Principal Investigator (hypertension study) - USA - TransPerfect

Work Location: USA (Remote)

Engagement Model: Independent contractor

Expected start: as soon as possible

Expected project end: end of January 2025

Estimated total workload: 108 hours

DataForce by TransPerfect is currently looking for an experienced principal investigator with a medical degree to oversee the research process of our data collection study related to high blood pressure.

Role Summary

The principal investigator will manage the whole cycle of the IRB process, from submission to approval, for our on-site blood pressure data collection study.

Key Qualifications:

• Doctoral degree (eg., MD, PhD) in a field related to the study (eg., cardiology or internal medicine with a specialization in hypertension or cardiovascular disease)
• Proven research experience in managing the IRB submission and approval process for clinical studies.
• Previous involvement in research related to hypertension or cardiovascular disease is highly desirable.
• In-depth understanding of ethical and regulatory requirements governing clinical research.
• Excellent communication skills, with the ability to convey complex regulatory concepts to diverse audiences.
• Strong interpersonal skills and the ability to work effectively in a collaborative team environment.

Key Responsibilities:

• Manage the entire IRB submission process, ensuring timely and accurate completion of all required documentation.
• Collaborate with regulatory affairs specialists to address any queries or modifications requested by the IRB.
• Work closely with multidisciplinary teams to conceptualize and design research studies, ensuring alignment with ethical and regulatory guidelines.
• Stay abreast of relevant regulations and guidelines, ensuring the study's compliance throughout its lifecycle.
• Provide guidance to the research team on ethical conduct and regulatory adherence.
• Facilitate communication between the research team, regulatory authorities, and IRB members.
• Work collaboratively with external partners, ensuring a smooth regulatory process.
• Maintain accurate and organized records related to the IRB submission and approval process.
• Ensure that all study documentation is in accordance with regulatory standards.
• Provide support and guidance to on-site investigators and clinical staff regarding ethical and regulatory policies.
• Collaborate with the research team to address any regulatory challenges that may arise during the study.

In case you have any questions about this role contact us at: DataForce.Sourcing@transperfect.com

DataForce by TransPerfect is part of the TransPerfect family of companies, the world’s largest provider of language and technology solutions for global business, with offices in more than 100 cities worldwide.

We offer high-quality data for Human-Machine Interaction to some of the most prestigious technology companies in the world. Our department focuses on gathering, enriching and processing data for Machine Learning in different AI domains.

To learn more about DataForce please visit us at https://www.transperfect.com/dataforce

TransPerfect provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law. For more information on the TransPerfect Family of Companies, please visit our website at www.transperfect.com.