Principal Investigator - London, United Kingdom - ProMed Innovations Ltd

Description

About us
We are professional, agile and inclusive.


Our work environment includes:

• Modern office setting
• Food provided
• Relaxed atmosphere
• Workfromhome 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 industrysponsored clinical trials in neurology and Alzheimer's disease, from study initiation to closeout.
• 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.
• Collaborate with sponsors, contract research organizations (CROs), and other stakeholders to develop and implement study protocols, informed consent forms, and other study-related documents.
• Ensure that study procedures are conducted according to Good Clinical Practice (GCP) guidelines and applicable regulations.
• Oversee the screening, enrollment, and follow-up of study participants, ensuring their safety and well-being throughout the duration of the trial.
• Collect, review, and analyze study data to ensure accuracy, completeness, and compliance with study objectives and regulatory requirements.
• Prepare and submit study progress reports, safety updates, and other regulatory documents to regulatory authorities and ethics committees as required.
• Participate in investigator meetings, site initiation visits, and other study-related activities as necessary.
• Stay informed about the latest developments and advancements in neurology and Alzheimer's research, attending conferences, workshops, and continuing education programs as appropriate.
• 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.
• Detailoriented and able to multitask effectively in a fastpaced 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:
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