Clinical Trial Specialist

Primary Talent Partners has a 2 year contract opening for a clinical trial associate to join a multinational pharmaceutical company for a fully remote position operating on East Coast hours. 

Pay: $33.00/hr - $38.00/hr
Contract: 2 years, conversion possible
Type: W-2, cannot support C2C or provide visa sponsorship
Remote: 100% remote - east coast candidates and central standard time candidates only.

Summary:
Under the direction of the Director, Study Management, the Clinical Trial Associate (CTA) Study Management, will be responsible for supporting the Global Clinical Trial Operations department, Study Directors and Study Managers in the conduct and oversight of the execution of Phase 2 - 3 studies, as well as post-approval and life-cycle management studies primarily focused in Women’s Health. This individual will play an important role with assisting Operational teams in executing and tracking deliverables that support the oversight of our clinical trials and Service Providers/vendors to ensure the integrity of our trials. The project tasks/activities handled by the CTA will support Directors and/or Associate Directors ensuring the consistency of operational aspects of the program/studies. As needed may liaises with internal/external partners, vendors, and vendor management. Will also support the department as needed with specific activities/assignments.

Responsibilities:

• Responsible for supporting the Study Management teams, conduct and oversight of our trials
• May interact with the Service Provider/vendors as needed to complete assigned trial support activities to ensure the conduct of clinical trials in line with program objectives are being carried out efficiently
• May be supporting multiple clinical trials
• Will support in the maintenance of study documents and eTMF reconciliation
• Responsible for assisting with the conduct of study team meetings including generation of agenda and minutes
• Responsible for assisting in the review and tracking of various study documents and study plans (such as Site Feasibility Questions, Site Selection Questions, Monitoring Plan, and any other relevant study plans)
• Generation of enrollment and study level metrics reports as needed
• Other duties as assigned to support the business needs of the organization
• May contribute to cross-functional/functional operational excellence initiatives.

Required Qualifications:

• Bachelor’s degree in Life Sciences with minimum 3 years of experience or MS in Life Sciences with minimum 1 year of relevant experience in clinical drug development.
• Practical experience working with of Service Providers/vendors for trial conduct
• Good level navigation skills in difficult situations
• Pharmaceutical and/or clinical drug development experience.
• Good organizational skills and ability to manage multiple tasks with meticulous attention to detail.
• Strong time management skills.
• Strong written and verbal communication, excellent knowledge of computer/database management systems.
• Meticulous attention to detail.
• Ability to listen effectively and the capability to effectively communicate ideas and data both verbally and in writing in an appropriate manner.
• Developing to strong project management skills.
•  Strong Powerpoint, SharePoint, Excel, Word, Outlook and online meeting tool skills.

Primary Talent Partners is an Equal Opportunity / Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws.

If you are a person with a disability needing assistance with the application or at any point in the hiring process, please contact us at info@primarytalentpartners.com

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