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Medical Project Coordinator, EMEA

PPD Serbia D.O.O

LocationMexico, Serbia
Senioritymid-level
CompanyPPD Serbia D.O.O
Verified recentlySep 21
Compensation

Salary not listed

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Requirements and working style

Decision details from the source listing

Experience

2+ years stated

Education

Bachelor's degree in nursing or related Health Sciences (Physician's Assistant) or licensed RN

Schedule

fixed

Required overlap

Mon-Fri standard hours

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

Medical Project Coordinator role supporting drug safety operations with focus on clinical trials compliance and patient safety. The position is fully remote with locations in Mexico and Serbia. Requires a Bachelor's degree in nursing or related Health Sciences and at least 2 years clinical safety experience including pharmacovigilance or clinical research monitoring. Work schedule is standard Monday to Friday office hours.

Role lane

Customer success, Data, Education, Healthcare admin, Medical billing, Operations, Patient support, Product, Sales, Security, Customer support

Where you can work

Mexico, Serbia

Working hours

Timezone overlap is not stated.

Arrangement

mid-level · contract · full_time

Required signals
DataGCPGoMedicalOperationsSupportclinical safety experiencepharmacovigilanceclinical research monitoring
Preferred signals
biostatisticsdata managementclinical proceduresproblem solvingcritical thinkingcommunication skills
Confirm before applying
  • Required timezone overlap is not stated
  • Compensation is not listed
Market context

Customer success hiring on WFH.team

6,217active related roles
3,951new in the latest period
2558.4jobs per 100 candidates
$129kmedian of comparable listed ranges

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

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Skills and signals
DataGCPGoMedicalOperationsSupportclinical safety experiencepharmacovigilanceclinical research monitoringbiostatisticsdata managementclinical proceduresproblem solvingcritical thinkingcommunication skillsFully Remote
Job description

Medical Project Coordinator, EMEA at PPD Serbia D.O.O

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join us as Medical Project Coordinator – And utilize your expertise to support and enhance drug safety operations, ensuring compliance with regulatory standards and optimal patient safety in clinical trials.

What you’ll do

  • Coordinate and review safety data, utilizing line listings, company dashboard(s) and/or other visualization tools. Review data for safety trends,

coding consistencies, and potential follow up with investigator sites. Identify potential issues and resolve or escalate as appropriate.

  • Review safety data and may provide summations for safety review meetings.
  • May review designated sections of aggregate reports.
  • May help to create/review safety and medical management plan(s) on studies (as applicable) and ensures that the processes included in plan documents are reflective of the contract and services requested.
  • May help manage routine project implementation, forecasting and coordination, including review of metrics and budget considerations.
  • Monitor the status of the data review and escalate any delays and/or risks to all stakeholders, including study leads.
  • May present at business development, client, and investigator meetings and participate in strategy/business development calls.
  • Resolve complex problems through in-depth evaluation of various factors and offers solutions.
  • May serve as the primary point of contact for clinical/data management project teams.
  • May assist management in training and mentoring.

Education and Experience

  • Bachelor’s degree in nursing or related Health Sciences (Physician's Assistant) or licensed RN
  • Previous experience to provide the knowledge, skills, and abilities to perform the job (comparable to 2+ years), to include 2+ years clinical safety experience (clinical research monitoring, or pharmacovigilance or combination of clinical research monitoring and pharmacovigilance)

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities

  • Knowledge of GCPs for medical oversight of clinical trials and SAE processing
  • Knowledge of drug development and safety reporting
  • Knowledge of safety data trending to include coding
  • Working knowledge of biostatistics, data management and clinical procedures
  • Strong problem solving and critical thinking skills
  • Good oral and written communication skills
  • Good attention to detail
  • Ability to work in a collaborative team environment
  • Ability to maintain a positive and professional demeanor in challenging circumstances

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthrough.

Company context

Working remotely at PPD Serbia D.O.O

PPD Serbia D.O.O is hiring for 3 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.

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Remote Medical Project Coordinator, EMEA at PPD Serbia D.O.O | WFH.team