Ref #: 23152

Employment type: Permanent - Full-Time

Location: US-TX-Austin

Posted: 01-Nov-2021


DOCS is currently seeking a Site Engagement Manager for the Southern US. This role requires a bilingual (Spanish/English) site manager supporting sites in the US and Mexico. The Site Engagement Manager is a critical component in the execution of a clinical trial. Engagement of highly motivated clinical investigators will enable the sponsor to maximize efficient and timely delivery of the sponsors clinical trials. This is great opportunity for a CRA with experience supporting sites as they participate in research studies who is interested in moving into a clinical trial management role.


- Develop, communicate, and execute Site Engagement Strategy/Plan working closely with the Sponsors Clinical Team and key internal stake holders throughout the life cycle
- Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication channels to create awareness of the sponsor and its activities thereby increasing their desire to partner with the sponsor.
- Support the clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the trials
- Support assigned studies from a regional and cultural perspective & support study teams with quality related visits as needed.
- Communicate regularly with global Site Engagement Team and work collaboratively to share information, insights, and experiences with team and key internal stakeholders/customers.
- Ensure appropriate engagement and communication with internal stakeholders regarding SPS site visits and related activities.
- Attend key therapeutic trainings/meetings and/or industry trainings

- BA/BS Degree required
- Ability to speak Spanish
- Ability to travel in both domestic and internationally
- A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e.g. clinical project manager, study director/coordinator, clinical research associate, patient/site engagement companies)

DOCS is the FSP division of ICON Clinical Research. We provide global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry.

DOCS is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.