drjobs Sr Site Contracts Specialist (Israel) العربية

Sr Site Contracts Specialist (Israel)

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

Tel Aviv - Israel

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research development and delivery of life-changing therapies. With clinical trials conducted in 100 countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio our work spans laboratory digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future.

Our global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out across commercial and government contracts. Together we help clients define and develop clinical programs minimize delays and implement high-quality cost-efficient clinical studies.

Discover Impactful Work:

Manages the preparation discussion and finalization of the contracts process. Liaises and establishes effective relationships with sites and internal functional teams. Ensures quality objectivity and risk analysis in the efficient delivery of Investigator Contracts. May mentor junior staff.

A day in the Life:

  • Drafts reviews negotiates and finalizes agreements with study sites in accordance with local/accepted process.
  • Negotiates within approved parameters both investigator grant budget consultation parameters contractual terms and conditions in accordance with Company contractual considerations client contractual considerations established process with sites and follows established escalation routes.
  • Ensures compliance to established mediation parameters authority approval contractual process and client expectations.
  • Ensures compliance of budgetary guidance templates and process.
  • Identifies and assesses legal financial and operational risks in accordance with company and client contractual considerations and escalates to appropriate level of the organization per established processes.
  • Provides recommendations and alternative resolutions to Investigator Contracts discussions through established escalation channels.
  • Coordinates with internal functional departments to ensure various site startup activities are aligned with contractual activities and mutually agreed upon timelines; ensures alignment of contract dialogue process for sites and study are properly aligned to the critical path for site activation.
  • Achieves target cycle times for site activations.
  • Ensures guidelines and processes are followed for efficient escalation of out of parameter issues as applicable.
  • Completes tracking and reporting as required.
  • May provide training and mentoring to junior staff.
  • Participates in country process improvement initiatives representing Global Site Contract activities within country team meetings.
  • Acts as country subject matter expert in review of Investigator Contracts training materials.
  • Liaises with Global Site Contracts to ensure full compliance with established global processes and corporate directives.
  • Completes periodic quality reviews and peer feedback reports.
  • May act as lead with amendment/novation client projects and oversight of confidentiality agreement negotiations.
  • Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors.
  • A seasoned experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways. This job is the fully qualified dedicated journey-level position.
  • Normally receives little instruction on day-to-day work general instructions on new assignments.
  • Demonstrates good judgment in selecting methods and techniques for obtaining solutions.
  • Represents the department as a prime contact on projects.
  • Interacts with internal and external personnel on significant matters often requiring coordination between functional areas.
  • Networks with senior internal and external personnel in own area of expertise.

Keys to Success:

Education

  • Bachelors degree or equivalent and relevant formal academic / vocational qualification

Experience

  • Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 5 years).
  • 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 Abilities

  • Detailed understanding of the principles of contract law including a general understanding of laws that influence contract language such as business intellectual property and local tax and stamp laws
  • Effective communication skills (verbal & written) in English and local language
  • Detailed understanding and demonstrated ability to effectively mediate investigator grant budgets within parameters
  • Demonstrated skill in strong attention to detail
  • Excellent analytical and decision based thinking skills
  • Solid knowledge and understanding of the pharmaceutical product development process and involvement of CROs
  • Able to work independently or in a team environment
  • Good organizational and time management skills
  • Solid understanding of PPD SOP & WPDs
  • Able to organize competing priorities logically and review outstanding contractual risk and issues
  • Able to effectively use automated systems and computerized applications
  • Ability to demonstrate a customer focused style of communication problem solving and collaboration
  • Detailed understanding of the principles of contract law including a general understanding of laws that influence contract language such as business intellectual property and local tax and stamp laws
  • Detailed understanding and demonstrated ability to effectively negotiate investigator grant budgets within negotiation parameters
  • Demonstrated ability to independently train and mentor staff
  • Demonstrated ability to provide valuable feedback to Investigator Analysts
  • Strong problem solving skills that are demonstrated via solid risk analysis that results in resolution or escalation as appropriate
  • Demonstrated ability to effectively negotiate Investigator Contracts in the best interests and position of the company and client

Working Environment

Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

  • Able to communicate receive and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
  • Able to work upright and stationary for typical working hours.
  • Ability to use and learn standard office equipment and technology with proficiency.
  • Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
  • May require travel. (Recruiter will provide more details.)


Required Experience:

Senior IC

Employment Type

Full-Time

Company Industry

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.