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Freelance project manager Jobs in Levis qc

Last updated: 14 hours ago
  • Promoted
Regulatory Project Manager

Regulatory Project Manager

Syneos HealthQuebec City, QC, Canada
Full-time
Show moreLast updated: 20 days ago
Project Manager

Project Manager

Alpe ConceptionQuebec
Show moreLast updated: 30+ days ago
Project manager

Project manager

St-AmourLaurentians
CA$120,000.00 yearly
Permanent
Show moreLast updated: 30+ days ago
Electrical Project Manager

Electrical Project Manager

Bedard RessourcesLevis, Quebec, Chaudiere-Appalaches
CA$80,000.00–CA$90,000.00 yearly
Permanent
Show moreLast updated: 30+ days ago
  • Promoted
Project Manager - Construction

Project Manager - Construction

Borea Construction, Québec, CA
Full-time
Quick Apply
Show moreLast updated: 5 days ago
Project Manager

Project Manager

EightSix NetworkQC
CA$32.00–CA$42.00 hourly
Show moreLast updated: 30+ days ago
Project Manager, Automatisation

Project Manager, Automatisation

CreaformCanada - Levis
Show moreLast updated: 26 days ago
  • Promoted
  • New!
Work from Home Chemistry Expertise Sought for AI Training

Work from Home Chemistry Expertise Sought for AI Training

OutlierQuebec City, Quebec, Canada
CA$30.00–CA$50.00 hourly
Remote
Full-time
Show moreLast updated: 14 hours ago
Site Project Manager

Site Project Manager

ActalentQuébec City, Quebec, Canada
CA$31.00–CA$48.00 hourly
Show moreLast updated: 30+ days ago
Project Manager - Buildings

Project Manager - Buildings

PomerleauLévis, Québec, CA
Show moreLast updated: 30+ days ago
Technical Project Manager

Technical Project Manager

Big Fish GamesQuebec, QC, CA
CA$500.00 weekly
Full-time
Show moreLast updated: 30+ days ago
Project Manager

Project Manager

HITACHI ENERGY CANADA INC.Quebec, Quebec, Canada
CA$60.00 hourly
Full-time
Show moreLast updated: 30+ days ago
Project Manager

Project Manager

CT Real EstateQuebec
Full-time
Show moreLast updated: 30+ days ago
Project Manager / Gestionnaire de projet

Project Manager / Gestionnaire de projet

First Onsite - CAQuebec, QC, CAN
CA$32.00–CA$42.00 hourly
Full-time
Quick Apply
Show moreLast updated: 30+ days ago
Project Manager

Project Manager

CS GROUPQC, ca
CA$120,000.00–CA$150,000.00 yearly
Show moreLast updated: 30+ days ago
  • Promoted
Project Manager

Project Manager

Jump! RecruteursQuebec City, QC, Canada
Full-time +1
Show moreLast updated: 19 days ago
  • Promoted
Office Manager Freelance (Gestion administrative et comptabilité)

Office Manager Freelance (Gestion administrative et comptabilité)

freelance.caQuebec, Canada
CA$40.00–CA$50.00 hourly
Full-time
Show moreLast updated: 18 days ago
ERP Project Manager

ERP Project Manager

DELAN - IT Head HuntersAnywhere - Quebec
CA$180,000.00 yearly
Show moreLast updated: 30+ days ago
Senior Project Manager

Senior Project Manager

JumpQuebec, Canada
Full-time
Show moreLast updated: 30+ days ago
HVAC Project Manager

HVAC Project Manager

Le Groupe MasterQuébec
CA$100,000.00 yearly
Show moreLast updated: 30+ days ago
Regulatory Project Manager

Regulatory Project Manager

Syneos HealthQuebec City, QC, Canada
20 days ago
Job type
  • Full-time
Job description

Description

Regulatory Consultant

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know :

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

  • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
  • We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
  • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we’re able to create a place where everyone feels like they belong.

JOB RESPONSIBILITIES

  • Conduct research of existing product data relative to global or regional regulatory requirements for the preparation of gap analyses, product development plans, and other regulatory submissions.
  • Contribute to or prepare administrative and technical components of regulatory agency submissions for the IND, for pre-approval submission packages, for product registration applications, and for post-approval maintenance. Prepare briefing packages for regulatory agency meetings or scientific advice and contribute to or support the agency interactions.
  • Manage and / or operationalize the delivery of day-today regulatory activities for assigned project according to agreed timelines, scope of contract, budgets, and strategies.
  • Participate as regulatory support on multidisciplinary project teams, which may include clinical and other technical experts, to develop products throughout their life cycle.
  • Act as a subject matter expert and help the team members with day-to-day trouble shooting activities, presenting solutions to project related problems.
  • Prepare estimates for conducting regulatory services as part of single or multiple service proposals.
  • Support meetings with clients to discuss proposals, the status of ongoing projects, and as part of general business development activities.
  • Ensure compliance with appropriate global regulatory requirements and the company’s policies and processes.
  • Prepare training materials and share best practices in the regulatory area, both internally and externally.
  • Participate as regulatory support in internal or external project audits.
  • Participate as regulatory support on internal cross-functional initiatives.
  • Contribute to the creation and / or maintenance of SOPs and other process related documentation
  • as required.

  • Provide support in oversight to team members in the execution of their project responsibilities.
  • Capable of identifying when to ensure line support required to provide additional guidance and
  • direction.

  • Maintenance of individual training records (Syneos Health or client related) and completion of all designated required training.
  • Qualifications

    What we’re looking for

  • BS or PhD degree, preferably in a science-related field or equivalent experience in science / regulatory / medical writing-related field. Moderate pharmaceutical / medical device related experience.
  • Demonstrated experience in contributing to the preparation of regulatory submissions including, for example IND, PMA, NDA, MAA, and CTD, including electronic submissions.
  • Excellent interpersonal / communication skills including excellent written and verbal communication skills.
  • Excellent customer service skills, with the ability to work both as a team member and independently.
  • Good quality management skills.
  • Advanced skills in Microsoft Office Applications.
  • Ability to interact with staff from multiple departments and offices to establish project standards.
  • Good initiative, adaptability, and pro-activity.
  • Strong analytical skills, good attention to detail.
  • Ability to work concurrently on projects, each with specific instructions that may differ from project to project.
  • Fluent in speaking, writing, and reading English.
  • Get to know Syneos Health

    Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

    No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

    Additional Information :

    Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and / or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills / experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.