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FSP Manager Clinical Operations

261120303103082303405-000 PPD Global Limited - Istanbul Branch

LocationTurkey
Senioritymid_senior_level
Company261120303103082303405-000 PPD Global Limited - Istanbul Branch
Verified recentlyChecked today
Compensation

Salary not listed

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Requirements and working style

Decision details from the source listing

Experience

5+ years stated

Work authorization

Turkey work authorization

Schedule

fixed

Required overlap

Mon-Fri standard office hours (Turkey time)

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

Mid-senior level Clinical Operations Manager role with 5+ years experience and 1+ year leadership, fully remote option or office in Istanbul, Turkey. Responsible for managing clinical operations team, training, performance management, compliance, and collaboration with senior leadership. Requires solid knowledge of clinical trials, regulations (ICH/GCP, FDA), and leadership skills. Work schedule is standard Mon-Fri office hours.

Role lane

Administrative and data entry, Data, Education, Healthcare admin, Operations, Product, QA and testing, Sales

Where you can work

Turkey

Working hours

Europe/Istanbul

Arrangement

mid_senior_level · full_time

Required signals
clinical operationsclinical trials monitoringleadershipmentoringperformance managementtraining deliveryrisk-based monitoringSOPsWPDsICH/GCPFDA guidelinesmedical research data evaluationcommunication skillsEnglish language
Preferred signals
computer skillsnegotiationorganizational skillsconflict resolutionteam buildingproblem-solvingmedical terminology
Confirm before applying
  • Compensation is not listed
Market context

Administrative and data entry hiring on WFH.team

925active related roles
574new in the latest period
33.2jobs per 100 candidates
$183kmedian of comparable listed ranges

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

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Skills and signals
clinical operationsclinical trials monitoringleadershipmentoringperformance managementtraining deliveryrisk-based monitoringSOPsWPDsICH/GCPFDA guidelinesmedical research data evaluationcommunication skillsEnglish languagecomputer skillsnegotiationFully Remote available with office based in Istanbul, Turkey
Job description

FSP Manager Clinical Operations at 261120303103082303405-000 PPD Global Limited - Istanbul Branch

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as FSP Manager Clinical Operations – Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As a Manager Clinical Operations, you will oversee, train, resource, coach and performance manage a team, which may be inclusive of various clinical operations focused staff. You will focus on end results using metrics and key performance indicators to lead performance. You will act as point-of-escalation regarding performance concerns and training needs to ensure adherence to the company's SOPs and WPDs. You will also work in collaboration with the leadership team for resourcing needs.

DESCRIPTION

What you'll do

  • Manages staff, providing coaching, mentorship and work direction.
  • Conducts regular performance appraisals and career discussions with staff. Facilitates employee career development. Interviews, recruits and selects staff.
  • Manages and conducts induction/orientation programs for all new employees, ensuring their smooth assimilation into the company.
  • Ensures all staff CVs, training records, position profiles and experience profiles are complete and up-to-date. Ensures timeliness and accuracy of timesheets and expense reports.
  • Supports allocation activities per the local resourcing process. Supports activities of project leads/functional leads to optimize the operational running of projects. Raises appropriately any issues which may impact project deliverables.
  • Delivers training on Working Practice Documents (WPDs) and Standard Operating Procedures (SOPs), local requirements and any other subjects that impact on clinical operations. Identifies training gaps and ensures that training requirements are met. May contribute to development of training programs, where appropriate.
  • Assures adherence to good ethical and regulatory standards.
  • Alerts management to quality issues, request QA audits as appropriate, and facilitate client and internal quality assurance audits as required.
  • Handles and reviews systems (e.g. Activate, CTMS, Preclarus, Clarity) to evaluate employee and project metrics, KPIs and general project status.
  • Evaluates work of staff, including conducting PAVs (either remote or on-site) to thoroughly evaluate the employee monitoring skills and project conduction when applicable.
  • Participates in process improvement/development initiatives.
  • Ensures understanding and facilitation of the risk-based monitoring approach.
  • May provide input into bids and contribute to the procurement of new business where required.
  • Collaborates with clinical operations senior management and executive staff on strategic planning and business development as required.
  • May lead or contribute to initiatives that enhance the department's performance or lead to process improvement across the company.

Requirements

Education and Experience Requirements

  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
  • 1+ year of leadership responsibility

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

  • Advanced mentoring/leadership/supervisory skills
  • Excellent clinical trials monitoring skills; Remote and on-site
  • Demonstrated understanding of or ability to learn the company's SOPs, WPDs, and relevant regulations (e.g. ICH/GCP, FDA guidelines)
  • Demonstrated ability to evaluate medical research data
  • Strong organizational and negotiation skills
  • Strong attention to detail
  • Advanced written and oral communication skills
  • Good knowledge of English language and grammar
  • Demonstrated use of computer to include data entry, archival and retrieval
  • Ability to travel as needed
  • Excellent teammate with team building skills
  • Excellent interpersonal and conflict resolution skills
  • Advanced ability to utilize problem-solving techniques applicable to constantly changing environment
  • Solid knowledge of medical/therapeutic areas and medical terminology

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 breakthroughs.