Precision Medicine Group
Precision Medicine Group

Site Contracts Manager (Türkiye)

TLDR

The role involves reviewing, drafting, and negotiating a wide range of legal agreements while ensuring compliance with Turkish regulations and managing contract metrics.

Precision for Medicine is growing! We are looking for a Site Contracts Manager to join our team in Turkey. This position requires expertise in Turkish legal requirements, paired with substantial site contract and budget negotiating experience and expertise. Position can be covered fully remotely from Turkey.

Position Summary:

Review, draft, negotiate and track a variety of legal agreements including confidentiality agreements, master confidentiality agreements, clinical study agreements and amendment agreements. Work closely with Clinical Operations study team and play a key role to ensure deliverables are in alignment with defined study timelines.

Essential functions of the job include but are not limited to:

  • Review, draft and negotiate site contracts, and possible a variety of other agreements, including master services agreements, consulting agreements, vendor agreements, confidentiality agreements, and other contracts.
  • Work with supervisor and various internal/external key stakeholders to resolve/escalate contractual issues.
  • Ensure adherence to company policies, procedures and contracting standards.
  • Update relevant study team members regarding the status of contract negotiations and execution.
  • Establish, track, report and manage site contract metrics.
  • Support the maintenance of contract files and databases, including contract archiving.
  • Assist in designing and implementing policies and procedures to affect the timely execution of contracts.
  • Recognize where processes can be improved and take corrective action.
  • Other tasks as assigned.

Qualifications:

Minimum Required:

  • Fluent Turkish and English
  • Graduate, postgraduate, 4-year college degree
  • Experience in a CRO or on clinical site's side
  • Relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations, but no less than 5 years’ experience.
  • Substantial experience in site contract and budget negotiation in Turkey, with expertise in Turkish local requirements ( experience related to any other country and/or region is considered a strong plus)
  • Experienced leading interactions with Study Teams

Preferred:

  • Bachelors in law, scientific fields, business administration or equivalent degree
  • Excellent organizational and communication skills and attention to detail
  • Knowledgeable on setting up Contracting Plans - Guides for CTA & Budget negotiations
  • Successful handling relationship study team and/or with CRAs/Start-up Associate/(S)BSCA to meet study timelines
  • Experienced leading interactions with Sponsors

Skills and Competencies:

  • Possesses strong organizational/written communication skills and the ability to multi-task and prioritize in a fast-paced environment.
  • Executes time-sensitive matters while maintaining accuracy and attention to detail.
  • Exhibits high self-motivation and is able to work and plan independently as well as in a team environment.
  • Demonstrates a high degree of professionalism, as evidenced by punctuality, ability to deliver on commitments, an understanding of the service culture and positive interactions with customers and teammates, including good interpersonal skills.
  • Displays sound business judgment and a proactive, independent work style.
  • Proficient in MS Office software programs and computer applications.
  • Handles sensitive issues with discretion.
  • Works well independently and cooperatively with others to achieve common goals in a virtual environment.
  • Develops, maintains, and strengthens relationships with others inside or outside of the organization who can provide information, assistance, and support.

#LI-Remote

#LI-TB1

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Precision Medicine Group is a specialized contract research organization (CRO) focused on precision medicine, aiding pharmaceutical and life sciences companies in innovating, developing, and commercializing advanced medical products. With a unique blend of novel clinical trial designs, operational expertise, and advanced biomarker solutions, they concentrate on solving challenges in rare diseases and oncology.

Founded
Founded 2012
Employees
201-500 employees
Industry
Pharmaceuticals
View company profile
Report this job
Apply for this job