Study Start-Up Analyst (Vicente Lopez, Buenos Aires, AR)
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Department: Clinical Trial Operations, International Operations
Location: Vicente López, Buenos Aires. Hybrid working.
Your impact begins here
As Study Start Up Analyst, you will help clinical trials in Argentina get started on time and the right way. You will prepare and submit the documents that Health Authorities and Ethics Committees need to approve a trial. When your work is accurate and fast, sites can start sooner. That keeps research moving for people living with serious chronic diseases.
What you’ll bring
A university degree in Life Sciences, Pharmacy or a related field.
Experience in regulatory work for clinical trials at a CRO or pharmaceutical company, and hands-on experience with ICH GCP
Experience with trial systems such as CTMS and eTMF
Knowledge of regulatory submissions: local rules, dossier requirements and clinical trial applications
Advanced English.
A sharp eye for detail and the ability to organise and prioritise your work.
Strong communication skills.
A team player mindset.
What you’ll do
You will own start-up and submission activities for your assigned trials, from the first plan to green light – the final approval for a site to start.
Lead and coordinate the preparation, review and submission of Health Authority and Ethics Committee dossiers for your assigned trials, in line with ICH GCP, local regulations and Novo Nordisk processes
Co-develop the start-up plan with Trial Managers and the Trial Start-Up Manager, and plan and track regulatory milestones at country and site level
Adapt, translate and validate key documents – such as informed consent forms, patient materials, labels and clinical trial application documents – including updates requested by authorities
Drive green light activities: collect essential documents, perform quality control, file in eTMF and keep local trial registries and safety submissions up to date
Identify site-level and compliance risks early, act to prevent or mitigate them, and support inspection readiness, audits and inspections
Share local regulatory insights with trial teams and regional and global colleagues, and contribute to improving how start-up and submissions work
Who you’ll work with
You will join Clinical Trial Operations team and report to Adriana Demes, Trial Start-Up Manager. Every day, you will work with Trial Managers and local trial teams.
You will also build strong relationships with trial sites, Ethics Committees, Health Authorities and vendors. Good teamwork here keeps trials on track.
What you can expect here
You will own important work from the start, and your ideas will be heard. You will learn from experts in clinical, regulatory and quality, and build skills that help you grow. We move fast, support each other and never compromise on patient safety or quality.
Start now
Your impact begins today. Apply for the Study Start Up Analyst role by 10 October 2026.
Novo Nordisk is an equal opportunity employer. We welcome applications from all qualified candidates. Every application is considered without regard to gender, gender identity, sexual orientation, age, ethnicity, nationality, religion, disability, marital status or any other characteristic protected by law. If you need adjustments during the recruitment process, let us know.
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Job details
How this role compares
Computed from every other active Clinical Research role in our database, not just this employer's listings.
We currently track 102 comparable Clinical Research roles across 16 biopharma companies.
Salary context
24 of 102 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 102 comparable roles
+ 20 more countries
Seniority mix
65 of 102 peers have a known seniority level
Therapeutic area mix
8 of 102 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.
Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.
Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.
Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.
Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.