Project Data Manager

Posted 7 Days Ago
Be an Early Applicant
Toronto, ON, CAN
In-Office
Senior level
Biotech • Pharmaceutical
The Role
Lead and manage clinical data management projects end-to-end: delegate tasks, oversee database build/migration, ensure data quality and standards, manage budgets/risks, conduct audits, liaise with stakeholders and vendors, and support DM deliverables including cleaning, reconciliation, and eTMF documentation.
Summary Generated by Built In
Company Description

Medicine moves forward here. So will you. 

Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. We focus on the most complex trials, the studies where experience, judgement, and rigorous operational accountability make the biggest difference. We partner with small to midsize biotech companies to move promising therapies through early phase development, so they reach the patients sooner.  

We choose complex work on purpose. Rare disease and oncology trials carry real operational risk, and our people are experts at reducing it, protecting timelines, data quality and the experience of sites and patients at the same time. It is demanding, meaningful work, and no one here forgets that patients cannot wait. 

That is why culture matters to us as much as capability. We have built a collaborative, international team where people share ideas, grow their careers and are trusted to take ownership early. With colleagues across North America, South America, Europe, Asia and Australia, we value teamwork, flexibility and a real commitment to work-life balance, because good science comes from people who feel supported. 

If you want work with purpose, the agility to make an impact and a team that cares about the people behind the work as much as the work itself, we would love to hear from you. 

 

Job Description

The Project Data Managers (PDM) within the ERGOMED Data Management (DM) department has full responsibility for the successful planning, execution, monitoring, control, and closure of multiple projects. The Project Data Manager represents a position under the direction of the Manager, Data Management.

 

  • Independently lead and delegate tasks to ensure timely completion of project activities to project timelines, quality, and budget 

  • Serve as the primary point of contact for internal teams and external vendors 

  • Conduct internal quarterly audits and ensuring data submission readiness 

  • Manage escalations and study complexities with confidence 

  • Work with PMs to review, forecast budget; ensure study demands / hours / cost / deliverables are in line with budget line items 

  • Provide feedback to other project team members and managers to improve the deliverables 

  • Monitor project risks and implement mitigation strategies 

  • Thorough knowledge of the end-to-end reporting process (data management, statistics, medical writing) 

  • Oversee database build and migration and ensure a quality and timely deliverable 

  • Work with the Lead Data Manager to access data quality issues and develop plans for interim analysis, DRM, DSMB etc. to key stakeholders 

  • Drive adherence to data standards and compliance 

  • Keep abreast of project status and ensure delivery requirements and deadlines are clear and achieved via frequent communication with project teams 

  • Support DM team with key deliverables including documentation creation, finalization, eTMF filing, data cleaning and reconciliation, as required 

 

Qualifications

5 – 8 years’ experience in data management at a pharmaceutical, biotech, or research facility. 

Experience in working with EDC systems (e.g. Merative Zelta, Medrio, Medidata RAVE)

Proficiency in computer applications: Windows, Excel, Word, Outlook etc.

Additional Information

When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.  

We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here. 

  • Quality: we hold ourselves to the standard patients deserve. 

  • Integrity and trust: we do the right thing, especially when it is hard. 

  • Drive and passion: we care about the outcome, because someone is waiting on it. 

  • Agility and responsiveness: we move quickly, because patients cannot wait. 

  • Belonging: everyone is welcome, and every voice counts. 

  • Collaborative partnerships: we go further by going together. 

We look forward to welcoming your application. 

#LI-Remote

Skills Required

  • 5-8 years experience in data management at a pharmaceutical, biotech, or research facility.
  • Experience working with EDC systems (Merative Zelta, Medrio, Medidata RAVE).
  • Proficiency with computer applications (Windows, Excel, Word, Outlook).
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
HQ: London
535 Employees
Year Founded: 1997

What We Do

Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology. • 1,400+ highly qualified professionals • Global full-service CRO • 25+ years of experience • Therapeutic specialization in oncology • Strong expertise in rare disease trials • Robust clinical safety system • Choice of leading drug safety databases Our key services include: • Clinical Research Services • Pharmacovigilance • Medical Information • Regulatory • Medical Writing • Site Management • Study Physician Support • Biostatistics • Patient Study Support

Similar Jobs

Magna International Logo Magna International

Shipping/Receiving Materials Attendant

Automotive • Hardware • Robotics • Software • Transportation • Manufacturing
Hybrid
Brampton, ON, CAN
171000 Employees
25-31 Hourly

Magna International Logo Magna International

Manufacturing Engineer

Automotive • Hardware • Robotics • Software • Transportation • Manufacturing
Hybrid
Milton, ON, CAN
171000 Employees
61K-73K Annually

Magna International Logo Magna International

Manufacturing Engineering

Automotive • Hardware • Robotics • Software • Transportation • Manufacturing
Hybrid
Milton, ON, CAN
171000 Employees
85K-105K Annually

TransUnion Logo TransUnion

Batch Analyst (13-month Maternity Leave Contract)

Big Data • Fintech • Information Technology • Business Intelligence • Financial Services • Cybersecurity • Big Data Analytics
Hybrid
Burlington, ON, CAN
13000 Employees

Similar Companies Hiring

SOPHiA GENETICS Thumbnail
Software • Healthtech • Biotech • Big Data • Artificial Intelligence
Boston, MA
450 Employees
Pfizer Thumbnail
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
New York, NY
121990 Employees
Cencora Thumbnail
Healthtech • Logistics • Pharmaceutical
Conshohocken, PA
51000 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account