Data Scientist Socar Research, located in Nyon, Switzerland, is a leading Functional Service Provider with over 30 years of experience in providing clinical research and technology services to the pharmaceutical, biotechnology and medical device industries. SOCAR is seeking an experienced Data Scientist.
Responsibilities:
Design and develop eCRFs and user guidance.
Configure the EDC system to trial requirements.
Perform and oversee user acceptance testing, training, and database release activities.
Program edit checks and data queries.
Program status and metric reports.
Develop Data Management documentation such as DM plan and database validation plan.
Develop and implement data transfer agreements with third parties.
Provide support to end users.
Review DM standard operating procedures.
Ensure study timelines are met and data quality meets high industry standards.
Lock, transfer, and archive databases.
Required profile:
Master’s degree in computer science, physics, mathematics, or equivalent experience.
At least two years of clinical database development experience.
Experience with Electronic Data Capture (EDC) systems.
Experience working with Oracle and clinical database applications.
Knowledge of SQL, PL/SQL, SAS, and CDISC is a plus.
Fluency in English (oral and written).
Understanding of the clinical research environment and global regulatory requirements such as ICH GCP and CFR 21 part 11.
Analytical mindset with problem‑solving skills.
Detail‑oriented with excellent organizational and communication skills.
Clinical Research Associate (CRA) Socar Research, located in Nyon, Switzerland, is a leading Functional Service Provider with over 30 years of experience in providing clinical research and technology services to the pharmaceutical, biotechnology and medical device industries. SOCAR is seeking an experienced Clinical Research Associate (CRA).
Responsibilities:
Perform remote site visits, write up visit reports, follow up and resolve issues from visits.
Perform source data/document verification (SDV) remotely and onsite.
Perform remote monitoring and site management activities.
Maintain the electronic Trial Master File (eTMF).
Perform data management activities such as tracking eCRF completion and data cleaning.
Limited travel to sites.
Profile:
Medical‑related scientific degree (Bachelor, Master, PhD, nursing qualifications or similar).
At least three years of experience as a Clinical Research Associate.
Strong knowledge of ICH‑GCP, Swiss and other international laws and regulations governing clinical trials.
Strong medical/clinical knowledge.
Excellent clinical trial monitoring skills with high attention to detail and sound problem‑solving skills.
Excellent interpersonal communication skills (verbal and written).
Ability to prioritise multiple tasks and meet project timelines.
Computer skills (MS Office) and experience with eCRF, CTMS, and eTMF software.
Fluent in English and German (written and spoken); French and Italian are a plus.
Commitment to consistently high‑quality work.
Statistician Socar Research, located in Nyon, Switzerland, is a leading Functional Service Provider with over 30 years of experience in providing clinical research and technology services to the pharmaceutical, biotechnology and medical device industries. SOCAR is seeking an experienced Statistician.
Responsibilities:
Participate in the development and writing of Statistical Analysis Plans (SAP).
Program analysis datasets, including data derivations and data mapping.
Provide statistical review/input on study protocols.
Perform statistical analyses per the SAP.
Develop programs and generate tables, listings, and figures for trial or project reports.
Participate in the writing of the statistical report.
Participate in programming edit checks and setting up the trial database using SQL code.
Perform sample size calculations.
Profile:
MSc in Statistics or Mathematics with at least three years of practical experience as a Statistician or SAS programmer.
Knowledge of statistics applied to clinical studies.
Knowledge of international standards (ICH, GCP, CDISC).
Proficiency in SAS base and macro; knowledge of SQL and PL/SQL is a plus.
Excellent interpersonal communication skills (verbal and written).
Understanding of clinical trial statistical concepts such as descriptive statistics, hypothesis testing, and time‑to‑first‑event analysis.
Understanding of CDISC data models, especially SDTM and ADaM.
Ability to analyze problems and formulate ideas in a structured logical manner.
Fluent in English (verbal and written).
Commitment to consistently high‑quality work.
If you possess a valid Swiss work permit and fit the profile required for these positions, please forward your application to info@socar.ch. We will only respond to candidates who fit the profile.
Socar is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, genetic information, or any other characteristic protected by law.
Only direct applications will be considered for these vacancies. We do not accept speculative CVs or candidate profiles.
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Responsibilities:
Design and develop eCRFs and user guidance.
Configure the EDC system to trial requirements.
Perform and oversee user acceptance testing, training, and database release activities.
Program edit checks and data queries.
Program status and metric reports.
Develop Data Management documentation such as DM plan and database validation plan.
Develop and implement data transfer agreements with third parties.
Provide support to end users.
Review DM standard operating procedures.
Ensure study timelines are met and data quality meets high industry standards.
Lock, transfer, and archive databases.
Required profile:
Master’s degree in computer science, physics, mathematics, or equivalent experience.
At least two years of clinical database development experience.
Experience with Electronic Data Capture (EDC) systems.
Experience working with Oracle and clinical database applications.
Knowledge of SQL, PL/SQL, SAS, and CDISC is a plus.
Fluency in English (oral and written).
Understanding of the clinical research environment and global regulatory requirements such as ICH GCP and CFR 21 part 11.
Analytical mindset with problem‑solving skills.
Detail‑oriented with excellent organizational and communication skills.
Clinical Research Associate (CRA) Socar Research, located in Nyon, Switzerland, is a leading Functional Service Provider with over 30 years of experience in providing clinical research and technology services to the pharmaceutical, biotechnology and medical device industries. SOCAR is seeking an experienced Clinical Research Associate (CRA).
Responsibilities:
Perform remote site visits, write up visit reports, follow up and resolve issues from visits.
Perform source data/document verification (SDV) remotely and onsite.
Perform remote monitoring and site management activities.
Maintain the electronic Trial Master File (eTMF).
Perform data management activities such as tracking eCRF completion and data cleaning.
Limited travel to sites.
Profile:
Medical‑related scientific degree (Bachelor, Master, PhD, nursing qualifications or similar).
At least three years of experience as a Clinical Research Associate.
Strong knowledge of ICH‑GCP, Swiss and other international laws and regulations governing clinical trials.
Strong medical/clinical knowledge.
Excellent clinical trial monitoring skills with high attention to detail and sound problem‑solving skills.
Excellent interpersonal communication skills (verbal and written).
Ability to prioritise multiple tasks and meet project timelines.
Computer skills (MS Office) and experience with eCRF, CTMS, and eTMF software.
Fluent in English and German (written and spoken); French and Italian are a plus.
Commitment to consistently high‑quality work.
Statistician Socar Research, located in Nyon, Switzerland, is a leading Functional Service Provider with over 30 years of experience in providing clinical research and technology services to the pharmaceutical, biotechnology and medical device industries. SOCAR is seeking an experienced Statistician.
Responsibilities:
Participate in the development and writing of Statistical Analysis Plans (SAP).
Program analysis datasets, including data derivations and data mapping.
Provide statistical review/input on study protocols.
Perform statistical analyses per the SAP.
Develop programs and generate tables, listings, and figures for trial or project reports.
Participate in the writing of the statistical report.
Participate in programming edit checks and setting up the trial database using SQL code.
Perform sample size calculations.
Profile:
MSc in Statistics or Mathematics with at least three years of practical experience as a Statistician or SAS programmer.
Knowledge of statistics applied to clinical studies.
Knowledge of international standards (ICH, GCP, CDISC).
Proficiency in SAS base and macro; knowledge of SQL and PL/SQL is a plus.
Excellent interpersonal communication skills (verbal and written).
Understanding of clinical trial statistical concepts such as descriptive statistics, hypothesis testing, and time‑to‑first‑event analysis.
Understanding of CDISC data models, especially SDTM and ADaM.
Ability to analyze problems and formulate ideas in a structured logical manner.
Fluent in English (verbal and written).
Commitment to consistently high‑quality work.
If you possess a valid Swiss work permit and fit the profile required for these positions, please forward your application to info@socar.ch. We will only respond to candidates who fit the profile.
Socar is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, genetic information, or any other characteristic protected by law.
Only direct applications will be considered for these vacancies. We do not accept speculative CVs or candidate profiles.
#J-18808-Ljbffr
