business, delivery, and client requirements into technical SQL solutions.
  • Partner with Product Delivery, Client Services, Engineering, and Product teams to deliver client value.
  • Own assigned workstreams, meet deadlines, communicate risks early, and deliver high-quality work with minimal oversight.
  • Create and maintain documentation for data processes, SQL logic, assumptions, and support procedures.
  • Support production systems and resolve data-related issues in a timely manner.
  • Identify and implement process improvements to increase reliability, repeatability, scalability, and efficiency.
  • Participate in code reviews, technical discussions, and delivery planning to improve quality and shared understanding.
  • Apply established standards for change management, data handling, security, documentation, and production readiness.
Desired Qualifications
  • Exposure to application development technologies such as C#, application programming interfaces, .NET, JavaScript, HTML, or front-end frameworks.
  • Excellent communication skills with technical and non-technical stakeholders.
Precision Medicine Group

Precision Medicine Group

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Precision Medicine Group is a life sciences services organization that supports pharmaceutical and biotech companies across the full product lifecycle, from preclinical work to post-launch commercialization. Its offerings are delivered through integrated units like Precision for Medicine and Precision Value & Health, including biomarker assays, cell and gene therapy logistics via Project Farma, global clinical trial management, and regulatory and market-access consulting. The company differentiates itself with an end-to-end, biomarker-centric platform that unites scientific discovery, trial execution, regulatory support, and payer-facing strategy under one umbrella. Its goal is to de-risk and accelerate the development and commercialization of targeted therapies, growing through a mix of organic development and strategic acquisitions.

Company Size

1,001-5,000

Company Stage

Growth Equity (Venture Capital)

Total Funding

$310.2M

Headquarters

Bethesda, Maryland

Founded

2012

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Simplify Jobs

Simplify's Take

What believers are saying

  • 2025-09-16, Tracey Leahy's CPO hire strengthens retention during expansion and integration.
  • 2025-08-08, S&P still expects 10%-11% 2026 revenue growth and stable margins.
  • 2026 M&A interest from buyers supports valuation and validates Precision's service platform.

What critics are saying

  • 2025-08-08, S&P cut leverage to 8.5x-9x after Blackstone's $211 million dividend recap.
  • 2026 sale-review chatter from Blackstone signals ownership instability and potential breakup risk.
  • If pharma spending slows, leveraged CRO margins compress and sponsor-driven exits stall.

What makes Precision Medicine Group unique

  • 2024-10-01, Margaret Keegan replaced founder Mark Clein, signaling institutionalized scaling.
  • Precision for Medicine integrates CRO, biomarkers, labs, and commercialization across one vendor.
  • Epiontis acquisition and Project Farma build rare immune-monitoring and cell-therapy execution depth.

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Benefits

Health Insurance

Life Insurance

Disability Insurance

Parental Leave

Paid Vacation

Paid Sick Leave

Remote Work Options

Performance Bonus

Company News

Daily Dispatch
Jul 21st, 2026
Telix posts strong quarter as revenue nears billion dollar annual run rate.

Telix posts strong quarter as revenue nears billion dollar annual run rate. Telix Pharmaceuticals (ASX:TLX) has reported robust commercial momentum in the quarter ended June 30, 2026, with group revenue of US$247 million, up 21 per cent year over year and 7 per cent from the prior quarter. Precision Medicine led growth with US$202 million in revenue, a 30 per cent increase year over year and 9 per cent sequentially, while Telix Manufacturing Solutions contributed US$45 million. The company said revenue is tracking toward the upper end of its financial year 2026 guidance. It expects revenue and other income to exceed US$1 billion, including a US$40 million non-refundable payment from Regeneron. The company said the quarter featured several regulatory and clinical advances across both the Therapeutics and Precision Medicine portfolios. The United States Food and Drug Administration provided alignment that allows the ProstACT global Phase 3 study of TLX591 Tx to advance to Part 2 in the U.S. Enrollment is progressing in multiple regions, and the program has regulatory approval to commence in China. The OPTIMAL PSMA program completed enrollment in its OPTIMAL PSMA study and has begun dosing in the OPTIMAL-e Phase 2 study for earlier-stage disease. Telix also dosed the first patient in LUTEON, a pivotal trial of TLX250 Tx in clear cell renal cell carcinoma, and enrolled initial cohorts in IPAX BrIGHT, a pivotal trial of TLX101 Tx in recurrent glioblastoma. On the imaging side, Telix reported rapid BiPASS enrollment for Illuccix and Gozellix, and completed patient enrollment in Japan for the registrational study of TLX591 Px with a New Drug Application in preparation. The company said the FDA accepted the resubmitted NDA for Pixclara and granted a PDUFA goal date of September 11, 2026. Telix is also advancing its BLA resubmission for Zircaix and nearing completion of final CMC documentation. Commercial and operational expansion continued with new manufacturing capacity and supply chain investments. Telix recently opened a Telix Manufacturing Solutions (TMS) facility in North Melbourne in partnership with the Melbourne Theranostic Innovation Centre and completed a first GMP production run at TMS Brussels South. The company installed an ARTMS QUANTM irradiation system at TMS Yokohama as part of its plan to scale isotope production globally. Corporate developments during the quarter included a strategic collaboration with Regeneron to jointly develop next-generation radiopharmaceutical therapies and the receipt of an initial US$40 million non-refundable payment. Telix also completed a refinancing by issuing US$600 million of convertible bonds due 2031 and repurchasing its 2029 bonds. Three new non-executive directors joined the board as part of succession planning. Managing Director and Group CEO Dr Christian Behrenbruch said, "We delivered another quarter of growth with U.S. dose volumes increasing 7% during the quarter, driven by growing demand for Gozellix and continued strength across our PSMA imaging portfolio. This performance underscores the strength of our differentiated two-product PSMA imaging strategy and reinforces Telix's market leadership, built on clinical differentiation, supply chain resilience and commercial execution. During the quarter, we achieved key regulatory, commercial and clinical milestones across both our Precision Medicine and Therapeutics businesses. We are tracking in line with the upper end of our FY 2026 revenue guidance and are investing further in R&D to accelerate a number of high-value programs that have the potential to create significant future growth and shareholder value."

SYMEX ECONOMICS SA
Nov 10th, 2025
Lir Life Sciences Corp. Formerly Blackbird Critical Metals Corp. Announces Closing of Acquisition of Lir Life Sciences Inc.

Lir Life Sciences Corp. formerly Blackbird Critical Metals Corp. announces closing of acquisition of Lir Life Sciences Inc. VANCOUVER, BC / ACCESS Newswire / November 10, 2025 / Lir Life Sciences Corp. (CSE:SKNY) (formerly Blackbird Critical Metals Corp.) ("Lir Life Sciences" or the "Company") is pleased to announce, further to its news release dated August 14, 2025, that it has completed the acquisition (the "Transaction") of all of the issued and outstanding shares of Lir Life Sciences Inc. ("Lir Inc."), and that trading in the common shares of the Company resumed on the Canadian Securities Exchange (the "CSE") on November 7, 2025, under the ticker symbol "SKNY". The Company acquired 100% of the issued and outstanding shares of Lir Inc. in consideration for the issuance of 22,312,678 post-consolidated common shares of the Company to the former securityholders of Lir Inc. In connection with the completion of the Acquisition, the Company also issued 379,000 common shares (the "Admin Fee Shares") to The Back Office Inc., an arm's-length third party, as an administrative fee for services rendered in support of the Acquisition. The Admin Fee Shares are subject to a statutory hold period of four months and one day under applicable Canadian securities laws. The Company is pleased to announce that Dr. Edward Mills has been appointed Chief Executive Officer and as a Director of the Company. Dr. Mills is a globally recognized leader in clinical trials and public health, with over 550 peer reviewed publications in top-tier journals such as The New England Journal of Medicine and The Lancet. Over the past two decades, he has led some of the largest and most impactful clinical trials ever conducted, particularly focused on evaluating treatments for diseases affecting low-income populations. His work has earned him multiple prestigious awards in clinical research. Dr. Mills has raised over $1 billion to support clinical research and public health initiatives and is among the most widely published clinical researchers in the world. He holds a PhD in clinical research and two master's degrees. Formerly Chief Executive Officer of Platform Life Sciences and a Senior Scientist at VirX@Stanford, he continues to pioneer breakthrough therapies. He is also a successful entrepreneur, having co-founded and exited several healthcare companies, including MTEK Sciences (acquired by Cytel) and Redwood Outcomes (acquired by Precision Medicine Group). Dr. Mills will lead the Company's vision around the development of therapies intended to provide accessible obesity treatment through transdermal delivery. The Company also welcomes Mr. Harry Nijjar as Chief Financial Officer and Corporate Secretary. Mr. Nijjar is the Managing Director at Malaspina Consultants and a seasoned finance executive with extensive experience in financial reporting, corporate governance, and strategic advisory across a wide range of industries. He serves as Chief Financial Officer for multiple public companies and has held Chief Financial Officer positions with numerous TSX Venture Exchange and CSE listed issuers. Mr. Nijjar earned a Bachelor of Commerce from the Sauder School of Business at the University of British Columbia in 2010 and obtained his CPA, CMA designation in 2012. The Company also welcomes Dr. Mark Dybul as a Director. Dr. Dybul is a Professor in the Department of Medicine at Georgetown University Medical Center where he serves as Chief Strategy Officer of the Center for Global Health Practice and Impact. He is also Chair of the Board of Purpose Africa. Dr. Dybul has worked on HIV and public health for more than 25 years as a clinician, scientist, teacher, and administrator. He was a principal architect of and ultimately led with the rank of Ambassador at the level of an Assistant Secretary of State, the US President's Emergency Plan for AIDS Relief ("PEPFAR"). More recently, he served as the Executive Director of the Global Fund to Fight AIDS, Tuberculosis and Malaria. The Company also welcomes Mr. Kevin May as a Director. Mr. May is an experienced lumber trader with a deep understanding of the North American lumber market, supply chain dynamics, and sustainable forestry practices. With a keen ability to navigate complex trade relationships, he plays a pivotal role in sourcing and distributing high quality timber products to meet the needs of diverse industries. Before transitioning into the lumber trade, Mr. May built a strong foundation in international relations as a cross-cultural communicator in Japan. This experience honed his skills in negotiation, market analysis, and relationship management, the essential qualities that now drive his success in the highly competitive lumber industry. In connection with the Acquisition, and as disclosed by way of news release on October 29, 2025, Lir Inc. completed a non-brokered private placement of 3,050,270 subscription receipts at a price of $0.35 per subscription receipt (the "Concurrent Financing"), for aggregate gross proceeds of $1,067,594.50. Each subscription receipt automatically converted into one common share of Lir Inc. immediately prior to Closing, and such Lir Inc. shares were exchanged for common shares of the Company on closing. Lir Inc. also settled $109,343 of outstanding debt by issuing 312,408 Lir Inc. shares at a deemed price of $0.35 per Lir Inc. share, (the "Debt Conversion") which were exchanged for common shares of the Company on closing. The securities issued in connection with the Concurrent Financing and Debt Conversion are subject to a voluntary hold period of four months from the date from closing. Prior to Closing, on October 31, 2025, the Company effected a change of its corporate name from "Blackbird Critical Metals Corp." to "Lir Life Sciences Corp." (the "Name Change"). For further information regarding the Acquisition, the Concurrent Financing or the Name Change, please see the Listing Statement of the Company dated November 3, 2025, a copy of which is available under the Company's issuer profile on SEDAR+ at www.sedarplus.ca or on the CSE's website. Lir Life Sciences is focused on researching and developing scalable and affordable treatments for obesity using novel drug delivery methods. The company is advancing a transdermal patch and other novel delivery systems that mimic GLP-1, a naturally occurring hormone that helps regulate appetite and blood sugar. These therapies could potentially offer an alternative to injectable drugs. The goal is to improve access, adherence, and cost-efficiency in both developed and emerging markets. LIR Life Sciences aims to address the global burden of obesity with practical solutions based on established compounds and proven science. Neither the CSE nor its Regulation Services Provider accepts responsibility for the adequacy or accuracy of this news release. No stock exchange, securities commission or other regulatory authority has approved or disapproved the information contained herein. This news release contains statements and information that, to the extent that they are not historical fact, may constitute "forward-looking information" within the meaning of applicable securities legislation based on current expectations, estimates, forecasts, projections, beliefs and assumptions made by management of the Company. Forward-looking information is generally identified by words such as "believe", "project", "aim", "expect", "anticipate", "estimate", "intend", "strategy", "future", "opportunity", "plan", "may", "should", "will", "would", and similar expressions and, in this news release, includes statements relating to the commencement of trading of the common shares of the Company, the financial and business prospects of the Company, its assets and other matters. Although the Company believes that the expectations and assumptions on which such forward- looking information are reasonable, undue reliance should not be placed on the forward-looking information because the Company can give no assurance that it will prove to be correct. Since forward-looking information addresses future events and conditions, by its very nature it involves inherent risks and uncertainties. Many factors could cause actual future events to differ materially from the forward-looking information in this news release. The forward-looking information included in this news release is expressly qualified by this cautionary statement. The forward-looking information contained in this news release is made as of the date hereof and the Company undertakes no obligation to update publicly or revise any forward-looking information, whether as a result of new information, future events or otherwise, unless so required by applicable laws.

Precision Medicine Group
Sep 15th, 2025
Precision Medicine Group Announces Appointment of Tracey Leahy as Chief People Officer

BETHESDA, MD., September 16, 2025 - Precision Medicine Group (Precision), a leading provider of next-generation drug development, CRO and commercialization services, today announced the appointment of Tracey Leahy as the company's Chief People Officer (CPO), effective immediately.

Contract Pharma
Apr 16th, 2025
Precision Medicine Group Appoints Chief Information and Technology Officer

Precision Medicine Group, a provider of next-generation drug development, CRO and commercialization services, has appointed Eric Hodgins as its Chief Information and Technology Officer, overseeing all the company's technology assets.

PR Newswire
Oct 2nd, 2024
Precision Medicine Group Welcomes Margaret Keegan as CEO

BETHESDA, Md., Oct. 1, 2024 /PRNewswire/ - Precision Medicine Group (Precision), a leading next-generation provider of drug development and commercialization services, today announced the appointment of Margaret Keegan as Chief Executive Officer (CEO) and member of the Board of Directors, effective immediately.