Sr. Site Contracts Associate/site Contracts

hace 3 días

Buenos Aires, Argentina IQVIA A tiempo completo

External Job Description

IQVIA Biotech is seeking a Senior Site Contracts Associate or Site Contracts Associate located in Argentina:
**BASIC FUNCTION**:
To manage the review and negotiation of contracts with Investigators participating in clinical research on behalf of pharmaceutical Sponsors.

**ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES**:

- Delivers investigator / institution research-related agreements
- Negotiates clinical trial agreement language and budgets with sites using pre-defined negotiating parameters
- Serves as the primary site contracts lead person for studies
- Prepares and document process flows for each study
- Follows processes that may differ across studies.
- Collaborates with other departments involved in study start-up activities to ensure timely initiation of sites
- Tracks and maintains effective communications with sites and internal staff
- Reports status of Site Contracts to Project Manager and/or Sponsor, as applicable
- Ensures that the site contracts are mutually beneficial contractual agreements for both sites and Sponsor
- Assists supervisor with managing and maintaining contract templates.
- Assists supervisor with management of a team of contract site contracts coordinators for a given study, when applicable
- Performs other duties as assigned.

**KNOWLEDGE, SKILLS, AND ABILITIES**:

- Has advanced knowledge of Intellectual Property issues, Publication issues, Indemnification issues and other standard issues of site contracts within the clinical research area.
- Has Global Site Contracting experience, inclusive of EU.
- Excellent communications skills (verbal and written).
- Ability to negotiate effectively with clients and sites.
- Ability to exercise discretion and judgment while negotiating with clients and sites.
- Must be willing to work in a fast-paced environment with time sensitive material.
- Demonstrated ability to work effectively at all levels of an organization.
- Ability to work independently, prioritize and work in a team environment is essential
- Strong organizational and interpersonal skills.
- Ability to work flexible hours to ensure timelines are met.
- Demonstrated ability to perform multiple tasks effectively.
- Proficient in Excel, Word and Windows
- Willingness and ability to travel (domestically and internationally) as required.

**PHYSICAL REQUIREMENTS**:

- Very limited physical effort required to perform normal job duties.

**MINIMUM RECRUITMENT STANDARDS**:

- Bachelor’s degree (business or law preferred) and 3-5 years of contract analysis and negotiation or related experience in a CRO or pharmaceutical industry
- Equivalent combination of education, training and experience

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