Clinical Project Manager sponsor-dedicated at Fortrea

Istanbul, Istanbul, Turkey -

Full Time

Start Date

Immediate

Expiry Date

22 Feb, 26

Salary

0.0

Posted On

24 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Management, Oncology Expertise, Communication Skills, Negotiation Skills, Financial Management, Analytical Thinking, Teamwork, Organizational Skills, Stakeholder Management, Coaching Skills, Planning Skills, Regulatory Compliance, Clinical Research Knowledge, MS Office Proficiency, Critical Reasoning

Industry

Biotechnology Research

Description

Fortrea is recruiting an experienced Clinical Project Manager with valuable expertise in Oncology. In this role, you will ensure the successful execution of clinical studies on a local level, while maintaining high-quality standards and regulatory compliance. This position is sponsor-dedicated for a renowned pharmaceutical company. Please note this role is for upcoming future opportunities that may arise at Fortrea. Summary of Responsibilities: Leading the local study teams (consisting of monitors and study administrators) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines Ensuring that study sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived Ensuring timely submissions of proper application/documents to Ethic Committee/Regulatory Authority. Close communication with global study teams and overall responsibility for study commitments, for timely delivery of data to required quality as agreed with global Creating and implementing alternative action plans proactively in order to reach the targeted patient numbers; monitoring the patience admission processes in coordination with the researchers; planning and taking the necessary precaution when required Ensuring the compliance of the clinical research process with ICH-GCP practices, the study protocol, Global and Local Clinical SOP’s, and the Ministry of Health Clinical Research Regulations; being knowledgeable about these procedures and keeping abreast of any changes and revision Participating in system/process improvement projects within global and local task groups consisting of employees from different units Qualifications: University degree, preferably from Healthcare related areas (Pharmacy, Veterinary, Chemistry, Biology, Medical etc. Faculties), Advanced level of English, Minimum 5 year experiences in Clinical Research (preferably 2 years in Project Management positions and Oncology specific) Project management skills, Strong communication and negotiation skills, Ability to prioritize and handle multiple tasks, Basic coaching skills and good at team work, Financial management skills, Effective planning and organizational skills with result-oriented approach, Stakeholder management experience, Analytical thinking, critical reasoning ability, Good command of MS Office applications, No restriction to travel, Driving License, Learn more about our EEO & Accommodations request here. Didn’t find what you were looking for? Join our Global Talent Network to stay connected with Fortrea, drive innovation and contribute to our mission of advancing life-saving therapies for patients worldwide. Follow us and stay updated about Fortrea on LinkedIn, Facebook, X, Instagram, YouTube and Glassdoor. At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

Responsibilities

Lead local study teams to ensure the successful execution of clinical studies while maintaining high-quality standards. Ensure compliance with regulatory requirements and timely delivery of data.