Clinical Research Study Coordinator

Come join our growing team PCR is expanding the Clinical Research department at our site in Chelmsford Essex UK. We conduct studies for local, national, and international companies, testing cosmetics, personal care products, food, fragrance and clinical projects for many large companies.

Due to our growth, we have a need for **Clinical Research Study Coordinator's and Clinical research Assistants** within our Research facility Here is your opportunity to be a part of one of the biggest consumer product testing companies in the world
- _**This is a full time position.**_ **Summary**: The Research Study Coordinator oversees and coordinates the daily activity of clinical research studies. They work closely with the clinical teams and investigators to ensure that all protocol required procedures and visits occur according to protocol specific guidelines. **Essential Functions**: The ability to work both independently and within a team to ensure the study is performed as described in the research protocol.
- The ability to quickly learn and perform technical tasks associated with a study and perform them with a high degree of accuracy and focus.
- The ability to communicate and interact with clients, panelists and team members in a professional, collaborative manner.
- A high level of flexibility/availability including early morning, afternoons, occasional evening and weekend shifts as needed.
- The ability to stand, sit, bend and engage for extended periods of time.
- The ability to perform quality results in a fast-paced, high energy work environment.

**You Will**:

- Be responsible for organizing all aspects of the clinical trials assigned.
- Participate in investigator meetings, site initiation meetings, etc. as needed.
- Work with our internal recruitment department for participant enrollment and ensure compliance with protocol and all applicable regulations.
- Conduct informed consent process.
- Conduct study related visits.
- Assess, monitor and report adverse events per protocol.
- Maintain required records of study activity including source documentation, case report forms, drug dispensation records, and data management system entry.
- Dispenses test articles, calculate dosages if needed and provides instruction.
- Complete case report forms and resolve queries.
- Report protocol deviations to PI, sponsor and IRB as required.
- Obtain, process and ship study related specimens.
- Provide assistance to fellow study coordinators.
- Manages quality assurance activities for assigned protocols per site SOP’s.
- Submits regulatory documents to IRB and Sponsor, including initial site submission, continuing review, final report, reportable protocol deviations, and reportable SAE’s.
- Prepare study for initiation.
- Ensures and documents protocol amendment training for all study staff, as needed.
- All other related duties as assigned.

**Education**:

- Associate’s Degree
- NO minimum experience is required, just the willingness to learn However, if you do have some experience, we would love to hear from you and see how we can encourage you to join our team

**Knowledge, Skills and Abilities**:

- Demonstrated leadership experience. Must be able to demonstrate leadership by serving as an example to others with regard to professional behavior, handling multiple tasks, maintaining a positive attitude, and in response to organizational change.
- Proficiency with Microsoft Word, Excel and PowerPoint.
- Must possess excellent leadership, organizational, computer, and communication skills.
- Ability to work effectively and cooperatively with staff, board, clients, and the public.
- Ability to multi-task, prioritize appropriately, and work well both individually and as part of a team.
- Ability to use time productively and contribute to high levels of company operational efficiency and effectiveness.
- Ability to maintain confidentiality of information.

**Physical Demands**:

- Ability to communicate in an active multi-office environment.
- Ability to efficiently operate all job related office equipment (telephone, computer, calculator, fax, copier).
- Ability to communicate via telephone.
- Ability to sit for large portions of a workday.

**Here are just a few things we offer**:

- Great pay and benefits
- Access to health insurance
- Access to voluntary short term disability insurance and additional life insurance
- Very attractive retirement package
- Generous holiday schedule

**Salary**: £45,000.00-£60,000.00 per year

**Benefits**:

- Relocation assistance

Schedule:

- 10 hour shift
- 8 hour shift

Work Location: In person