Principal Investigator

5 months ago

London, United Kingdom ProMed Innovations Ltd Full time

**About us**

We are professional, agile and inclusive.

Our work environment includes:

- Modern office setting
- Food provided
- Relaxed atmosphere
- Work-from-home days
- Modern office setting

Overview:
We are seeking a highly qualified and experienced individual to join our team as a Principal. As the Principal, you will be responsible for providing leadership and guidance to our educational institution. This is a key leadership role that requires strong communication skills, effective decision-making, and the ability to foster a positive learning environment.

**Duties**:

- 1. Serve as the primary point of contact and oversee all aspects of industry-sponsored clinical trials in neurology and Alzheimer's disease, from study initiation to closeout.
2. Provide leadership and guidance to the clinical research team, including study coordinators, nurses, and other staff members, to ensure compliance with study protocols, regulatory requirements, and ethical standards.
3. Collaborate with sponsors, contract research organizations (CROs), and other stakeholders to develop and implement study protocols, informed consent forms, and other study-related documents.
4. Ensure that study procedures are conducted according to Good Clinical Practice (GCP) guidelines and applicable regulations.
5. Oversee the screening, enrollment, and follow-up of study participants, ensuring their safety and well-being throughout the duration of the trial.
6. Collect, review, and analyze study data to ensure accuracy, completeness, and compliance with study objectives and regulatory requirements.
7. Prepare and submit study progress reports, safety updates, and other regulatory documents to regulatory authorities and ethics committees as required.
8. Participate in investigator meetings, site initiation visits, and other study-related activities as necessary.
9. Stay informed about the latest developments and advancements in neurology and Alzheimer's research, attending conferences, workshops, and continuing education programs as appropriate.
10. Foster a culture of excellence, collaboration, and continuous improvement within the clinical research team, promoting a positive and supportive work environment.

Qualification:

- Proven track record of successful study conduct, including protocol development, patient recruitment, and data management.
- Strong knowledge of GCP guidelines, ICH regulations, and FDA requirements related to clinical research.
- Excellent communication, leadership, and interpersonal skills, with the ability to collaborate effectively with sponsors, investigators, study staff, and other stakeholders.
- Detail-oriented and able to multitask effectively in a fast-paced environment.

**Job Types**: Part-time, Temporary contract, Freelance, Zero hours contract
Contract length: 12 months

**Salary**: £55,870.00-£67,597.00 per year

Expected hours: 4 - 16 per week

**Benefits**:

- Free parking
- Work from home

Schedule:

- Flexitime

Supplemental pay types:

- Bonus scheme
- Commission pay
- Performance bonus
- Tips
- Yearly bonus

**Experience**:

- Statement Taking: 1 year (preferred)
- Investigations: 1 year (preferred)

Licence/Certification:

- Driving (preferred)

Work Location: Hybrid remote in London

Reference ID: PMI/243/021

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