Job Title: Principal Investigator

Job Description

We are seeking a dedicated and meticulous Principal Investigator to lead and conduct clinical trials, ensuring adherence to ICH/GCP and local regulations. The role involves working closely with study protocols, recruiting eligible participants, and overseeing their clinical evaluations and investigations. This position offers the opportunity to make a significant impact in clinical research without prior experience, as comprehensive training will be provided.

ResponsibilitiesAct as a Principal Investigator or Sub-Investigator ensuring ICH/GCP and local regulations are met at all times.Conduct clinical trials in line with the protocol and ensure the recruitment of eligible participants onto the study.Follow study protocols and Standard Operating Procedures (SOPs).Perform study-specific tasks as per the study-specific delegation logs.Provide information and support to consenting participants for a clinical study.Carry out clinical evaluation and clinical investigation of participants.Ensure serious adverse events/adverse events are reported appropriately.Take responsibility under PI guidance for the medical wellbeing of participants during the clinical trial and referral to specialists or GP as required.Act courteously and politely when dealing with patients, responding to any concerns or complaints in accordance with company SOPs.Ensure all study documentation is completed, signed off, and actions are taken as appropriate.Exercise meticulous attention to detail in recording patient information and data ensuring any queries are acted upon in a timely and efficient manner.Constantly seek and suggest quality improvements.May participate in CST (but not as a Lead Medic).Deputize for other PIs when needed as authorized by the PI (during absence, holidays, etc.) and in line with SOPs.Participate in the Out of hours on-call rota under the guidance and direction of the medic at the site.Participate in weekly PI meetings, site clinical meetings, and other company meetings as required.Liaise with and develop positive relations with sponsors, clients, and monitors as required.Ensure competency assessments are performed as per SOPs.Take ownership of being prepared for all GMC appraisals/Revalidation.Participate actively in the performance review process.Complete regularly weekly timesheets as required.Attend and log regular 1-1 meetings with People Leader and direct reports as required.Complete all study-specific and non-study-specific training on time.Work under pressure to a very high standard and meet all deadlines.Provide information to Medical Director, Site Business Manager, and other managers when requested in a timely manner.Reply to any communication from seniors, other members of staff, clients, and patients in a timely manner as per the standards of communication.Project a helpful and courteous company image and maintain a professional attitude and appearance.Perform any commercial tasks requested by the Medical Director.Essential SkillsCertified Neurologist2-6 years of experience as a licensed NeurologistAdditional Skills & QualificationsQuality controlQuality assuranceNeurologyWork Environment

This position is on-site, either in Wilmington, NC or Charleston, SC, where you will oversee day-to-day operations and provide quality assurance for all trial documents being submitted. The work environment is professional and requires maintaining high standards under pressure.

Pay and Benefits

The pay range for this position is $100.00 - $140.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Charleston,SC.

Application Deadline

This position is anticipated to close on Feb 27, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.