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Cro Developer Jobs in Minnesota (NOW HIRING)

Partner with space150's engineering and web teams or client-assigned engineering teams to implement ... Help us package and price SEO, GEO, and CRO as sellable services. * Establish the internal ...

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Partner with space150's engineering and web teams or client-assigned engineering teams to implement ... Help us package and price SEO, GEO, and CRO as sellable services. * Establish the internal ...

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Minneapolis, MN 55432 This project will mainly consist of setting up programming code based on the ... IT Life Sciences Allied Healthcare CRO Gold Seal JCAHO Certified for Health Care Staffing "INC 5 0 ...

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Cro Developer information

What is a CRO developer?

A CRO Developer is a specialist who focuses on Conversion Rate Optimization (CRO) for websites and digital products. Their main role is to implement and test changes to web pages—using tools like A/B testing and analytics—to increase the percentage of visitors who complete a desired action, such as making a purchase or filling out a form. CRO Developers work closely with marketing and UX teams to identify pain points in the user journey and apply data-driven solutions. They typically possess skills in front-end development, analytics platforms, and user experience principles. By continuously optimizing websites, CRO Developers help businesses achieve better results from their online traffic.

What are the key skills and qualifications needed to thrive as a CRO developer?

To thrive as a CRO Developer, you need expertise in web development (HTML, CSS, JavaScript), A/B testing methodologies, and a solid understanding of conversion rate optimization principles, often supported by a relevant degree or certification. Familiarity with tools like Google Optimize, Optimizely, VWO, Google Analytics, and tag management systems is typically required. Strong analytical thinking, attention to detail, and effective communication skills help you collaborate with marketing and design teams to drive impactful testing strategies. These skills and qualities are crucial for improving user experience and maximizing website conversion rates, directly impacting business growth.

What are some of the common challenges faced by a CRO developer when optimizing conversion rates across different platforms?

CRO Developers often encounter the challenge of ensuring that conversion optimizations are effective across various devices, browsers, and user segments. Balancing speed of implementation with thorough A/B testing and data analysis can also be demanding, as changes must be both technically sound and data-driven. Additionally, collaborating closely with designers, marketers, and analysts is essential to align technical solutions with broader business goals, which requires strong communication skills and adaptability.

What is the difference between Cro Developer vs Data Analyst?

AspectCro DeveloperData Analyst
Required CredentialsWeb development certifications, knowledge of CRO toolsData analysis certifications, proficiency in SQL and Excel
Work EnvironmentDigital marketing teams, e-commerce companiesBusiness intelligence teams, research firms
Industry UsageOnline retail, SaaS platformsFinance, healthcare, marketing

While Cro Developers focus on optimizing website conversions through A/B testing and user experience improvements, Data Analysts interpret data to inform business decisions. Both roles require analytical skills but serve different functions within digital and data-driven industries.

Is cro in demand?

Conversion Rate Optimization (CRO) specialists are in increasing demand as companies focus on improving website performance and user experience. Skills in data analysis, A/B testing, and tools like Google Optimize or Optimizely are highly valued in digital marketing and e-commerce roles.

Manager, Statistical Programming

Minneapolis, MN • On-site

Linn Products, Inc
201 - 500 employees

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 12 days ago


Job description

Reporting to the Director, Statistical Programming, the Manager, Statistical Programming is responsible for overseeing statistical programming activities for the assigned projects from study planning through database lock, reporting, and regulatory submission. This person provides technical leadership and statistical programming expertise to ensure timely, high-quality, and compliant delivery of clinical trial programming deliverables. The Manager, Statistical Programming is a department-level contributor who collaborates closely with Biostatistics, Clinical Development, Data Management, Regulatory Affairs, Medical Writing, and CRO/vendor partners. The core duties and responsibilities of the Manager, Statistical Programming are delineated below.
Responsibilities:
Department Level
  • Contributes to the development, review, and implementation of departmental SOPs, programming standards, templates, and processes.
  • Supports continuous improvement initiatives to enhance programming quality, efficiency, standardization, and compliance.
  • Contributes to the development and maintenance of reusable programming tools, macros, and automation solutions.
  • Supports resource planning and prioritization across assigned studies and programming activities.
  • Provides technical guidance, mentoring, and knowledge sharing to statistical programmers.
  • Participates in departmental and cross-functional initiatives as appropriate.
  • Contributes to inspection readiness activities and supports departmental responses to programming-related questions or requests

Statistical Programming/Study Tasks
  • Represents Statistical Programming in study team meetings and provides programming input throughout the clinical development lifecycle.
  • Leads and oversees statistical programming activities for assigned clinical studies, including SDTM, ADaM, and Tables, Listings, and Figures (TLFs).
  • Develops, reviews, and/or oversees SAS programs for clinical study deliverables, analysis datasets, and reporting outputs.
  • Reviews and provides input on programming specifications, dataset documentation, validation results, and final deliverables.
  • Ensures statistical programming deliverables are completed according to timelines, quality standards, SOPs, CDISC standards, and regulatory requirements.
  • Supports regulatory submission activities, including preparation and review of SDTM/ADaM datasets, Define-XML, annotated CRF, cSDRG, ADRG, and related submission documentation.
  • Supports clinical publications, abstracts, posters, manuscripts, and external scientific communications through programming deliverables, analysis datasets, tables, listings, and figures.
  • Supports ad hoc analyses, exploratory analyses, and data requests to address clinical development, safety, and business needs.
  • Supports real-world evidence (RWE) initiatives through programming, data preparation, analysis dataset development, and reporting using real-world data sources where applicable.
  • Coordinates and supervise programming activities with CROs and external service providers to ensure quality, consistency, and timely delivery of assigned programming activities.
  • Monitors progress of programming activities and proactively identifies risks, issues, and opportunities for mitigation.
  • Reviews clinical data outputs and programming results to ensure accuracy, completeness, and compliance with specifications.
  • Provides technical support and guidance to resolve complex programming issues.
  • Works independently and collaboratively toward assigned study goals and departmental objectives.

Qualifications:
  • Minimum of eight (8) years of statistical programming experience within the pharmaceutical, biotechnology, CRO, or healthcare industry.
  • Strong proficiency in SAS programming within clinical trial environment.
  • Strong knowledge and practical experience with CDISC standards, including SDTM and ADaM.
  • Experience developing, reviewing, and validating clinical trial datasets and Tables, Listings, and Figures (TLFs).
  • Experience supporting clinical studies from study start-up through database lock, reporting, and regulatory submission.
  • Knowledge of regulatory submission requirements and experience supporting submissions to health authorities such as FDA, EMA, or PMDA.
  • Experience with clinical trial programming documentation, validation processes, and quality control practices.
  • CRO/vendor oversight experience preferred.
  • Demonstrated ability to manage multiple priorities while maintaining strong attention to detail and quality.
  • Excellent verbal, written, and interpersonal skills, with the ability to communicate effectively and collaborate with cross-functional teams in a remote/global environment.
  • Experience with Pinnacle 21 or similar CDISC validation tools preferred.
  • Experience with SAS macros, automation, and programming efficiency initiatives preferred.
  • Experience with R, Python, or other programming technologies preferred.

About Us:
Celcuity is a commercial biotechnology company pursuing development of targeted therapies for treatment of multiple solid tumor indications. The company's first FDA-approved product is REVTORPYK (gedatolisib), a potent, pan-PI3K and mTORC1/2 inhibitor that comprehensively blockades the PAM pathway. REVTORPYK is approved to treat adults with HR+/HER2- advanced breast cancer that progressed on prior endocrine therapy in the metastatic setting.
The Phase 3 VIKTORIA-2 trial is evaluating gedatolisib in combination with palbociclib and either fulvestrant or letrozole for the first-line treatment of HR+/HER2- locally advanced or metastatic breast cancer. A Phase 1/2 clinical trial evaluating gedatolisib in combination with darolutamide in patients with metastatic castration resistant prostate cancer, is ongoing.
Celcuity is an Equal-Opportunity Employer.
Celcuity is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are competitive. For this role, the anticipated base pay range is $160,000 - $185,000 DOE. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate's geography, qualifications, skills, and experience.
The successful candidate will be eligible for an annual performance incentive bonus and a new hire equity package. Celcuity also offers various benefits offerings, including, but not limited to, medical, dental, vision insurance, 401(k) match, PTO, and paid holidays.
Notice to Recruiters/Staffing Agencies
Recruiters and staffing agencies should not contact Celcuity through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees directly.
We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file. Celcuity's receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Celcuity and such organization and will be considered unsolicited. Celcuity will not be responsible for related fees.