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Clinical Research Specialist
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As a Clinical Trial Liaison, you will be the key to unlocking new opportunities for growth and development in the field of clinical research. Your ability to establish strong working relationships with investigators, study coordinators, and other stakeholders will play a crucial role in supporting the enrollment and conduct of our clinical studies.
Job DescriptionThe Clinical Trial Liaison is responsible for fostering scientific relationships with investigators and study coordinators to support enrollment while developing a deep understanding of clinical practice as it relates to areas of interest. This position interacts with various internal and external stakeholders, including institutions, their alliance partners (if applicable), study coordinators, pharmacists, clinical research associates, and investigators.
Key Responsibilities:- Establishes and maintains strong working relationships with Principal Investigators (PIs), Study Coordinators, and clinical trial sites to support the enrollment and conduct of our client's clinical studies.
- Works with our client and CRO Clinical Development and Clinical Operations leads and trial sites to understand and implement study protocols effectively.
- Follows up with sites post-SIV to ensure patient enrollment runs smoothly, identifies challenges, issues, and barriers, and reports back to our client and works with study teams and sites to develop solutions.
- Delivers medical/scientific education, as required, to trial sites and provides input to key internal stakeholders on training materials for clinical trials, therapeutic areas, and disease state as outlined by our client; suggests and supports implementation of local outreach options.
- Communicates investigator/study coordinator inquiries requiring follow-up to designated contacts and collaborates with clinical teams prior to providing approved responses to site inquiries appropriately to ensure focused and balanced clinical and scientific information.
- Bachelor's Degree in a scientific discipline.
- RN, BSN, MSN, NP, PA, PharmD, PhD, or MD with relevant clinical trial site experience.
- Cardiovascular experience is required; Oncology experience highly preferred. Experience working with injectable agents preferred.
- Knowledge of cardiovascular clinical trial/research design, conduct, and understanding clinical study results.
- Experience in clinical research, patient recruitment, or investigational site management.
- Strong oral and written communication skills; skilled at presenting scientific content.
Join a game-changing global company that is reinventing the way therapies are developed and commercialized. Here, each day brings an opportunity to take ownership of a new challenge. Teaming with some of the most talented clinicians in the industry, you'll improve patient outcomes and work in a dynamic environment to create better, smarter, faster ways to get biopharmaceutical therapies to patients.
Why Join Us?At Syneos Health, we're dedicated to accelerating innovation and improving patient outcomes. We believe that together, we can make a difference and create a healthier world. If you're passionate about clinical research and want to be part of a team that is shaping the future of healthcare, then we'd love to hear from you
