Senior Specialist, Trial Site Support

23 hours ago

Cambridge, Massachusetts, United States TriNetX Full time
Job Description:

We are seeking a highly skilled Senior Specialist, Trial Site Support & Operations to join our team at TriNetX. As a key member of our global healthcare network, you will play a critical role in supporting our US-based hospitals through our virtual staff-augmentation program.

Your primary responsibility will be to support the Clinical Research Center (CRC) or equivalent departments at 4 to 5 assigned hospitals on behalf of TriNetX. Your goal will be to maximize the participation of the hospital in studies and other projects initiated through TriNetX, making "your" hospital a top performer on the TriNetX network.

You will be responsible for managing the TriNetX CONNECT service within the assigned hospitals, including managing study opportunities, liaising internally with the hospital, TriNetX, and sponsors. You will also facilitate participation of your assigned hospitals in clinical studies sponsored by our pharma and CRO clients by timely assessing incoming study opportunities or requests for information (CONNECT) based on hospital capabilities, patient population, and research interests.

As a key point of contact for clinical projects, you will participate in recruitment and study participant selection using the TriNetX interface when appropriate. You will build a professional relationship with all relevant stakeholders and individuals in the hospital to achieve your goals.

You will also help shape the program from its conception, contributing to the design, refinement, and roll-out, guiding and connecting the dots for further stages of program implementation. You will bridge both sides, serving as the liaison between TriNetX and the hospitals you support.

Internally, you will be the subject matter expert on aspects of clinical trial site operations and over time, TriNetX Connect, supporting operational oversight/KPI surveillance alongside serving as a consulting resource for the global healthcare network & commercial teams.

Finally, as a de-facto member of the CRC/hospital team, you will provide feedback to TriNetX on how the hospital partnership can be further strengthened and how we can bring additional value to our partners.

Qualifications/Requirements:
  • A minimum of 5-7 years' relevant training and experience resulting from prior operational clinical research roles within healthcare or sponsor organizations.
  • Experience and oversight in pre-study evaluation, study initiation, treatment observation, or study close out.
  • Experience working with principal investigators within varied therapeutic areas and departments, aiding in strategy to integrate clinical research within hospitals.
  • Demonstrated knowledge and competency in GCP, understanding of site compliance with research protocols and regulatory requirements.
  • Knowledge of medical terminology, procedures, medications, coding, public health/healthcare, clinical research ecosystem.
  • Strong business acumen, oral and written communications skills, and the ability to successfully interface and build relationships at all levels in the organization.
  • Ability to work closely with, maintain accountability for, and influence related cross-functional groups and other internal and customer stakeholders.
Educational Expectations:

Professional healthcare qualifications/registration where applicable. Bachelor's degree or higher (graduate degree or advanced certifications preferred).

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