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Regulatory Affairs Manager (Global Clinical Trial Applications)

PPD Italy S.r.l

LocationSerbia
Senioritymid_senior
CompanyPPD Italy S.r.l
Verified recentlyChecked today
Compensation

Salary not listed

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Requirements and working style

Decision details from the source listing

Experience

9+ years stated

Education

Bachelor's degree or advanced degree preferred or equivalent formal academic/vocational qualification

Work authorization

Work authorization for Serbia

Schedule

fixed

Required overlap

Standard (Mon-Fri)

Benefits stated
Competitive salaryExtensive benefits package focused on health and well-beingFlexible working cultureWork-life balance valuedCollaborative global environmentOpportunities for growth and development

These fields are normalized from the employer's text. Confirm details on the employer site before applying.

WFH.team analysis

What this posting tells you

Regulatory Affairs Manager position at PPD Italy S.r.l for managing global clinical trial applications with mid-senior level experience (9+ years) in regulatory affairs and project management. The role is remote and based in Serbia with standard business hours (Mon-Fri). Requires relevant degree and strong knowledge of global/regional regulatory requirements. Employment types include contract and full-time. Salary is not specified.

Role lane

Education, Finance and investments, Healthcare admin, Marketing, Product, Sales, Security, Customer support, Writing and content

Where you can work

Serbia

Working hours

Europe/Belgrade

Arrangement

mid_senior · contract · full_time

Required signals
Regulatory AffairsRegulatory StrategyProject ManagementClinical Trial ApplicationsBudgetingForecastingClient-facing Communication
Preferred signals
Microsoft WordMicrosoft ExcelMicrosoft PowerPointNegotiation Skills
Confirm before applying
  • Compensation is not listed
Market context

Education hiring on WFH.team

3,718active related roles
2,426new in the latest period
3442.6jobs per 100 candidates
$155kmedian of comparable listed ranges

Category counts come from WFH.team's latest published remote job market snapshot.

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Skills and signals
Regulatory AffairsRegulatory StrategyProject ManagementClinical Trial ApplicationsBudgetingForecastingClient-facing CommunicationMicrosoft WordMicrosoft ExcelMicrosoft PowerPointNegotiation SkillsRemote / Fully Remote
Job description

Regulatory Affairs Manager (Global Clinical Trial Applications) at PPD Italy S.r.l

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life—enabling our customers to make the world healthier, cleaner and safer. With clinical trials conducted in 100+ countries and ongoing development of innovative frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.

We are currently seeking a Regulatory Affairs Manager to join our global Regulatory Affairs department, Regulatory Science team. This is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting.

In this role, you will be part of a global team providing innovative regulatory solutions, owning regulatory affairs responsibilities, and leading discussions with internal and external clients. You will coordinate global regulatory strategies on assigned (Phase 1–4) clinical trials, studies, and projects, supporting clients with strategic regulatory intelligence and guidance throughout clinical development.

Role Focus at This Level

  • This position sits within our senior individual contributor framework
  • In this Manager role, the emphasis is on oversight across multiple projects, client engagement, and accountability for delivery, scope, and financial elements .

Responsibilities

  • Lead the preparation of global regulatory submissions for CTA and ensure high quality standards that meet local and regional requirements.
  • Act as subject matter expert in providing regulatory strategy advice and technical expertise to internal and external clients and for key client projects of moderate to high complexity.
  • Provide oversight across multiple studies/projects , ensuring alignment of regulatory strategy, quality, and delivery.
  • Act as a senior client-facing lead , contributing to broader regulatory planning and supporting proposals, bid defenses, and scope discussions.
  • Ensure quality performance for key/managed projects.
  • Manage project budgeting/forecasting functions and maintain accountability for financial and scope management .
  • Identify and recognize out-of-scope activities and partner with relevant teams to manage contract modifications.
  • Collaborate with business development in pricing and securing new business by contributing to proposals, budgets, and client presentations.
  • Provide matrix/project leadership and guidance to team members.
  • Ensure compliance with relevant organizational and regulatory SOPs and WPDs.
  • Participate in launch meetings, review meetings, and project team meetings.

Qualifications

Education and Experience

  • Bachelor’s degree or advanced degree preferred, or equivalent and relevant formal academic/vocational qualification
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 9+ years)
  • Proven project management experience and experience performing effectively in a client-facing role

Knowledge, Skills and Abilities

  • Strong understanding of global/regional regulatory requirements and ICH guidelines
  • Excellent analytical, investigative, and problem-solving skills
  • Solid understanding of budgeting and forecasting
  • Excellent English language (written and oral) communication skills as well as local language where applicable
  • Excellent attention to detail and quality, with strong editorial/proofreading skills
  • Exceptional interpersonal skills to work effectively in a team environment and act as a liaison with other departments
  • Advanced computer skills including Microsoft Word, Excel, and PowerPoint
  • Strong organizational, time management, and planning skills
  • Excellent negotiation skills

What We Offer

As well as being rewarded with a competitive salary, we offer an extensive benefits package focused on health and well-being. We provide a flexible working culture where work-life balance is valued, alongside a collaborative global environment with opportunities for growth and development.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. As one team of 100,000+ colleagues, we share a common set of values—Integrity, Intensity, Innovation, and Involvement—working together to accelerate research and support patients in need.

#LI-AS3

Company context

Working remotely at PPD Italy S.r.l

PPD Italy S.r.l is hiring for 2 active remote roles, with remote-friendly openings, application links, and job details refreshed from the public remote job inventory.

Remote policy

Remote hiring signal is inferred from active confirmed-remote job listings.

Research PPD Italy S.r.l
Remote Regulatory Affairs Manager (Global Clinical Trial Applications) at PPD Italy S.r.l | WFH.team