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Sr Clinical Project Manager - Turkey - Homebased

Employer
Syneos Health
Location
Istanbul-InonuCadSumerSok, TUR
Salary
Competitive
Start date
26 Sep 2021
Closing date
25 Oct 2021

Job Details

Senior Clinical Project Manager

Sponsor Dedicated

Homebased

Must Haves:

• Demonstrated study management / leadership experience
• Demonstrated oversight of CROs
• Demonstrated experience in managing Per Subject Costs, vendor & ancillary, and monitoring costs projections & spend


Come discover what our 25,000+ employees already know: work here matters everywhere. We're a growing and evolving biopharmaceutical industry leader, which means you'll have endless opportunities to work with experts around the world and build the career you've dreamed of.
As a part of the Syneos Health team, you'll help us deliver results for a rewarding reason - we improve patients' lives around the world. Because to us, a patient isn't just a number, they're our family, friends, and neighbors.

Why Syneos Health
• #SyneosHealthLife means we're committed to our Total Self culture - where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person's unique contributions make a difference.
• We believe our success is a direct result of the people who are driving it - you! We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That's why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong.

Job responsibilities
• Supervise and/or oversee all study-related procedures to ensure they are carried out in accordance with protocol, sponsor's expectations and regulatory guidelines.
• Supervise, coach, and mentor staff and colleagues during clinical conduct of projects.
• Participate in pre-study meeting (Kick-off Meetings, Site Initiation Visits) and Sponsor calls.
• Provide status updates regarding projects to clients and other departments.
• Manage pre-defined study timelines and be proactive in identifying risks and possible solutions to meet critical study milestones.
• Collaborate with other departments to successfully plan and conduct the clinical study.
• Maintain source data throughout the study and perform database cleaning, answering queries and documenting deviations.
• Act as the clinical expert supporting other divisions until completion of the study report.
• Participate in the revision of Standard Operating Procedures (SOPs) and study specific material.
• Ensure on-site files are complete and accurate.
• Coordinate study-monitoring visits, including file review and follow-up of findings/concerns.
• Liaison with the Sponsor or delegate regarding compliance with regulatory requirements and make sure appropriate answers are provided for queries.
• Ensure questions and issues are addressed in a timely manner.
• Act as a resource for study managers and other associates within the company.
• Lead and participate in continuous process improvement projects.
• May manage human capital including workforce planning and hiring activities, performance management and daily monitoring of productivity; facilitate knowledge development and transfer; and ensure the efficiency and mobilization of the team in order to achieve the expected results.What we're looking for
• Bachelor's degree in a related field or equivalent combination of education, training and experience.
• Relative alternate certification may be considered acceptable.
• Six (6) to eight (8) years of relevant experience as a Study Manager, Project Manager within the industry
• English level: Required; includes communicating verbally and in writing on topics that are often technical and writing procedures or technical reports.
• Candidate who does not possess the required training and/or experience may be considered under different criteria.

Get to know Syneos Health
We are the only full-service biopharmaceutical solutions company in the world. That means we bring together the best clinical and commercial minds to create a better, smarter, faster way to get medicines into the hands of patients who need it most. Learn more about Syneos Health.

Additional Information:
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

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