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PSI CROPC

SAS Developer (SDTM)

PSI CRO is a global, full-service Contract Research Organization (CRO) founded in 1995, specializing in predictable patient enrollment and on-time delivery of clinical trials across various therapeutic areas. Headquartered in Switzerland, PSI operates in over 50 countries with a strong focus on quality and client satisfaction.

PSI CRO

Employee count: 1001-5000

Mexico only

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We are currently looking for a knowledgeable and proactive SAS Developer to join our global Data Management team.
Please note the official PSI CRO job title will be: Database Developer.

If you are keen to provide the full range of clinical database development and programming services, ensure high quality, accuracy, and consistency of clinical data, and be involved in something new, outstanding and challenging, this job opportunity is perfect for you!

Responsibilities:

  • Communication point for data management and statistics on matters of database programming and deliverable database development
  • Clinical database (EDC) requirements/structure review and testing
  • Data validation plan review and programming of data validation procedures
  • Generation of clinical database listings and reports to support clinical trial data collection, tracking, review and validation
  • Programming of patient profiles
  • Participate and support the development of Study Data Tabulation Model (SDTM) (define.xml, annotated CRF, reviewer’s guide) and programming of data transformation from raw data sources into CDISC-complaint deliverable
  • Validation of clinical trial data according to SDTM specifications
  • Deliverable database transfer to clients; electronic data transfers
  • Liaison with vendors and clients regarding electronic data transfer specifications
  • Receipt and validation of electronic data transfers
  • College or University degree (IT, programming, technical education)
  • Full working proficiency in English
  • At least two years of industry experience
  • Knowledge of and experience in the SAS programming language (Base SAS, SAS/Macros, SAS/ODS) is required
  • Knowledge of and experience in SQL
  • Experience in Clinical Data Management systems (like Medidata/Veeva) is desirable
  • Knowledge of CDISC standards is a plus
  • Proficient user of standard MS Office applications and MS Access
  • Experience in a professional environment, preferably with clinical or medical data

Only CVs in English will be considered.

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then this is the right choice for you.

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

About the job

Apply before

Posted on

Job type

Full Time

Experience level

Mid-level

Education

Bachelor degree

Experience

2 years minimum

Location requirements

Hiring timezones

Mexico +/- 0 hours

About PSI CRO

Learn more about PSI CRO and their company culture.

View company profile

We are a leading full-service global Contract Research Organization (CRO) with a key strength in predictable patient enrollment across multiple therapeutic areas. Since our founding in 1995 by Dr. Robert Reekie and Dr. Roger A. Smith, we've been dedicated to revolutionizing how clinical trials are conducted, focusing on delivering high-quality, cost-effective solutions worldwide. Our mission is to be the best CRO in the world as measured by our employees, clients, investigative sites, and vendors. This commitment is reflected in our exceptionally high repeat and referral business rates and minimal staff turnover.

Our global reach allows us to conduct clinical trials across multiple continents and in over 50 countries. We are known in the industry for our 'on-time project delivery,' a reputation we've built by investing substantial effort and medical expertise into performing quality feasibility assessments that provide accurate predictors of study timelines. In fact, over 90% of our studies finish on time or ahead of schedule. We specialize in planning and executing global pivotal registration clinical trials, particularly in complex areas like oncology, hematology, infectious diseases, gastroenterology, multiple sclerosis, and rare indications. We embrace innovation and technology, leveraging cutting-edge methodologies and data-driven insights to optimize trial design, streamline operations, and enhance patient engagement. Our robust quality management systems and adherence to the highest industry standards, including ISO 9001:2015 and ISO 27001:2013 certifications, underscore our dedication to excellence. We are proud of our contributions to advancing healthcare by helping bring life-saving therapies and treatments to market. We actively engage in research collaborations and knowledge sharing to contribute to scientific advancement.

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PSI CRO

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