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Remote Clinical Trial Liaison, Hematology/Oncology (W. CA/APAC)

Company: The Medical Affairs Company (TMAC)
Location: Washington
Posted on: January 16, 2022

Job Description:

Territory will cover the US and APAC remotely (Australia, Taiwan, S. Korea, Singapore and Malaysia) region virtually. Must reside on the West Coast.

The Clinical Trial Liaison (CTL) will support the Company's Clinical Development program. The CTL will work full time to educate, analyze, and resolve issues with clinical research sites and investigators. Acting as a liaison between Company, the clinical study sites and the clinical trial manager (CTMs) the CTL will be responsible for conducting outreach to clinical investigators and site staff to implement and coordinate clinical trial recruitment efforts with the ultimate goal of achieving enrollment timelines. This position will include compliance, regulatory and study specific training.

Duties and Responsibilities:
Engage site staff and investigators in discussion to understand and report challenges in subject enrollment and retention and offer potential solutions via the development of site-specific recruitment plans.
Assist in the implementation and oversee the execution of site-based patient recruitment tactics
Communicate investigator/study coordinator inquiries requiring follow-up to designated contacts within Company and/or the Clinical Research team.
Interpret and report findings with recommendations for action to relevant stakeholder.
Work toward meeting established program metrics
Upon request, educate clinical trial sites and referring physicians about clinical trial protocol, disease state or study design.
As assigned, attend local, regional and national medical conferences, to obtain new competitive information, stay informed of clinical trends and support and maintain relationships with key investigators.
Complete all administrative responsibilities consistent with SOPs and departmental guidelines including but not limited to required training, field activity documentation, expense reporting, and other assigned tasks
Participate in and successfully complete all internal education/training on SOPs, policies, and relevant products, as well as all compliance training and regulatory education relevant to pharmaceutical industry
Interact and build positive relationships with key stakeholders on the Clinical Research team such as the site's assigned study team members including field monitors and CRAs.
Communicate any adverse event information, reports of concern or product complaints in accordance with Company's policies.

Qualifications:
Significant relevant clinical trial experience, a healthcare/science background and a BA/BS or equivalent are required.
5+ years of hands on experience with clinical trial recruitment and enrollment
Proven ability to manage multiple tasks under limited direction while generating quality deliverables
Demonstrated ability to prioritize and handle multiple tasks with changing deadlines
Requires low direct supervision
Team player with excellent people skills and strong customer focus
A working knowledge of compliance and regulatory requirements
Demonstrated ability to develop positive collaborative relationships
Excellent oral and written communication skills and interpersonal skills
Exceptional organizational and time management skills
Knowledge of FDA compliance and regulatory requirements
Ability to integrate and work in cross functional network
Ability to manage a geographically assigned territory from a home based office
Willingness to travel within the assigned region is required; overnight travel is required as needed
Demonstrated project management ability
Computer skills including Excel, Word, Power Point, Outlook and virtual meeting platforms are expected.
Valid driver's license

Keywords: The Medical Affairs Company (TMAC), Washington DC , Remote Clinical Trial Liaison, Hematology/Oncology (W. CA/APAC), Healthcare , Washington, DC

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