Clinical Trials Associate II

US-NC-Durham
Job ID
19058
# of Openings Remaining
1

About FHI 360

FHI 360 is a nonprofit human development organization dedicated to improving lives in lasting ways by advancing integrated, locally driven solutions. Our staff includes experts in health, education, nutrition, environment, economic development, civil society, gender, youth, research and technology — creating a unique mix of capabilities to address today's interrelated development challenges. FHI 360 serves more than 70 countries and all U.S. states and territories. We are currently seeking qualified candidates for the position of: Clinical Trials Associate

Description

Global Research Services (GRS) helps support and conduct clinical research in low-resource settings around the world. Our team includes clinical project managers, clinical research associates, research assistants, laboratory technologists, laboratory auditors, document specialists and instructional designers.

With culturally sensitive and multilingual employees in the United States, Africa, Asia, Latin America and Europe, GRS offers the following services to government and private sponsors:

  • Project management
  • Protection of participants’ safety and rights
  • Site identification, evaulation and development
  • Site monitoring, management and training
  • Research operations
  • Laboratory capacity building, auditing, and training
  • Logistical support

GRS seeks an experienced CTA to provide support to our Clinical Research Project Managers, interacting with other parts of the organization and clinical systems to contribute to the strong implementation of clinical research.

Job Summary / Responsibilities

The Clinical Trials Associate (CTA) assists both the project management and clinical operations teams in the implementation a clinical trial.

  • Responsible for the collection, review, tracking, maintenance and archiving of essential study documents in the Trial Master File, ensuring that project-specific administrative documents (e.g., contact lists, etc.) are maintained, and ensures sites are supplied with all required materials and supplies.
  • This position has frequent contact with internal and investigator site personnel.
  • CTA could be responsible for managing individual, large, or complex studies / programs.
  • The CTA assists the clinical research teams in ensuring the most effective and efficient conduct of clinical research studies by providing administration and project tracking support.
  • The CTA supports clinical teams by performing tasks related to study management from start up to study completion.
  • This position is a key role in supporting project team needs.
  • Utilizes technology effectively to support clinical development processes; develops mastery of relevant systems (e.g. study management tools) and identifies new innovative ideas and shares best practices.

Qualifications

• Bachelor's Degree or its International Equivalent - Education, Health, Behavioral, Life or Social Sciences, International Development, Human Development or Related Field.Preferred Education and/or Experience:

• Master’s degree or its international equivalent preferred.

• Related prior work experience in clinical trials required.

This job description summarizes the main duties of the job. It neither prescribes nor restricts the exact tasks that may be assigned to carry out these duties. This document should not be construed in any way to represent a contract of employment. Management reserves the right to review and revise this document at any time.

We offer competitive compensation and an outstanding benefit package. Please click here to visit FHI 360's Career Center for a list of all open positions.

FHI 360 is an equal opportunity and affirmative action employer. FHI 360 is an equal employment and affirmative action employer whereby we do not engage in practices that discriminate against any person employed or seeking employment based on race, color, religion, sex, sexual orientation, gender identity, national or ethnic origin, age, marital status, disability, veteran status, genetic information or any other status or characteristic protected under applicable law.

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