Who We Are
Es posible que un gran número de candidatos se presenten a este puesto, así que asegúrese de enviar su CV y su solicitud lo antes posible.
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands‑on, accessible leaders to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity, and we are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.
Business Development Operations Department Overview
Business Development Operations is a team of highly experienced professionals who drive significant booking targets and support Worldwide’s strategic position in a competitive market through a culture of collaboration and innovation. The team supports a strong portfolio of existing business and is responsible for the continued significant growth of Worldwide’s future pipeline and sponsors. They are accountable for overall sales performance, the profitable achievement of sales goals, and for aligning sales objectives with Worldwide’s therapeutic and commercial strategies.
What You Will Do
Identify operational needs for upcoming projects and track current assignments for CAT Operations staff
Resource CAT study projects as Resource Manager
Engage as a Subject Matter Expert for CAT Operations activities
Provide operational oversight for designated CAT study projects
Coordinate resourcing activities for all CAT awarded projects




Identify training and skills gaps among staff; coordinate and assist with learning opportunities
Actively identify and engage in process improvement activities
Participate in QMD reviews and new QMD development
Author, collaborate, and review QMD documents and guidance documents
Coordinate and manage CAT Operations team meetings
Oversee study risk assessments related to operational activities
Work with department leaders to ensure alignment among CAT operational and clinical services
Lead and/or contribute to departmental initiatives that implement policies, methods, techniques to grow service areas
Oversee CAT study deliverables from Launch to close out
Collaborate with Operations staff, Project Management, and Contracts on vendor and study budget development, scope revisions, tracking, and compliance
Assist in vendor management, including escalations, Vendor Management and Quality Assurance meetings
Review and assess ongoing budget utilization and revenue recognition to ensure projects meet financial targets
Manage internal CAT operations meetings and other trial‑specific meetings as appropriate
Contribute significantly to strategic departmental, sponsor‑related and cross‑functional initiatives
Participate in business development activities, including proposals input, capabilities and bid defense meetings
Apply thorough knowledge of industry regulations and guidelines to ensure operational compliance during clinical trial conduct
What You Will Bring To The Role
Exceptional organizational skills, detail‑oriented, and service‑oriented with excellent management and supervision skills
Excellent understanding of best business practices for clinical trial operations and rater reliability processes




Knowledge and capabilities of technology vendors and their abilities
Ability to plan, manage, monitor, and critique projects
Consistent meeting of timelines, ability to work under pressure
Openness to constructive, developmental feedback
Exceptional interpersonal skills in a fast‑paced, deadline‑oriented, changing environment
Proactive identification and escalation of potential project issues
Basic knowledge of statistics and finance practices
Your Experience
Minimum bachelor’s degree; Master’s degree (life sciences, MBA) and/or PMP certification preferred
Strong leadership, management and interpersonal skills
Strong planning and organizational skills
At least 7+ years clinical trial experience with at least 4 years’ experience in general clinical trials
Preferred ≥5 years of experience managing team members or project management experience
Hands‑on experience in day‑to‑day management of all aspects of global clinical trials
Prior experience in psychiatry / CNS therapeutic areas is a plus
Knowledge and appreciation of all stages of clinical drug development; proven ability to build high‑performance teams with strong monitoring practices and competence in CFRs, GCPs and ICH guidelines
Equal Opportunity Employer
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. xqbhyrx We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
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Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

📌 Associate Director, Operations - Clinical Assessment Technologies CAT) - UK/Europe - Remote (Valencia)
🏢 Worldwide Clinical Trials
📍 Valencia