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Clinical Data Management Programmer - SAS Programming

Pharmaceutical Product Development (PPD)

US-NC-Wilmingto

Submission for the position: Clinical Data Management Programmer - SAS Programming - (Job Number: 187595)Homebased U.S Full-Time Regular w/ Benefits Database position working with clinical trials data systems under general supervision. Provides technical leadership for some or all of the following activities: Designs and implements global library and study specific setup for clinical trials applications; develops and validates data checks; provides first-line end-user support/problem solving; provides support for application validation activities. Essential functions: Performs tasks following within the timelines established by the team, in accordance with the process outlined in the departmental procedures and indicated by the project contract. Designs, builds and tests project databases & edit checks. Defines and imports data into the system. Defines, creates and tests listings for data review and performs programming activities in line with project requirements. Acts as the lead on studies of simple to moderity complexity with close supervision. Researches and leverages resources to resolve issues and manage moderately complex tasks through the development and application of new knowledge and/or professional skills in areas including programming and technology. Participates in process improvement initiatives to increase efficiencies.•Increases knowledge and skills to gain good understanding of the lead programmer roles and overall department processes. Ensures adherence to departmental working practice documents and SOPs, and contributes to the development informal training materials. SAS specific essesntial functions: Data extraction from various databases (ex. Rave).

Working DM listings including DMdata cleaning listings, third party vendor data reconciliations, study deviation listing, coding listings. Proficiency in basic SAS SQL and SAS macros. Should have experience leading studies(end to end)

Setting up data import agreements between the vendors and the CRO.

Importing third party data of various forms (csv, xls, xlsx, xpt, sas) and running quality checks. Homebased U.S Full-Time Regular w/ Benefits Database position working with clinical trials data systems under general supervision. Provides technical leadership for some or all of the following activities: Designs and implements global library and study specific setup for clinical trials applications; develops and validates data checks; provides first-line end-user support/problem solving; provides support for application validation activities. Essential functions: Performs tasks following within the timelines established by the team, in accordance with the process outlined in the departmental procedures and indicated by the project contract. Designs, builds and tests project databases & edit checks. Defines and imports data into the system. Defines, creates and tests listings for data review and performs programming activities in line with project requirements. Acts as the lead on studies of simple to moderity complexity with close supervision. Researches and leverages resources to resolve issues and manage moderately complex tasks through the development and application of new knowledge and/or professional skills in areas including programming and technology. Participates in process improvement initiatives to increase efficiencies.•Increases knowledge and skills to gain good understanding of the lead programmer roles and overall department processes. Ensures adherence to departmental working practice documents and SOPs, and contributes to the development informal training materials. SAS specific essesntial functions: Data extraction from various databases (ex. Rave).

Working DM listings including DMdata cleaning listings, third party vendor data reconciliations, study deviation listing, coding listings. Proficiency in basic SAS SQL and SAS macros. Should have experience leading studies(end to end)

Setting up data import agreements between the vendors and the CRO.

Importing third party data of various forms (csv, xls, xlsx, xpt, sas) and running quality checks.

Minimum Required Education and Experience:

Bachelor’s degree in computer science, statistics, biostatistics, mathematics, biology or other health related field or equivalent experience that provides the skills and knowledge necessary to perform the job.

Minimum of 2 years experience in a clinical trials environment or similar field. Minimum of 1 years experience with Oracle or similar applications in a programming or administration capacity.

Additional expereince required for higher levels(Sr CDM Programmer)

Required Knowledge, Skills and Abilities:

Good organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines.Good computer skills

Knowledge of relational database systems (RDBMS) and structure

Experience in Oracle and with Oracle tools or similar, with working knowledge of SQL and/or PLSQL

Strong attention to detail and problem solving skillsGood written and verbal communication skills

Demonstrated experience in identification and resolution of technical problems in a professional environment

Ability to maintain a high degree of confidentiality with clinical data and client’s proprietary data

Ability to attain, maintain and apply a working knowledge of GCPs and applicable SOPsDemonstrated positive attitude, enthusiasm toward work, and the ability to work well with others.

Working Environment:

PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

Able to communicate, receive, and understand information and ideaswith diverse groups of peoplein a comprehensible and reasonable manner.

Able to work upright and stationary for typical working hours.

Ability to use and learnstandard office equipment andtechnologywith proficiency.

Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

May require travel. 5-10% annual possible.

PPD Defining Principles:

- We have a strong will to win - We earn our customer’s trust - We are gamechangers - We do the right thing -We are one PPD

If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, then please submit your application – we’d love to hear from you.

Minimum Required Education and Experience:

Bachelor’s degree in computer science, statistics, biostatistics, mathematics, biology or other health related field or equivalent experience that provides the skills and knowledge necessary to perform the job.

Minimum of 2 years experience in a clinical trials environment or similar field. Minimum of 1 years experience with Oracle or similar applications in a programming or administration capacity.

Additional expereince required for higher levels(Sr CDM Programmer)

Required Knowledge, Skills and Abilities:

Good organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines.Good computer skills

Knowledge of relational database systems (RDBMS) and structure

Experience in Oracle and with Oracle tools or similar, with working knowledge of SQL and/or PLSQL

Strong attention to detail and problem solving skillsGood written and verbal communication skills

Demonstrated experience in identification and resolution of technical problems in a professional environment

Ability to maintain a high degree of confidentiality with clinical data and client’s proprietary data

Ability to attain, maintain and apply a working knowledge of GCPs and applicable SOPsDemonstrated positive attitude, enthusiasm toward work, and the ability to work well with others.

Working Environment:

PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

Able to communicate, receive, and understand information and ideaswith diverse groups of peoplein a comprehensible and reasonable manner.

Able to work upright and stationary for typical working hours.

Ability to use and learnstandard office equipment andtechnologywith proficiency.

Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

May require travel. 5-10% annual possible.

PPD Defining Principles:

- We have a strong will to win - We earn our customer’s trust - We are gamechangers - We do the right thing -We are one PPD

If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, then please submit your application – we’d love to hear from you.

Submission for the position: Clinical Data Management Programmer - SAS Programming - (Job Number: 187595)

Job posted: 2021-04-16

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