Part-Time Domestic Helper
Deborah Macan Markar
Job type full-time
Full job description
Laval, qc, canada montreal, qc, canada virtual req #1355
Friday, march 5, 2021
Altasciences is a mid-size contract research organization with a unique focus on supporting drug development from lead candidate selection to proof of conceptWith over 25 years of industry experience, we provide preclinical and clinical solutions to an international customer base of biopharmaceutical companiesOur full-service offering in this critical stage of drug development includes program management, preclinical safety testing, clinical pharmacology services, manufacturing and analytical services, medical writing, biostatistics, data management, and bioanalysis services tailored to specific research requirementsAltasciences has facilities in montreal, qc; kansas city, ks, seattle, wa, and philadelphia, pa.
Our team is made up of over 1,300 professionals from the medical and scientific fields who work together to
Achieve a common goal: to contribute to the advancement of life sciencesBring your talents and forward-thinking approach to altasciences and help us develop medicines for those who need them, faster.
You want to make a difference by helping to improve people's quality of life? our opportunity will surely interest you! as a fast-growing contract research organization, you will have the opportunity to develop your skills and advance in your careerIf you stand out for your organizational skills, your attention to detail and teamwork; don't hesitate to send us your resume!
The administrative assistant is responsible for producing regulatory submissions of the highest quality standards, in compliance with ich and regional format requirementsHe/she is working closely with associates across departments at altasciences and he/she is accountable for the timely delivery of regulatory submissions that meet both internal and external electronic format requirements.
Ensure regulatory documents are properly assembled and formatted as per requirements for electronic submissions & internal standards;
Ensure submission structures produced meet internal specifications as defined by the external clients;
Ensure submission attributes consistently comply with regional and ich specifications for regulatory submissions;
Accountable for the timely completion of all deliverables requested by internal clients (other internal departments);
Properly manage personal timelines and workload distribution between short term and long term deliverables such that all project deadlines are respected;
Deliver regulatory submissions in the proper format as specified in the internal client requests (from other regulatory departments at altasciences);
Other related tasks.
Ideally a college degree in science or in a relevant disciplineOne (1) to three (3) years of pertinent experience may be considered in lieu;
Bilingualism (french/english) written and spoken are essential;
Knowledge of the pharmaceutical industry is an asset;
Meticulous, strict attention to detail;
Strong team spirit and sense of customer service;
Ability to multitask in a fast-paced environment;
Ability to work under pressure and tight timelines;
Fast learner with proven ability to adapt to changing demands;
Highly functional and comfortable with computer applications, ms-office and adobe pro.
Altasciences is an equal opportunity employer committed to diversity and inclusionOur goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectivesAll qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislationReasonable accommodations for persons with disabilities during the recruitment process are available upon requestJoin us at altasciences!