Worldwide Clinical Trials

Medical Director (Investigator)

SAN ANTONIO, TXPosted a month ago

Job summary

  • Job post source

    This job is directly from Worldwide Clinical Trials

  • Job overview

    The Medical Director (Investigator) role at Worldwide Clinical Trials involves overseeing clinical investigations to ensure protocol adherence, patient safety, and data integrity, contributing to the company's mission to improve lives through innovative clinical research.

  • Responsibilities and impact

    The Medical Director ensures protocol compliance, manages patient care, protects subject rights, validates data, documents study procedures, oversees investigational agent use, and supports site operations and clinical staff supervision.

  • Experience and skills

    Candidates must have a Medical (M.D.) degree with at least 2 years of clinical research experience, strong supervisory, communication, organizational, and conflict resolution skills; preferred experience includes 5 years in clinical research with 2 years in Phase 1 studies.

  • Work environment and culture

    Worldwide Clinical Trials fosters a diverse, inclusive, and collaborative environment with accessible leadership and supportive teams, encouraging professionals to thrive and do their best work.

  • Company information

    Worldwide Clinical Trials is a global midsize CRO with over 3,500 experts focused on pioneering and innovative clinical research to find cures for persistent diseases.

Company overview

Worldwide Clinical Trials is a global contract research organization (CRO) that provides phase I-IV clinical trial services to the pharmaceutical and biotechnology industries. They specialize in therapeutic areas such as neuroscience, cardiovascular, metabolic, and rare diseases. Founded in 1986, the company has grown to operate in more than 60 countries, leveraging their scientific expertise and innovative technologies to deliver high-quality data and support drug development. Their revenue is primarily generated through service contracts with pharmaceutical companies, offering comprehensive clinical trial management, data analysis, and regulatory support.

How to land this job

  • Position your resume to highlight your Medical (M.D.) degree and emphasize your clinical research experience, especially your time as an investigator or sub-investigator, to align with the Medical Director role at Worldwide Clinical Trials.

  • Focus on showcasing your expertise in protocol compliance, patient care, Good Clinical Practices, and your ability to supervise clinical staff, as these are key responsibilities in the job description.

  • Apply through multiple platforms such as Worldwide Clinical Trials' official careers page, their corporate website, and LinkedIn to maximize your chances of being noticed for this position.

  • Connect with current Medical Directors or clinical research leaders at Worldwide Clinical Trials on LinkedIn. Use ice breakers like commenting on their recent publications, expressing admiration for the company's pioneering approach, or asking about the team culture to start a conversation.

  • Optimize your resume for ATS by including keywords such as 'protocol compliance,' 'clinical research,' 'Good Clinical Practices,' 'patient care,' 'investigator,' and 'clinical supervision' to help your resume pass initial screenings.

  • Use Jennie Johnson's Power Apply feature to automate applying through multiple channels, tailor your resume with the right keywords, and identify relevant LinkedIn contacts for networking, allowing you to focus your energy on preparing for interviews and follow-ups.

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