Job
Description
As an employee of Velocity Clinical Research, you play a crucial role in the organization's mission to bring innovative medical treatments to patients. Your dedication and performance are valued, and Velocity is committed to supporting your career growth and rewarding your achievements. Whether you are new to clinical research or an experienced industry professional, Velocity invites you to be a part of their team. Benefits offered by Velocity include medical, dental, and vision insurance, paid time off, company holidays, a 401(k) retirement plan with company-match, and an annual incentive program. **Role Overview:** You will be responsible for preparing and maintaining complete and accurate source material to support the setup and delivery of clinical research studies at Velocity Clinical Research. **Key Responsibilities:** - Supports the initial review, creation, and set up of study documentation for timely study delivery with a focus on expedited study start-up. - Ensures timely setup of source documents to avoid delays in study start-up. - Follows a multi-step procedure to ensure data source integrity. - Communicates with site-level staff regarding amendments and changes to the source. - Adheres to safety and compliance regulations. - Assists new hires in completing and submitting all required research documentation and training by their deadlines. - Performs other duties as assigned. **Qualifications:** - **Required Skills/Abilities:** - Demonstrated knowledge of medical terminology. - Proficiency in using technology such as computers, Microsoft Office software, fax, copier, and multi-line telephone. - Strong verbal, written, and organizational skills. - Excellent interpersonal and communication skills. - Ability to work effectively as a team player. - Proficiency in English language. - Strong ability to multi-task and follow written guidelines. - Ability to work independently, plan, and prioritize tasks with some guidance. - Detail-oriented with a professional demeanor. - Understanding of ICH, GCP, and FDA regulatory requirements. - **Education and Experience:** - Bachelor's degree with 1 year of relevant experience in the life science industry OR - Associate degree with 2 years of relevant experience in the life science industry OR - High School Graduate and/or technical degree with a minimum of 3 years relevant experience in the life science industry **Physical Requirements:** - Prolonged periods of sitting at a desk and working on a computer. - Communication in person and by telephone. - Limited walking required. - Ability to lift up to 30 pounds at times. Velocity Clinical Research values your contribution and is dedicated to providing a supportive and rewarding work environment. Join the team to be part of an organization committed to making a difference in medical research and patient care. As an employee of Velocity Clinical Research, you play a crucial role in the organization's mission to bring innovative medical treatments to patients. Your dedication and performance are valued, and Velocity is committed to supporting your career growth and rewarding your achievements. Whether you are new to clinical research or an experienced industry professional, Velocity invites you to be a part of their team. Benefits offered by Velocity include medical, dental, and vision insurance, paid time off, company holidays, a 401(k) retirement plan with company-match, and an annual incentive program. **Role Overview:** You will be responsible for preparing and maintaining complete and accurate source material to support the setup and delivery of clinical research studies at Velocity Clinical Research. **Key Responsibilities:** - Supports the initial review, creation, and set up of study documentation for timely study delivery with a focus on expedited study start-up. - Ensures timely setup of source documents to avoid delays in study start-up. - Follows a multi-step procedure to ensure data source integrity. - Communicates with site-level staff regarding amendments and changes to the source. - Adheres to safety and compliance regulations. - Assists new hires in completing and submitting all required research documentation and training by their deadlines. - Performs other duties as assigned. **Qualifications:** - **Required Skills/Abilities:** - Demonstrated knowledge of medical terminology. - Proficiency in using technology such as computers, Microsoft Office software, fax, copier, and multi-line telephone. - Strong verbal, written, and organizational skills. - Excellent interpersonal and communication skills. - Ability to work effectively as a team player. - Proficiency in English language. - Strong ability to multi-task and follow written guidelines. - Ability to work independently, plan, and prioritize tasks with some guidance. - Detail-oriented with a professional demeanor. - Understanding of ICH, GCP, and FDA regulatory requirements. - **Education a
