Director, Clinical Site

We are now recruiting for a Clinical Research Site Director responsible for the overall coordination, organization, and efficient implementation of clinical trials marketing, operations, and regulatory compliance. Works closely with the Principal Investigator to evaluate clinical trials and ensure that all study-related procedures are correctly completed from a clinical and a regulatory perspective.

Velocity Clinical Research’s integrated approach requires provides excellent care for patients and high-quality data to sponsors. The role of our Clinical Research Site Director is paramount to achieving our objectives; as a Clinical Research Siter Director, you may be responsible for the following tasks:

• Support the identification of strategies to expand the research capabilities at the site in line with the overall site business plan.
• Lead the implementation and maintenance of quality standards at the site, ensuring the conduct of clinical studies and the collection of patient data is in accordance with ICH GCPs.
• Develop site staffing plans to ensure the successful conduct of research studies.
• Lead the development of the patient recruitment plans and patient outreach process for studies.
• Manage the performance of site staff members, including staff conduct and performance.
• Identify and build relationships with outside medical practices, pharmacies, and other health care professionals/organizations to aid in the patient recruitment process.
• Support business development activities on behalf of the site and with sponsors, CROs, CRAs, and any third-party study vendors, as appropriate.
• Share best practices with other locations to raise the overall level of operational competencies.
• Support the completeness, accuracy, and timeliness of Feasibility Questionnaires, CDAs, CVs, and essential regulatory documents from study start-up phase until site initiation.

Successful applicants will have the following:

• Bachelor’s degree required and 7 years of clinical research drug trial management experience at the clinical investigator site level, or a combination of equivalent training and relevant industry experience.
• Expertise in project management, knowledge of field organizational strategies, extensive knowledge of clinical research, strong communication and presentation skills.
• High level of attention to detail.
• Personable, able to build rapport with staff, patients, and sponsors with ease.
• Motivated about a career in clinical research

What’s Next?

• Confirmation of your application – if you don’t see it, check your junk mail folder.
• A key part of the review process is to evaluate your Candidate Profile with job requirements; therefore, please make sure your profile is accurate and extensive to give you the best opportunity for us to get to know you!
• Watch for an email or text from us to keep up with your application status.

Eligible Employees are offered a comprehensive selection of benefits they may choose to elect, including:

• 
  Multiple Velocity subsidized Medical, Dental, and Vision Plans
• FSA and HSA with employer matching accounts
• Velocity matching 401k plan
• Velocity Paid Short and Long Term Disability, Basic Life and AD&D
• Accident Insurance • Critical Illness • Voluntary Employee, Spouse and Child Life and AD&D

To be considered, you must theVelocityClinical.com

Monday - Friday | Weekends upon request | Some roles may offer overnight opportunities | 100% on site, no remote work available

We do not accept unsolicited resumes from recruiting agencies.