Job Summary
Responsible for providing statistical programming support for the Biostatistics and Data Management functions for all clinical trials and regulatory submissions. Works closely with Biostatisticians and Data Managers to support creating SAS programs for independently validating selected tables, listings, and figures produced by programming vendors, for ad-hoc analyses, and to assist with data cleaning and query generation. Independently produces selected SDTM/ADaM files for analysis preparation and for validation of CRO CDISC work. Serves as a contact for programming activities being performed at assigned CROs.
Essential Duties and Responsibilities
- Provides SAS programming support to all clinical studies.
- Manages assigned programming CROs providing oversight and appropriate QC for programming deliverables.
- Provide statistical programming support for regulatory submissions (e.g., FDA, EMA), including electronic submission standards (eCTD).
- Provides primary programming and QC support for any internally produced outputs.
- Reviews and approves SAS programming instructions and CDISC/ADaM specifications.
- Performs statistical analysis and simulations using SAS to support clinical trial design and data interpretation.
- Reviews and provides input on eCRF design, external vendor data specifications, edit checks, and other Data Management related documents to ensure appropriate data collection for statistical programming.
- Works closely with biostatisticians and data managers to identify data issues and generate queries that may impact statistical analysis and/or programming.
- Works closely with biostatisticians and other functions (Pharmacovigilance, Clinical Development, etc.) to support data review for internal stakeholders.
- Assists with ensuring consistency across programming methods in similar studies within a program.
- Provides project management support, as needed, to ensure quality and timely completion of study milestones .
- Creates programming related SOPs, as necessary .
- Contributes to the management and administration of the Biometrics SAS server .
- Contributes to establishing and maintaining internal SAS programming conventions.
JOB QUALIFICATIONS
Education, Certifications, Experience
- Bachelor’s Degree equivalent with a minimum of 6 years of experience in SAS programming with at least 5 of those in a clinical research setting, or Master’s Degree with a minimum of 4 years of experience in SAS programming with at least 2 of those in a clinical research setting. Prefer industry experience in all phases of clinical research
Knowledge, Skills and Abilities
- Knowledge of pharmaceutical and regulatory requirements, procedures, and policies with a minimum of 5 years of pharmaceutical experience required.
- Experience with BLA or NDA/sNDA submissions is required.
- Knowledge of GCP, ICH, 21 CFR part 11, and other Guidance documents and policies related to clinical trials operations requirements.
- In depth knowledge of CDISC and ADaM dataset structures and requirements
- Proficiency with SAS programming skills to including knowledge of SAS ODS graphical procedures such as PROC SGPLOT and the graphics template language (GTL) Knowledge of all aspects of clinical drug development (Phase 1-4)
- Experience working with and managing a CRO partner.
- Excellent computer skills; strong verbal and written communication skills
- Ability to work well in a team environment as a contributor.
- Open, engaging, and transparent work style
- Ability to competently manage multiple competing priorities, switching priorities quickly as needs change. Must be comfortable working in a very fast-paced environment.
SPECIAL WORKING CONDITIONS
Office environment / Domestic - travel up to 10% may be necessary.Gossamer Bio is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants and complies with all applicable national, state and local laws governing nondiscrimination in employment.For California based applicants, the expected salary range for this position is $145,000 to $155,000. Actual pay will be determined based on experience, qualifications, and other job-related factors permitted by law.
Gossamer Bio is a multi-state employer, and this salary range may not reflect positions that work in other states.
ADD IF REMOTE /REMOVE IF SD ONLY:
This position is preferably located in San Diego, CA, however, we welcome candidates from all US territories as working remotely is a possibility. This position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. This position also qualifies for the benefits as listed below:
Gossamer Bio offers highly competitive benefit plans and programs, including medical, dental and vision insurance, 401(k) and 401(k) matching , long-term incentive plan, disability plan, vacation pay, sick time, holiday pay, and work, personal and family time off in accordance with the terms of the applicable plans. For additional general information on Company benefits, please visit
https://www.gossamerbio.com/work-at-gossamerbio/
The expected salary range for this position is listed below. Actual pay will be determined based on experience, qualifications, and other job-related factors permitted by law. This position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. This position also qualifies for the benefits as listed below.Gossamer Bio offers highly competitive benefit plans and programs, including medical, dental and vision insurance, 401(k) and 401(k) matching , long-term incentive plan, disability plan, vacation pay, sick time, holiday pay, and work, personal and family time off in accordance with the terms of the applicable plans.
For additional general information on Company benefits, please visit
https://www.gossamerbio.com/work-at-gossamerbio/
Pay Range$145,000—$155,000 USD
Vaccination Policy:
Gossamer Bio is committed to complying with federal, state and local law on vaccinations. Job candidates and employees should be aware that some roles may require full vaccination against COVID-19 . Gossamer Bio is an equal opportunity employer, and will provide reasonable accommodation to those unable to be vaccinated where it is not an undue hardship to the company to do so as provided under federal, state, and local law.
California Consumer Privacy Act (CCPA) Notice for California Residents:
This notice is to notify you that personal data about you has been collected by Gossamer Bio (“Controller”), which is located at 3115 Merryfield Row, Suite 120, San Diego CA 92121 and can be contacted by emailing privacy@gossamerbio.com, because Controller wishes to evaluate your candidacy for employment at Controller.Your personal data was either obtained from publicly available sources (e.g. LinkedIn) or provided to Controller by someone who referred you for potential employment. Controller’s Privacy team can be contacted at privacy@gossamerbio.com.
Your personal data will be processed for the purposes of managing Controller’s recruitment related activities, which include setting up and conducting interviews and tests for applicants, evaluating and assessing the results thereto, and as is otherwise needed in the recruitment and hiring processes. Such processing is legally permissible under Art. 6(1)(f) of Regulation (EU) 2016/679 (General Data Protection Regulation) and the California Consumer Privacy Act (CCPA) as necessary for the purposes of the legitimate interests pursued by the Controller, which are the solicitation, evaluation, and selection of applicants for employment.Your personal data has been shared with Greenhouse Software, Inc., a cloud services provider located in the United States of America and engaged by Controller to help manage its recruitment and hiring process on Controller’s behalf.
Your personal data will be retained by Controller as long as Controller determines it is necessary to evaluate your application for employment. Under the GDPR and CCPA, you have the right to request access to your personal data, to request that your personal data be rectified or erased, and to request that processing of your personal data be restricted. You also have to right to data portability. In addition, you may lodge a complaint with a supervisory authority.
