What are the responsibilities and job description for the Study Start Up Coordinator position at DelRicht Research?
Why DelRicht?
Would you love to be a part of the cutting edge of healthcare and science innovation? Do you enjoy managing projects and making sure everyone on the team has the information they need to be successful? Are you looking for a position that has opportunities for professional growth? If the answer is yes, then DelRicht Research might be the right opportunity for you!
Who We Are
DelRicht is a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new treatment options for our patients and ultimately our goal is to get new medications and medical devices FDA approved! We hold our team members to a high standard of excellence and are looking for energetic, positive, quick learners to be a part of our team. Presently our network stretches across 33 sites in 18 states.
Position Main Objective: As a DelRicht Study Start Up Coordinator you will play a key role in planning, executing, and overseeing clinical research projects to ensure successful completion while adhering to regulatory guidelines and ethical standards. This is a project management role which requires top-notch communication. We’re looking for a go-getter! You will work closely with multiple departments, investigators, and sponsors to ensure successful execution of clinical research protocols.
NOTE: This is a full-time onsite position in New Orleans, LA. No hybrid or remote-seeking candidates, please. Preference will be given to local applicants.
Job Description
The Study Start Up Coordinator will maintain all activities related to the conduct of clinical trials including but not limited to:
Production
Visit our website linked below to learn about our company and current clinical trials, see patient testimonials, and check out our careers page!
Website: www.delrichtresearch.com
Patient Testimonials: https://delrichtresearch.com/testimonials/
We are an equal opportunity employer and consider all qualified applicants equally without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.
Would you love to be a part of the cutting edge of healthcare and science innovation? Do you enjoy managing projects and making sure everyone on the team has the information they need to be successful? Are you looking for a position that has opportunities for professional growth? If the answer is yes, then DelRicht Research might be the right opportunity for you!
Who We Are
DelRicht is a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new treatment options for our patients and ultimately our goal is to get new medications and medical devices FDA approved! We hold our team members to a high standard of excellence and are looking for energetic, positive, quick learners to be a part of our team. Presently our network stretches across 33 sites in 18 states.
Position Main Objective: As a DelRicht Study Start Up Coordinator you will play a key role in planning, executing, and overseeing clinical research projects to ensure successful completion while adhering to regulatory guidelines and ethical standards. This is a project management role which requires top-notch communication. We’re looking for a go-getter! You will work closely with multiple departments, investigators, and sponsors to ensure successful execution of clinical research protocols.
NOTE: This is a full-time onsite position in New Orleans, LA. No hybrid or remote-seeking candidates, please. Preference will be given to local applicants.
Job Description
The Study Start Up Coordinator will maintain all activities related to the conduct of clinical trials including but not limited to:
- Lead and manage clinical research projects from initiation to completion, ensuring adherence to timelines and quality standards.
- Identify project risks and develop strategies to ensure successful project execution.
- Monitor study progress and proactively identify any deviations, resolving issues promptly to prevent delays.
- Lead and motivate clinical teams to achieve project objectives and milestones.
- Facilitate effective communication between team members, clients, and vendors.
- Ensure all clinical research activities are conducted in compliance with relevant regulations, Good Clinical Practice (GCP), and company SOPs.
- Perform quality checks to ensure data accuracy and integrity, and resolve any discrepancies promptly.
- Oversee data collection, analysis, and reporting activities in coordination with the data management team.
- Prepare project progress reports, ensuring clear communication of study status and key performance indicators to stakeholders.
- Be self motivated! Energetic! Positive!
- Focus on providing exceptional patient care and creating memorable experiences
- Make sure client satisfaction is a primary focus and that the client is able to achieve and exceed their goals
- Believe in high quality and have a high standard of compliance to our study protocols
- Be remarkably organized
- Be skilled at problem solving
- Manage multiple tasks and clinical trials efficiently
- Accept ownership of tasks from inception through completion and assume responsibility for personal success
- Required: 1-2 years of professional work experience
- Required: B.S or B.A from any accredited university
- Required: Proficient in utilizing technology, including relevant software applications and tools required for the role
- Preferred: Proven skill in constructing and analyzing spreadsheets
- Preferred: Experience working cross-functionally across departments/shared services teams, etc.
- Coffee drinkers preferred. Tea drinkers accepted.
Production
- We deliver on our promises
- We have a bias towards action: we value independent problem solving
- We proactively over deliver: we can act without being told what to do and we always have new ideas that will be heard and will improve the company
- We support each other relentlessly
- We always have enthusiasm: we exhibit passion and excitement about our work which leads to everyone having a ‘can do’ attitude
- We embrace change: we are excited to always be growing and moving the organization forward which means change is the norm for us
- Coachable: we all love to learn, we are willing to be taught and will adapt quickly
- We always are able to execute: we get it right the first time and promote ‘touch it once’ accuracy
- We have persistence: we demonstrate the tenacity and willingness to go the distance to get something done
- We are calm under pressure: we can maintain stable performance when under heavy pressure or stress
- Medical, Dental and Vision Insurance
- Short Term Disability, Long Term Disability, and Life Insurance
- Generous Paid Time Off that builds throughout your career with the company
- Even though we are in healthcare, we do not work nights, weekends or 12 hour shifts (yes, nurses love us!)
- 401K (includes discretionary match/profit sharing)
- Exceptional quarterly bonus plan that clearly outlines your bonus potential per quarter
Visit our website linked below to learn about our company and current clinical trials, see patient testimonials, and check out our careers page!
Website: www.delrichtresearch.com
Patient Testimonials: https://delrichtresearch.com/testimonials/
We are an equal opportunity employer and consider all qualified applicants equally without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.