Operations Associate, Clinical Assessment

hace 4 meses

México Worldwide Clinical Trials A tiempo completo

**Requisition Number**7914**

**Employment Type**:Regular**

**Who we are**

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.

Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.

**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. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us

**What Clinical Assessment Technologies does at Worldwide**

The Operations Associate has primary responsibility for carrying out all daily aspects of the operational work related to rater selection, rater certification/qualification, rater training content, scale acquisition, surveillance maintenance, workbook/source document, for Worldwide Clinical Trials, Inc. (WCT). The Operations Associate is responsible for ensuring all assigned projects are conducted in a timely fashion and in a manner compliant with SOPs and ICH/GCP/regulatory guidelines. The Operations Associate works under the direction of the Operations Manager, Clinical Assessment Technologies (CAT).

**What you will do**

Tasks may include but are not limited to:

- Track the collection, entry, and distribution of rater experience qualification data
- Review and may develop study specific rater training web portal specifications for portal readiness
- Assist in coordinating logístical matters and prepare materials for Investigators’ Meetings, which Associate may attend
- Edit / format materials such as for rater training, including Excel spreadsheets, PowerPoint training slides, and Microsoft Word
- Conduct scale management activities, such as obtaining scale licenses, translations, regulatory authorizations, and Sponsor approvals
- Track incoming source documentation to ensure timeliness of source reviews and provide data to the Sponsor and study team
- Communicate with research sites to ensure rater training and data surveillance plan guidelines are followed
- Provide CAT data for the CAT Final Study Report completion and ensure proper formatting of document
- Other Clinical Assessment Responsibilities
- Assist Operations Manager to ensure budgetary demands are met per CAT project
- Conduct CAT study material archiving

Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

**What you will bring to the role**
- Highly organized, detail
- and service-oriented
- Meets timelines consistently and be able to effectively work under pressure
- Continuously open to constructive, developmental feedback
- Skilled in written and verbal communication in order to clearly and concisely present information
- High level of interpersonal skills in a fast-paced, deadline oriented, and changing environment
- Able to manage multiple tasks and many administrative details in a fast-paced and constantly changing environment
- High level of self-motivation skills
- High level ability to work in teams

**Your experience**
- Preferred minimum of Associates degree
- At least 1+ years clinical trial experience
- Demonstrable knowledge of operational aspects Phase I-IV clinical
- Ample knowledge of SOPs and ICH/GCP/regulatory guidelines
- Competency working with data and numbers
- Fluency in English (will be required to write, speak and understand English to conduct day-to-day business)
- The role requires travel domestically and internationally in order to attend key meetings. The global nature of the position may also require the incumbent to occasionally manage their time flexibly in order to be responsive to stakeholders in different time zones.

We love knowing that someone is going to have a better life because of the work we do.

LI-CS1 #LI-Remote

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