Career

Key responsibilities

  • Management of clinical trials through review, computerization, cleaning and auditing of clinical data and databases in compliance with standard operating procedures, client guidelines and regulatory agency guidelines;
  • Data Management Plan Development;
  • Development of Case Report Form electronic and/or paper;
  • Development database clinical trials data specifications, including eCRF, user requirements, edit rules/checks, query logic and data validations;
  • Assistance in Data Management process;
  • Participation in system testing and test case validating;
  • Generation of data retrievals and summaries;
  • Coordination of department activities;
  • Assistance in system testing;
  • Providing training to department staff;
  • Overseeing the process of archiving, storing, updating and retrieving of data management documents

Requirements

  • MD or University degree in Life Sciences;
  • Fluent English, written and spoken;
  • Excellent verbal and written skills;
  • Good organizational, interpersonal and team skills;
  • Demonstrated computer skills (MS Office Applications);
  • Experience in working with medical documents.

We offer:

  • Challenging job in a highly qualified team;
  • Employee-friendly work environment;
  • Competitive salary;
  • Professional growth in clinical research field.
Attach your CV

Key responsibilities

  • CRF development
  • Participating in creation and deploying data bases and apps for clinical trials
  • Coordinating data entering
  • Data verification and coding
  • Participating in department’s document workflow

Requirements

  • Graduate medical / pharmaceutical / biological education
  • Working with medical documentation
  • Experienced PC user English – Upper Intermediate

We offer:

  • Challenging job in a highly qualified team;
  • Employee-friendly work environment;
  • Competitive salary;
  • Professional growth in clinical research field.
Attach your CV

Key responsibilities

  • Manage the data management team, including resource planning, recruitment, performance evaluation and training;
  • Develop supporting staff skills, encourage growth and provide regular performance feedback;
  • Set clear goals and objectives;
  • Manage work priorities, delegating responsibilities where appropriate;
  • Monitor compliance;
  • Provide training/development to the team;
  • Ensure timelines and quality standards within the group are met;
  • Development, review and approval of departmental working instructions and SOPs;
  • Review of clinical documentation;
  • Develop department budget and resource forecasting;
  • Identify and implement solutions to project data management issues and concerns, including proactive prevention strategies based on metrics and forecasts;
  • Advanced planning and risk management for projects (issue escalation, resource management);
  • Identify areas for process and efficiency improvement and implement solutions on assigned projects;
  • Support achievement of project revenue and operating margin for data management activities to agreed targets;
  • Support business development for data management time and cost estimates and present to potential clients on global data management capabilities;
  • Participate in bid defense meetings and company presentations;
  • Assist company software developers when needed;

Requirements

  • 3+ years of relevant career experience in a Clinical Data Management environment;
  • At least 2 years of experience as a Line Manager/Data Management Lead or Project Manager;
  • MD or University degree in Life Sciences;
  • Ability to lead and manage group of data managers;
  • Excellent data management and technical required skills;
  • Ability to work effectively and successfully in a team environment;
  • Effective communicator with excellent organizational skills;
  • Ability to provide quality output and deliverables, in adherence with challenging timelines;
  • Fluent English;

We offer:

  • Challenging job in a highly qualified team;
  • Employee-friendly work environment;
  • Competitive salary;
  • Professional growth in clinical research field
Attach your CV

Key responsibilities

  • Management of clinical trials through review, computerization, cleaning and auditing of clinical data and databases in compliance with standard operating procedures, client guidelines and regulatory agency guidelines;
  • Data Management Plan Development;
  • Development of Case Report Form;
  • Review of clinical documentation;
  • Development, review and approval of department working instructions and SOPs;
  • Development database clinical trials data specifications, including eCRF, user requirements, edit rules/checks, query logic and data validations;
  • Assistance in Data Management process;
  • Participation in system testing and test case validating;
  • Generation of data retrievals and summaries;
  • Coordination of department activities;
  • Assistance in system testing;
  • Providing training to department staff;
  • Overseeing the process of archiving, storing, updating and retrieving of data management documents;
  • Support business development for data management time and cost estimates and present to potential clients on global data management capabilities.

Requirements

  • MD or University degree in Life Sciences;
  • at least 2 years of experience in data management;
  • Fluent English, written and spoken;
  • Excellent verbal and written skills;
  • Good organizational, interpersonal and team skills;
  • Demonstrated computer skills (MS Office Applications);
  • Experience in working with medical documents;

We offer:

  • Challenging job in a highly qualified team;
  • Employee-friendly work environment;
  • Competitive salary;
  • Professional growth in clinical research field.

 

Attach your CV

Key responsibilities

  • Data review and statistical analysis;
  • Development of statistical analysis plans (SAPs), table, figure and listing (TFL) shells, programming and table specifications;
  • Statistical analysis report development (SAR);
  • Assistance with protocol development, sample size calculation, protocol and case report form (CRF) review;
  • Writing detailed statistical analysis plans, including specifications for analysis files and TFLs;
  • Support, plan, review and analyze clinical studies;
  • In collaboration with medical writers co-authoring final integrated reports of clinical trial data by writing thorough and clear statistical methods sections and producing the statistical appendix for the final report;

Requirements

  • Master’s degree in Statistics, Biostatistics, Mathematics or related field;
  • Strong experience working with SAS;
  • Sound knowledge of statistical methodology and experience in international pharmaceutical development;
  • Fluent English, written and spoken;
  • Excellent verbal and written skills;
  • Good organizational, interpersonal and team skills;

We offer:

  • Challenging job in a highly qualified team;
  • Employee-friendly work environment;
  • Competitive salary;
  • Professional growth in clinical research field.
Attach your CV

Key responsibilities

  • Responsible for processing of clinical data required for analysis of clinical trials for Phase 1-4;
  • Develop SAS coding and table templates for preparing, processing and analyzing clinical data;
  • Generate and QC summary tables, data listings and graphs for in-house analyses of study data or publications using SAS standard coding practices;
  • Validate the programmed analysis datasets, tables, listing and figures;
  • Prepare clinical and statistical summary reports;
  • Create/review programming plan, specifications for datasets and TLFs;
  • Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues.

Requirements

  • A minimum of a Bachelor's degree in Computer Science, Mathematics, Statistics, Pharmaceuticals Sciences, Life Sciences and related areas is required. A Masters or PhD is preferred;
  • Familiar with CDISC standards, ICH/GCP, 21 CFR Part 11, ICHE9, ICHE6, ICHE3 guidelines;
  • Excellent knowledge of SAS programming and associated features and their applications in pharmaceuticals industry environment including clinical trial data setting;
  • Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results;
  • Thorough understanding of relational database components and theory;
  • Excellent oral and written communication skills;

We offer:

  • Challenging job in a highly qualified team;
  • Employee-friendly work environment;
  • Competitive salary;
  • Professional growth in clinical research field.
Attach your CV

Key responsibilities

  • Review of requirements;
  • Communication with the team of developers and analysts;
  • functional and load testing of the company's products;
  • Writing and maintaining of test documentation;
  • The use of automation of testing processes.

Requirements

  • Bachelor's degree in Computer Science, Mathematics
  • Knowledge of the theory of testing, life cycle software;
  •  Familiarity with modern development and testing methodologies;
  • 1+ year of testing experience
  • Working with test documentation
  • Working with Bug reporting
  • Preferable:

    • Skills and knowledge of test automation tools;

    • Knowledge and experience with the DBMS (MSSQL, PostgreSQL);

    • Experience with jira, confluence;

    • English (pre-Intermediate and higher);

    • API testing experience

    • Excellent oral and written communication skills.

We offer:

  • Challenging job in a highly qualified team;
  • Employee-friendly work environment;
  • Competitive salary;
  • Professional growth in clinical research field.
Attach your CV

Key responsibilities

  • Managing the development backend team (5 - 10 people);
  • Interaction with experts in understanding the best way to implement solutions;
  • assessment of product requirements in terms of labor costs;
  • Making decisions on how to implement the requirements, considering the pros and cons of the respective implementations;
  • Quality control of the final implementation, review of the code;
  • Participation in the development of project documentation;
  • Direct participation and process control;
  • Interaction with the testing team, DevOps, technical writers, support staff;
  • Direct involvement in code writing for complex, critical tasks;

Requirements

  • 3+ years of team lead experience
  • 5+ years of experience in development with relevant stack
  • Knowledge of microservices architecture, event and component-oriented approaches;
  • Ability to defend decisions reasonably;
  • Customer focus, adequate choice of technical implementation for business needs;
  • Knowledge and understanding of the PLO principles, patterns, understanding the appropriateness of their application;
  • Experience with cloud solutions (Azure - desirable);
  • Understanding of SOLID principles;
  • English (pre-Intermediate or higher);
  • Current .NET stack at disposal:
  • Excellent knowledge of C # and the stack of .net technologies (.Net Core 2.1, Entity Framework Core)
  • Additionally used: Odata Core, Dapper, NSwag, Swashbuckle, Automapper, RabbitMq, Docker, Autofaq, Ninject;
  • Protocols ABAC, RBAC, HTTP, FTP, SSL;
  • Experience with git, jira, confluence;
  • Strong knowledge and experience in working with DBMS (MSSQL, PostgreSql), T-SQL knowledge;
  • Experience in developing web applications and web services (RESTful, microservice approach);
  • Knowledge and experience with js-frameworks (preferable);
  • Experience in TDD (BDD) approach (preferable);
  • English (pre-Intermediate or higher);
  • Excellent oral and written communication skills.

We offer:

  • Challenging job in a highly qualified team;
  • Employee-friendly work environment;
  • Competitive salary;
  • Professional growth in clinical research field
Attach your CV

Key responsibilities

  • Participation in the development, implementation and testing of products;

  • Technical assessment of issues, including alternatives, risk assessment;

  • Participation in the development of project documentation

Requirements

  • 3+ years of development with relevant stack
  • Excellent knowledge of C # and the stack of .net technologies (.Net Core 2.1, Entity Framework Core)
  • Experience with git, jira, confluence;
  • Additionally used: Odata Core, Dapper, NSwag, Swashbuckle, Automapper, RabbitMq, Docker, Autofaq, Ninject;
  • Strong knowledge and experience in working with DBMS (MSSQL, PostgreSql), T-SQL knowledge
  • Experience in developing web applications and web services (RESTful, microservice approach)
  • Knowledge and experience with js-frameworks (desirable)
  • Familiarity with modern design, development and testing methodologies;
  • English (Intermediate and higher);
  • Excellent oral and written communication skills.

We offer:

  • Challenging job in a highly qualified team;
  • Employee-friendly work environment;
  • Competitive salary;
  • Professional growth in clinical research field
Attach your CV

Key responsibilities

  • Development of new projects and support of existing projects on mobile business applications

Requirements

  • experience in commercial development of mobile applications for Android
  • knowledge of Android OS architecture
  • possession of Kotlin language tools
  • experience with HTTP - protocol
  • experience in programming Android services

Preferably

  • iOS development experience
  • knowledge of SQL
  • GIT experience
  • experience with Gradle
  • Excellent oral and written communication skills.

We offer:

  • Challenging job in a highly qualified team;
  • Employee-friendly work environment;
  • Competitive salary;
  • Professional growth in clinical research field.
Attach your CV

Key responsibilities

  • Validation of computer systems;
  • Preparation of validation documentation;
  • Participation in software qualification (IQ, OQ, PQ);
  • Development of additional SOP and work guidelines in accordance with the requirements of ISO 9001: 2008, GMP and GCP;
  • Monitoring еру compliance with the requirements and deadlines for software validation;
  • Participation in company audits.

Requirements

  • Graduate medical / pharmaceutical / biological education
  • Knowledge of GMP, preferably knowledge of GAMP, GCP;
  • English (Upper Intermediate and higher);
  • Experience in pharmaceutical or chemical industry or in clinical research.
  • Excellent oral and written communication skills.

We offer:

  • Challenging job in a highly qualified team;
  • Employee-friendly work environment;
  • Competitive salary;
  • Professional growth in clinical research field.

 

Attach your CV