Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials.

Job Summary

Provide statistical programming support to clinical trials. Produce statistical analyses, including generating/validating analysis datasets, tables, listings, and figures for clinical trials. Create SDTM mapping and datasets. Develop and maintain the infrastructure for project files of SAS datasets and SAS code. Support Data Management in data set creations/transfers, integrity checks, and quality audits. Act as a liaison between clinical and subcommittees and project teams on an as-needed basis.

Primary Responsibilities

• Perform or oversee team in performing all statistical programming required for clinical trial analysis and reporting on large scale projects of high complexity

• Apply appropriate statistical methods for data analysis and provide statistical programming expertise for project teams

• Review the Statistical Analysis Plan in preparation for programming the planned analyses

• Lead design/development of SAS macros and other utilities to expedite SAS programming activities

• Organize and conduct internal training sessions and author papers for conferences

• Generate tables, listings, and figures per protocol, Statistical Analysis Plan, and/or approved client request

• Participate in statistical program validation and quality control activities

• Develop or review SDTM aCRF and specifications, ADaM specifications; complete programming and validation of CDISC SDTM and ADaM datasets

• Review pinnacle 21 reports and ensure compliance with CDISC and FDA guidelines

• Develop define.xml, study data reviewers guide and analysis datasets reviewers guide

• Identify study priorities and communicate effectively with project team and management

• Ensure quality, proper documentation and meet or exceed timely completion of the project within budgeted hours

• Manage statistical programming timelines, budgets, and client expectations

• Actively participate in study team meetings

• Interact with other departments, such as Clinical Operations, Project Management, and Data Management to ensure a high level of client satisfaction through successful execution of projects

• Participate in review process of study documents such as the CRF, edit check specifications, and database design specifications written by Data Management

• Program data cleaning checks, as necessary, to assist Data Management’s data cleaning activities

• Participate in installation/validation of statistical software packages throughout the software development lifecycle

• Develop and maintain the infrastructure for project files of SAS datasets and SAS code

• Mentor junior level statistical programmers by developing training plans and providing oversight of their work Ensure all programming activities and processes performed are conducted according to SDC’s standard procedures and/or sponsor requirements

• Adhere to all aspects of the SDC’s quality system

• Comply with SDC’s data integrity & business ethics requirements

• Perform other related duties incidental to the work described herein

• Adherence to all essential systems and processes that are required at SDC to maintain compliance to business and regulatory requirements

The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.

Required Skills

• Strong analytical skills, with the ability to process scientific and medical data.

• Very strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat, SAS Macros and SAS/Graph

• Strong problem-solving skills

• Able to work independently

• Excellent knowledge of statistical programming

• Proficient in manipulating and analyzing SAS data

• Ability to identify data issues, present problems, and implement solutions quickly

• Capability of communicating technical concepts clearly, concisely, and understandably to non-statistical colleagues

• Good organizational and time management skills, with the ability to multi-task

• Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP). Expert knowledge of CDISC SDTM and ADaM data models

• Very strong interpersonal communication, presentation, and leadership skills

• SAS Base, Advance and Clinical Trials Certification is preferred

Education or Equivalent Experience

Bachelor’s degree in computer science, statistics or other related, scientific field and at least eight years of relevant professional experience; or an equivalent combination of relevant education and/or experience.

Why SDC

SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances and positive work/life balance, we are able to attract some of the most talented people in the industry.

• We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits.

• We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment.

• We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.

• We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry.

• With a proven track record, SDC has been successfully executing client clinical programs since 2005.

Take a look at how you can join our team!

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Manager, Clinical Data Management

Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials.

Job Summary

Oversees and manages all aspects of Data Management Operations including staffing and resourcing, project management, operations management and client management. Applies a high level of technical expertise to effectively lead all Data Management tasks.

Primary Responsibilities

•         Oversees day-to-day data management operations, ensuring on-time and quality deliverables and excellent client service and satisfaction

•         Manages one or more key accounts and studies; interfaces with the client to address feedback, ensure risks and issues are resolved 

•         Serves as subject matter expert during client and vendor meetings

•         Leads teams located globally (Hyderabad locations) to deliver all aspects in Data Management including the Database build processes

•         Performs independent review or quality review of all team deliverables prior to sending to client

•         Performs all client communications across the DM functions; face to face, teleconferences and emails for lead role tasks.

•         Performs internal escalations, project status updates and project management functions including updates to PM systems

•         Actively supports business development in capabilities presentations to prospective and current clients

•         Effectively provides input for department and clinical study budgets

•         Liaises with internal and external cross-functional teams, sponsors, vendors, etc.

•         Serves as Project Manager on clinical studies, as needed

•         Works closely with Director of Data Management, Clinical Data Managers and Clinical Data Analyst to mentor data management staff

•         Ensures project work is planned, resource allocated and is successfully executed

•         Provides direction to staff when issues arise that the staff cannot resolve on their own

•         Ensures proper training and development of staff

•         Conducts regular meetings, actively manages performance and completes year-end performance reviews with all direct reports

•         Monitors performance of team and initiates process and resource improvement in partnership with Director of Data Management

•         Adheres to all aspects of the company’s quality system

•         Complies with the company’s data integrity and business ethics requirements

•         Performs other related duties incidental to the work described herein

•         Adherence to all essential systems and processes that are required at SDC to maintain compliance to business and regulatory requirements

The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.

Required Skills

•         Articulate and professional

•         Extensive experience in clinical research and Data Management in multiple therapeutic areas

•         Electronic Data Capturing (EDC) RAVE experience

•         Expert knowledge and understanding of ICH Guidelines for Good Clinical Practice and Title 21 of the Code of Federal Regulations

•         Strong project management abilities including analytical evaluation, organization, delegation, flexible team

•         management, negotiating and resource management skills

•         Effective leadership, budget forecast and implementation skills

•         May Require Travel up to 20%

Education or Equivalent Experience

·         Master’s degree (preferably in Engineering, Applied or Life Science) and at least three (3) years of experience in Clinical Data Management including leading several clinical studies, or a Bachelor’s degree (preferably in Engineering, Applied or Life Science) with a minimum of five (5) years in DM

·         One  year of experience direct management of personnel

·         Clinical research in a CRO setting is preferred.

Why SDC

SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances, positive work/life balance and 401k matching (US), we are able to attract some of the most talented people in the industry.

•             We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits.

•             We are passionate about our company culture. Our recognition program is  directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment. 

•             We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.

•             We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry.

•             With a proven track record, SDC has been successfully executing client clinical programs since 2005.

Take a look at how you can join our team!

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Principal Clinical Programmer (RAVE EDC)

Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials.

Job Summary

Lead in the evaluation, implementation, and validation of packaged systems. Create, maintain, and oversee processes for providing end user support in EDC systems. Build studies and support other users to build studies in EDC and other GxP systems. Works as part of a project team to design and implement clinical database applications in support of clinical research and biostatistics analysis. Processes database programming change requests. Documents all work fully according to FDA regulations and guidances, and company SOPs. Actively promotes standards for the development and acquisition of, and serve as the SME for, GxP systems. Mentors/trains junior level clinical programmers.

Primary Responsibilities

·       Lead the development, validation, and maintenance of clinical databases for clinical trials using a variety of validated software applications

·       Provide complete and accurate documentation of study databases consistent with company standard operating procedures (SOPs), study protocols and related data management plans

·       Develop and maintain global library of clinical database forms, edit checks, and other regularly used programs and routines

·       Implement and test data quality checks in accordance with the study data validation manual

·       Manage and develop programs for the reconciliation of external data from vendors (e.g., central lab data)

·       Serves as SME and facilitates integration of EDC systems to other clinical platforms such as CTMS, Reporting, IRT as needed

·       Assist in managing and updating medical coding dictionaries, including but not limited to MedDRA and WHODrug

·       Oversee the management of EDC, other GxP system user accounts and other help desk activities

·       Track issues in EDC systems, work with EDC vendors to resolve, and escalate issues appropriately to senior management.

·       Quickly learn new and/or advancements in software to become the SME for any technical question

·       Demonstrate good problem-solving skills, a proactive approach, and a willingness to make decisions, seeking advice when necessary

·       Facilitate and/or participate in writing departmental documentation (e.g., training documents, process guidance)

·       Exhibit good time management and organization skills; the ability to work in an efficient manner and prioritize tasks to meet tight deadlines while maintaining the highest standards of work

·       Keep management team abreast of issues, progress, and risks related to trial operations

·       Support bid defenses from a technical SME perspective

·       Participate in other clinical programming and data management activities, as required

·       Participate in internal and external team meetings, as required

·       Mentor junior level clinical programmers

·       Adhere to all aspects of the Statistics & Data Corporation’s quality system

·       Comply with Statistics & Data Corporation’s data integrity & business ethics requirements

·       Perform other related duties incidental to the work described herein

The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.

Required Skills

·       At least eight years’ experience assuming lead database programming responsibilities on projects, with a minimum of 5 years in a clinical environment

·       Excellent understanding of relational database structures

·       Fast, accurate programming skills using assorted application software

·       PL/SQL, SQL, and XML programming skills

·       Solid interpersonal skills, with the ability to work well with people of all levels of expertise and comfort in varied organizational relationships

·       Demonstrated ability to provide both “user-friendly” and technical documentation

·       Ability to provide expertise to guide department in continued efficiency and growth

·       Knowledge and experience with FDA regulations and guidances (e.g., 21 CFR Part 11, ICH/GCP)

·       Knowledge of installation and/or validation of clinical data management system (CDMS) applications in a clinical research environment

·       C#, C++, .NET, Visual Basic or other object-oriented language, and/or SAS programming knowledge / experience not required, but desirable

·       Medidata Rave and iMedNet EDC knowledge / experience not required, but desirable

Reporting application development (e.g., JReview, Business Objects, PowerBI) knowledge / experience not required, but desirable

Education or Equivalent Experience

·       Bachelor’s degree in computer science or other quantitative or scientific discipline with 8+ years’ experience in database programming and demonstrated working knowledge of scientific principles.

·       Commensurate experience with clinical database programming and database administration will be considered as an alternative to a degree

Why SDC

SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances and positive work/life balance, we are able to attract some of the most talented people in the industry.

• We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits.

• We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment.

• We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.

• We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry.

• With a proven track record, SDC has been successfully executing client clinical programs since 2005.

Take a look at how you can join our team!

#LI-Hybrid

See more jobs at Statistics & Current Openings

Apply for this job

Interactive Response Technologies - Project Manager

Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005.

SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials.

Job Summary

Oversees and coordinates all lRT activities in support of clinical and/or non-clinical research studies for study initiation, setup, maintenance, and closeout. Manages the day-to-day IRT project activities including, but not limited to, timelines, budgets, staff, project scope, reports and communication for the lifecycle of the project(s). Mentors/trains IRT Programmer on IRT build requirements

Primary Responsibilities

·        Lead IRT study setup activities including IRT design and specification (with edit checks) documents and approval and user acceptance testing.

·        Allocate and prioritize workloads for multiple projects

·        Serve as primary client contact for IRT

·        Work with Clinical Data Managers and Statistical Leads with management of timelines and budgets as they pertain to IRT activities

·        Work with study team to reconcile IRT data with clinical data and oversees data transfers

·        Mentor IRT Programmer on IRT build requirements

·        Develop documentation for validation and maintenance of IRT databases for clinical trials using a variety of validated software applications

·        Maintains quality control of the data, project deliverables and closeouts

·        Adhere to all aspects of the SDC's quality system

·        Comply with SDC's data integrity & business ethics requirements

·        Develop and maintain SOPs and tools relating to the IRT

·        Perform other related duties incidental to the work described herein

·        Adherence to all essential systems and processes that are required at SOC to maintain compliance to business and regulatory requirements 

The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.

Required Skills

·        Exceptional working knowledge of clinical trials and IRT role in the clinical trials process

·        A minimum of 1 year of staff mentoring and leadership experience

·        Strong leadership capabilities

·        Strong delegation abilities

·        Highly effective communication skills, both written and verbal

·        Ability to work as a member of a multi-disciplinary team and adapt to changing priorities

·        Training and experience in clinical database management

·        General knowledge of GCPs and the conduct of clinical trials.

·        Understanding of the clinical research process flow and drug development processes.

·        Understanding of software development and testing processes.

·        Demonstrated proficiency in office productivity applications (e.g., Microsoft Word, PowerPoint, and Excel).

·        Excellent organizational skills

·        Ability to manage multiple tasks simultaneously and to prioritize tasks effectively.

·        Demonstrated ability to focus on project work and efficiently bring projects to completion

·        Ability to effectively manage projects, budgets and timelines

·       Ability to learn new systems without formal training

Education or Equivalent Experience

Bachelor's degree in engineering, applied or life science and at least two (2) years of experience in management of an IRT system or an Associate's degree in engineering, applied or life science and a minimum of five (5) years of experience in management of an IRT system.

Why SDC

SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances and positive work/life balance, we are able to attract some of the most talented people in the industry.

• We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits.

• We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment.

• We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.

• We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry.

• With a proven track record, SDC has been successfully executing client clinical programs since 2005.

Take a look at how you can join our team!

#LI-Hybrid

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Manager, Data Insights & Automation

SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances and positive work/life balance, we are able to attract some of the most talented people in the industry.

Job Summary

Lead and manage the effort to clean, process, store and analyze clinical data with its application towards research and development of Artificial Intelligence (AI) and Machine Learning (ML) algorithms supporting better understanding of the safety and efficacy of new therapies. Contribute to the organization’s strong drive to be at forefront of using AI in clinical trials to simplify data processing and discover imperceptible correlations. 

Lead and manage software development activities to drive automation across SDC departments reducing error and increasing efficiency across those departments.  Serve as the primary point within the company driving standardization.

Primary Responsibilities

·        Oversees day to data activities involving custom software, data engineering and automation.

·        Develop standard metrics demonstrating model performance, robustness, and validity.

·        Engage with various internal departments such as data management, technology solutions, biostatistics, IT, and business development to strategically identify areas to develop automations, apply AI and/or ML toward increasing the efficiency of processes and detecting information trends.

·        Ensure that algorithms can be practically deployed with minimal resource usage and maximum ease of use in existing architecture.

·        Deliver high quality software design documentation

·        Prototype new ideas/technologies to create proof of concept and demos

·        Contribute to the development of standard operating procedures for the use of artificial intelligence within clinical trials.

·        Perform other related duties incidental to the work described herein.

·        Adherence to all essential systems and processes that are required at SDC to maintain compliance to business and regulatory requirements

The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.

Required Skills

·        Fluency in Python with experience parsing, manipulating, and converting data to and from a wide range of formats (CSV, json, XML, html, SQL tables, etc.)

·        Experience in designing and deploying production applications.

·        System design capabilities to improve operational efficiency and costs.

·        Experience in the software development lifecycle.

·        Experience mentoring and managing other team members.

·        Experience in writing and implementing policy and procedures.

·        Ability to work with stakeholders to translate business requirements into clear technical specifications.

·        Ability to communicate effectively in writing and verbally.

·        Ability to identify issues, present problems, and implement solutions.

·        Capability of communicating technical concepts clearly, concisely, and understandably to non-technical colleagues

·        Good leadership, organizational and time management skills, with the ability to multi-task

Strong interpersonal communication and presentation skills

Education or Equivalent Experience

A Master’s degree in statistics, engineering, operations research, mathematics, computer science, business analytics or other related field, with focus in artificial intelligence preferred, and at least 5+ years of relevant professional experience or a bachelor’s degree with 7+ years of relevant professional experience

Why SDC

• We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits.

• We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment.

• We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.

• We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry.

• With a proven track record, SDC has been successfully executing client clinical programs since 2005.

Take a look at how you can join our team!

#LI-Hybrid​

See more jobs at Statistics & Current Openings

Apply for this job

Software Developer (Python & Backend)

SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances and positive work/life balance, we are able to attract some of the most talented people in the industry.

Job Summary:

The Software Developer will develop and maintain business process automation(s) to automate steps within the CRO operations lifecycle. This includes acting on local flat files, integrating with APIs as well as operating with databases. The role contributes to the organization’s strong drive to be at the forefront of using Artificial Intelligence (AI) in clinical trials to simplify data processing and discover imperceptible correlations.

Primary Responsibilities

• Develops and maintains existing automation applications using test driven development

• Assists in the design of new applications

• Maintain Azure based cloud-based resources

• Engages with various internal cross-functional departments to develop and implement software applications while understanding the underlying data

• Delivers high quality software test and code documentation

• Contributes to the development of standard operating procedures for the use of artificial intelligence and software development within clinical trials

• Prototypes new ideas/technologies to create proof of concept and demos

• Provides mentorship for associate software developers

• Adherence to all essential systems and processes that are required at SDC to maintain compliance to business and regulatory requirements

• Act as a resource for other team members for debugging, code reviews and other software development lifecycle activities

The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.

Required Skills

• Fluent in Java Script and Proficient in Python.

• Experience with REST APIs

• Experience in the software development lifecycle.

• Ability to work with stakeholders to translate business requirements into clear technical specifications

• Ability to communicate effectively in writing and verbally.

• Ability to identify issues, present problems, and implement solutions

• Capability of communicating technical concepts clearly, concisely, and understandably to non-technical colleagues

• Good organizational and time management skills, with the ability to push forward multiple projects simultaneously

• Strong interpersonal communication and presentation skills

Education or Equivalent Experience

• Bachelor’s degree in a technical field with 4 years of technical experience with the last 2 years being a Software Development centric role

OR

• 6+ years in a technical role with the last 2 years being a Software Development centric role

Why SDC

We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits.

We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment.

We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.

We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry.

With a proven track record, SDC has been successfully executing client clinical programs since 2005.

Take a look at how you can join our team!

See more jobs at Statistics & Current Openings

Apply for this job