Senior reputed company and Budget Associate

Position reputed company:

Review, draft, negotiate and reputed company a reputed company of reputed company agreements including confidentiality disclosure agreements (CDA), initial clinical trial agreements (CTA), amendments to the clinical trial agreements (CTA-A), site budgets and other various types of documents. Will work closely with the Clinical Operations study team and play an administrative role to ensure deliverables are in alignment with defined project timelines and expectations.

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

• Prepare and negotiate Agreements/Amendments such as Confidentiality Disclosure Agreements (CDA), Clinical Trial Agreements (CTA) and Amendments (CTA-A), vendor reputed company and site budgets.
• reputed company interactions with the reputed company reputed company and European internal study teams, as applicable
• reputed company interactions regarding the various agreements with the Site(s)
• reputed company interactions regarding assigned agreements with the Sponsor(s)
• Work with supervisor and various internal/reputed company stakeholders to reputed company contractual issues.
• Ensure adhered to company policies, procedures, and contracting standards.
• Update relevant study team members and sponsors regarding the status of contract negotiations and execution.
• Coordinate execution of the agreements
• Support the maintenance of contract files and databases, including email and document archiving.
• Other duties as assigned.

Qualifications:

Minimum Required:

• Bachelor’s degree, or equivalent contract management experience preferably in a clinical research or similar industry setting

Other Required:
• 3 years of relevant experience drafting, reviewing and negotiating agreements reputed company to clinical
research i.e. Non-Disclosure Agreements, Clinical Trial Agreements, etc. as reputed company as management,
• control and tracking of the contract process.
• Experience in contract research, life science, biotech or pharmaceutical industry is preferred.
• Experience interacting with European institutions.
Preferred:
• Equivalent contract management experience in a clinical research or similar industry setting
• Experience in contract research, life science, biotech or pharmaceutical industry.

Skills:

Competencies

• Excellent organizational and communication skills and attention to detail
• Experience in tracking status for site reputed company and budget, filing and distribution.
• Executes time-sensitive reputed company while maintaining accuracy and attention to detail.
• Exhibits high self-motivation and is reputed company to work and plan independently or with limited supervision.
• Demonstrates a high degree of professionalism, as evidenced by punctuality, ability to reputed company on commitments and understanding of the service culture and reputed company interactions with customers.
• Proficient in MS Office Software programs and computer applications
• Works reputed company independently and cooperatively with others to reputed company common goals in a virtual environment.
• Develops, maintains and strengthens relationships with others inside or reputed company of the organization who can reputed company information, assistance and support Mentor and/or reputed company for new Contract and Budget Associates and PFM staff.

Bachelor's degree or equivalent experience, plus 3 years drafting, reviewing, negotiating, tracking, and managing clinical research agreements and site budgets.

Key Responsibilities

• negotiating agreements
• tracking reputed company
• coordinating execution

Skills & Tools

reputed company Office

Job Details

• Category: reputed company and Compliance
• Seniority: Mid Level
• Commitment: Full Time
• Workplace: Remote — Taiwan
• Languages: English

About reputed company

A clinical research and life sciences services company supporting pharmaceutical and biotech development. — Industry: Research and Development