Senior Site Identification and Relationship Manager - US/Mexico City/Argentina - Remote
Worldwide Clinical Trials
Summary
The Site Identification and Relationship manager will primarily support post-award Site Identification activities, including development of site identification strategies, feasibility questionnaire management, CDA and outreach coordination, site recommendation activities, training of assigned resources, and oversight of Site Activation Specialist support resources.
Job description
What you will do
The Site Identification and Relationship manager will primarily support post-award Site Identification activities, including development of site identification strategies, feasibility questionnaire management, CDA and outreach coordination, site recommendation activities, training of assigned resources, and oversight of Site Activation Specialist support resources.
What you will bring to the role
- Ability to be flexible
- An effective communicator, both written and spoken English, who demonstrates the ability to critically analyze and present information/data, communicate persuasively, and develop compelling visualizations (charts, graphics, etc.)
- Experience leading client discussions and escalations
- Ability to think creatively and solve problems
- Ability to process information and adapt to new information
- Ability to be patient with colleagues and peers
- Ability to work efficiently within a fast pace environment with short timelines with oversight
- Ability to function as part of and support/lead remote teams
- Excellent organizational skills
- Foundational knowledge of Site Identification
- Ability to travel for business needs (< 10%)
Your experience
- 5+ years of transferable experience in industry, health care, or data-driven feasibility
- Background in medicine, science, or other relevant discipline across a broad range of therapeutic areas, preferably with substantial international experience in clinical drug development
- Knowledge of the principles of Good Clinical Practice
- Minimum Bachelor’s degree or equivalent years experience
- Must have competent computer skills in MS Word, Excel, and PowerPoint
Requirements
- 5+ years of transferable experience in industry, health care, or data-driven feasibility
- Background in medicine, science, or other relevant discipline across a broad range of therapeutic areas, preferably with substantial international experience in clinical drug development
- Knowledge of the principles of Good Clinical Practice
- Minimum Bachelor’s degree or equivalent years experience
- Must have competent computer skills in MS Word, Excel, and PowerPoint
- An effective communicator, both written and spoken English, who demonstrates the ability to critically analyze and present information/data, communicate persuasively, and develop compelling visualizations (charts, graphics, etc.)
- Experience leading client discussions and escalations
- Ability to think creatively and solve problems
- Ability to process information and adapt to new information
- Ability to be patient with colleagues and peers
- Ability to work efficiently within a fast pace environment with short timelines with oversight
- Ability to function as part of and support/lead remote teams
- Excellent organizational skills
- Foundational knowledge of Site Identification
- Ability to travel for business needs (< 10%)
- Ability to be flexible
Benefits
- Competitive benefits package
Company overview
Worldwide Clinical Trials is a leading global contract research organization (CRO) that provides comprehensive clinical development services to pharmaceutical, biotechnology, and medical device companies. Founded with a mission to accelerate the development of innovative therapies, the company offers end-to-end solutions spanning from early-phase research through late-stage clinical trials and regulatory submissions. With expertise across multiple therapeutic areas including oncology, central nervous system disorders, cardiovascular diseases, and rare conditions, Worldwide Clinical Trials leverages its scientific knowledge and operational excellence to design and execute complex clinical studies. The organization maintains a global footprint with operations across North America, Europe, and Asia-Pacific regions, enabling it to conduct multinational trials efficiently. Known for its patient-centric approach and commitment to quality, Worldwide Clinical Trials plays a crucial role in advancing medical research and bringing new treatments to patients worldwide.