Join OncoDNA Team

We are always looking for new talents to join the team. If you are ready for new exciting challenges, contact us !

IT Project and Team Manager New

Belgium

Description :

Project managers have the responsibility of the planning, procurement and execution of a project. Team management involves teamwork, communication, objective setting and performance appraisals. Moreover, team management is the capability to identify problems and resolve conflicts within a team.


Your mission :

A project manager is the person responsible for accomplishing the project objectives:

  • Defining and communicating project objectives that are clear, useful and attainable
  • Procuring the project requirements, required information, various agreements and material or technology needed to accomplish project objectives
  • Managing the constraints of the project management: cost, time, scope and quality

Main technologies/methodologies we use are :
  • Django for web apps in the backend
  • AngularJS in the frontend
  • Agile methodologies

Education :
  • Bs or Ms in computer science

Experience :
  • More than 7 years in Project and team Management
  • More than 7 years as a Python developer or equivalent (Ruby, PHP, ...)
  • Experience in developing (web) applications
  • Certification as Scrum master/PRINCE2 is a plus
  • Experience in the Health industry is a plus

Skills :
  • Project Management
  • Team Management
  • Python
  • SQL - NoSQL

Personal Skills :
  • Self starter who enjoys making things simple
  • You’re passionate about Health industry
  • Eager to learn new stuff everyday, including by yourself
  • Share knowledge and experience with the dev team
  • You’re a good listener
  • You know how to effectively lead a growing a team

Interested ?

Interested to work with us ? Send your CV and cover letter at this email address gregori.ghitti@oncodna.com.

IT

Full-Time

Clinical Data Manager New

Belgium

Company information

OncoDNA, the Cancer Theranostic Company is based in Belgium (Gosselies). Our main service is called OncoSTRAT&GO and aims to provide oncologists with treatment options based on a comprehensive molecular characterization of the tumor. We translate the findings of these analyses into cancer treatment options/ recommendations and we provide physicians not only with a list of approved drugs and compounds under development which best fit patients’ specific condition but also with a list of the clinical trials available for the patient according the specificity of his/her tumor.


Your mission :
  • Provide Clinical data management support to Clinical Operations team and/or study project, Clinical Data Management team and Biostatistics team.
  • Participates in the review of Clinical research documents (eg. Protocols, Case Report Forms, Reports and Statistical analysis).
  • Develops Data Management Plan (DMP), maintains DMP throughout lifecycle of study project and ensures DMP is followed according to study design and requirements.
  • Develop Case Report Form (CRF), electronic and/or paper.
  • Develop database (DB) clinical trial data specifications, including eCRF design, user requirements, edit rules/checks, query logic and data validations.
  • Lead EDC database (DB) specification process
  • Develops Data Transfer Agreement(s) (DTAs) between external data vendors and/or core labs.
  • Reconcile electronic data transfers from vendor to Sponsor.
  • Develop test scripts and execution logs for User Acceptance Testing (UAT).
  • Coordination of UAT of eCRF build and validation documents, included but not limited to: edit check document, issue logs, UAT summary report.
  • Maintenance/tracking of EDC user management and other Clinical databases across allocated Clinical trials, including but not limited to, compiling master user lists and activating/deactivating user accounts.
  • Perform training on study trial for EDC and create user guides .
  • Ensure clinical data within EDC is in quality to lock/unlock and freeze/unfreeze as appropriate for statistical review, interim review, and or final database lock- included but not limited to: data reconciliation and/or coding.
  • Assist in defining and/or create data listings, summary table validation, data specifications and/or process data transfers in preparation for statistical review and/or data management audit.
  • Coordinate the archiving of study databases and related documents.
  • Perform close-out audit, as specified, for closing of study trial in EDC or other clinical data management DBs.
  • Assist in reconciling AE/SAE data in Safety DB and/or other Data Management DB, including but not limited to, performing MedDRA and/or WHO coding.
  • Assist and provide input into study and project level data analysis plan.
  • Coordinate and communicate with DB vendors on consistent basis to address Clinical teams requests, project plans, and/or eCRF development activites.
  • Collaborate with IT and implementation team(s) to address Clinical application requests and/or changes to Clinical database systems.
  • Participates in the preparation and presentation of data, when applicable. • Ensures data system compliance by following the established guidelines of national and international regulatory authorities.
  • Participate in conference calls and/or meetings with vendors .

Your Profile :
  • (Para)medical or scientific degree
  • Minimum 1 year CRA or Study Coordinator experience
  • Knowledge and experience in international standards (GCP/ICH), international (FDA, EMA) and local regulations
  • Team player, strong interpersonal skills
  • Proven expertise in effective communication, in managing multiple priorities and in computer literacy
  • Able to work independently within your area of responsibilities
  • An eye for detail and affinity with administration, meticulous and quality-minded
  • Fluent English (German would be one more)
  • Advanced computer skills
  • Driver’s license B

Interested ?

Interested to work with us ? Send your CV and cover letter at this email address jf.laes@oncodna.com.

Scientific

Full-Time

Clinical Research Associate New

Belgium

Description

As a Clinical Research Associate (CRA) you are the main communication link between OncoDNA company and the investigational staff. You coach the site throughout the clinical study and make sure that it is conducted in accordance with all applicable guidelines.


Your mission :
  • Write the clinical trial protocol and all the associated documents.
  • Perform monitoring visits from initiation to close out.
  • You may support in operational feasibility to assess feasibility.
  • Ensure detailed corresponding reports and administration.
  • Train your investigational site staff on study specific procedures.
  • Evaluate appropriate site compliance and data quality.
  • Reconcile electronic data transfers from vendor to Sponsor.
  • Respond to site-related queries and escalate site-related issues.
  • You are responsible for operational site management.
  • You actively contribute to results oriented department goals.

Your Profile :
  • (Para)medical or scientific degree
  • Minimum 1 year CRA or Study Coordinator experience
  • Knowledge and experience in international standards (GCP/ICH), international (FDA, EMA) and local regulations
  • Team player, strong interpersonal skills
  • Proven expertise in effective communication, in managing multiple priorities and in computer literacy
  • Able to work independently within your area of responsibilities
  • An eye for detail and affinity with administration, meticulous and quality-minded
  • Fluent English (German would be one more)
  • Advanced computer skills
  • Driver’s license B

Interested ?

Interested to work with us ? Send your CV and cover letter at this email address jf.laes@oncodna.com.

Scientific

Full-Time

You Want to Know More?

Send us an email at jonathan.lecocq@oncodna.com with a complete curriculum vitae and cover letter.
We'll contact you as soon as possible and make an appointment.