Clinical Programmer II

Otsuka Pharmaceutical Co., Ltd; Palo Alto (CA); On-site; USD 145,604 - 156,347; Full time

Job summary

Otsuka Pharmaceutical Co., Ltd is looking for a Senior Clinical Programmer to support clinical trials by designing and maintaining clinical data management systems. This role is hybrid in Palo Alto, California and requires expertise in R and a solid understanding of clinical trial processes.

Candidates should have at least 5 years of experience or equivalent qualifications. They will work closely with cross-functional teams and provide guidance on data processing. Salary ranges from $145,604 to $156,347 annually.

Qualifications

• Minimum of 5 years of related experience; a Master's degree with 3 years of experience may substitute.
• Comprehensive understanding of clinical trial processes and data flow.
• Excellent communication and interpersonal skills.

Responsibilities

• Design and develop custom applications and tools for data collection.
• Collaborate with teams including clinical operations and biostatistics.
• Generate reports and visualizations for clinical studies.

Skills

R programming

Python

SQL

SAS

Data visualization tools

Version control (Git)

Education

Bachelor's degree in computer science, statistics, life sciences, or a related field

Master's degree with relevant experience

Tools

Power BI

Tableau

Job description

## Senior Clinical ProgrammerApplyremote type: Hybridlocations: Palo Altotime type: Full timeposted on: Posted 5 Days Agojob requisition id: R12036At Recor Medical, we are pioneering Ultrasound Renal Denervation (uRDN) therapy to treat hypertension, the leading cardiovascular risk factor in the world. With our ParadiseTM uRDN System, we’re on a mission to provide the millions of people who suffer from hypertension with a non-drug and minimally invasive option to lower their blood pressure. Join us on our journey and make a meaningful impact on the lives of people around the globe.**Position Summary**The Senior Clinical Programmer at ReCor Medical requires complete knowledge and full understanding of clinical programming principles and practices for medical device clinical trials. Responsible for designing, developing, and maintaining clinical data management systems that support regulatory submissions and ensure data integrity throughout clinical trials. Works independently to solve diverse problems related to clinical data processing, applying sophisticated analytical techniques to identify and resolve complex issues. Collaborates with cross-functional teams while providing technical guidance on clinical data processing methodologies.**Responsibilities and Duties*** Design and develop custom applications, scripts, and tools for clinical data collection, processing, and analysis* Establish and enforce data standardization practices (e.g., CDISC, SDTM, ADaM)* Collaborate with cross-functional teams including clinical operations, biostatistics, and regulatory affairs* Assess unusual circumstances and use sophisticated analytical techniques to identify and resolve complex data issues* Generate reports and visualizations for clinical studies* Program, validate, and maintain table listings and figures (TLFs) for clinical study reports and regulatory submissions* Create and maintain data integration pipelines between clinical systems and internal databases* Provide technical guidance to junior programmers on clinical data processing methodologies* Other Duties as assigned.**Requirements*** Bachelor's degree in computer science, statistics, life sciences, or a related field with a minimum of 5 years of related experience; or Master's degree with 3 years of experience; or equivalent work experience.* Proficiency in R, with experience in other relevant programming languages (e.g., Python, SQL, SAS).* Comprehensive understanding of clinical trial processes, data flow, and clinical trial data standards (e.g., CDISC SDTM, ADaM).* Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and explain technical concepts to non-technical stakeholders.* Knowledge of regulatory requirements and experience preparing programming deliverables for submissions to regulatory agencies.**Preferred Skills*** Experience with data visualization tools (e.g., Power BI, Tableau)* Proficiency in version control systems (e.g., Git) and collaborative development practices* Experience mentoring junior programmers and conducting code reviews* Familiarity with cloud-based data platforms and integration technologies* Experience with software validation per FDA guidelines* Knowledge of machine learning or advanced analytics techniques applicable to clinical dataSalary range: $145,604- $156,347 (Annual Base Salary)The successful candidate's starting base pay will be determined based on job-related skills, experience, qualifications, work location and market conditions. The expected base pay range for this role may be modified based on market conditions.**Equal Employment Opportunity** At Recor Medical, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.**Pre-Employment Requirement**At Recor Medical, patient safety and compliance are at the heart of everything we do. To support these standards, employment for all field-based roles is contingent upon successfully completing a pre-employment background check and/or drug screen. These steps help ensure we bring the highest level of integrity and accountability to the physicians and patients we serve.**Radiation Safety Requirement**Certain field-based roles at Recor Medical require work in environments where radiation sources (e.g., x-ray equipment) are in use. Employees in these roles will be issued a personal dosimetry badge to monitor occupational exposure and are required to wear it in accordance with company policy and applicable regulatory standards. This program is designed to ensure compliance with federal and state regulations and to maintain radiation exposure at levels that are As Low As Reasonably Achievable (ALARA). Additional guidance and protective equipment, as necessary, will be provided as part of onboarding and ongoing safety training.Respecting your privacy is an essential part of the Company’s privacy program and we are committed to the proper handling of Personal Information collected or processed in connection with an Applicant’s application for employment, a Contract Worker’s work, or a Former Employee’s employment at Recor. Refer to our Applicant, Contract Worker & Former Employee Privacy Policy for more detail information.