Job Description
Clinical Research Scientist -
Your Talent. Our Vision. At Princeton Consumer Research, Inc., one of the worlds biggest, independently- owned clinical research companies, it's a powerful combination. It's the foundation upon which we're creating greater access to research services for our clients, along with quality research services to back up our clients claims. Our focus is on quality, precise, accurate, data generation.
This is an exciting and rare opportunity to join our expanding team of Clinical Scientist’s based at our essex UK office. The Clinical Scientist will work with the Lead Clinical Scientist and provide scientific, clinical, and operational review and input for all clinical trials with an emphasis on protocol-specific, in-life clinical data monitoring activities.
You will;
- Work with cross-functional team with oversight by the Lead Clinical Scientist/Technical Director to conduct clinical studies, including clinical and safety data review, site interface on clinical study content preparation of meeting materials, communication plans (e.g., administrative letters, protocol amendments, protocol deviations), safety and hosting Client monitoring meetings, preparation of status update reports, and study close-out activities.
- Support other team members with monitoring reports, safety reviews, site interactions, and reviewing TFLs. Responsible for analytical support of clinical trial data (safety and efficacy), including gathering, analyzing, reviewing, interpreting, and providing preliminary assessments and recommendations to Clinical Lead/Technical Director. Analyze and synthesize information to assess issues relating to protocol conduct and/or individual subject safety.
- Provide clinical operational support for Data Monitoring, preparing updates and blinded data reviews, execution of meetings and adjudications if needed.
- Contribute to ICFs, training documents, literiture reviews and other clinical and regulatory documents under the direction of the Lead Clinical Scientist., including protocol development and study report generation
- Interact with internal and external stakeholders (study sites, vendors, IRB committees, etc.) in support of clinical trial objectives; responds to or triages questions for appropriate escalations. Client meetings and some travel maybe required.
- Contribute to the organization, preparation, and execution of investigator and advisory board meetings in collaboration with the project team and external vendors.
We're looking for someone who has;
- Life sciences degree coupled with clinical or pre-clinical research experience
- Experience in analysis and interpretation of clinical data (safety and efficacy); working knowledge of biostatistics, GCP, and regulatory requirements for clinical studies.
- Experience working with clinical trial sites.
- Excellent oral and written communication skills and solid computer/analytical skills.
- Ability to work collaboratively in a fast-paced, team-based matrix environment and to function independently as appropriate. With the ability to lead on a daily basis.
- Ability to handle multiple projects at a time and have a strong attention to detail while understanding the higher-level strategy. Able to prioritize the projects in terms of deliverables and making sure the project team understands your expectations as the project lead.
You will lead and support the scientific study design and development of client proposals, protocols, statistical analysis plans, reports, presentations, and publications, focusing on the interpretation of results and translation of results back to stakeholders.
You must lead and support the scientific, methodologic, and clinical development and direction of the research teams, including new product and services development and support, whilst promoting the company's research expertise in client meetings. Provide scientific mentorship to members of the research teams.
Qualifications
Requires an BSc, MS, PhD, PharmD, or equivalent advanced degree and 3+ years of experience in Clinical research, pharmacoepidemiology, biostatistics, consumer product testing, or related field
Strong research background that includes study design and analytical skills, ideally with knowledge of pre-approval and/or post-approval research. Record of publication in peer-reviewed scientific journals would be highly sought as this is an area that the company wants to invest.
Must have excellent oral, written, and presentation skills and have the ability to thrive in a constantly changing environment.
PCR is an equal opportunities employer and encourages applications from all sections of our community. Relocation package available for the right person.
Job Type: Full-time
Salary: £50,000.00-£80,000.00 per year
Schedule:
- 8 hour shift
- Monday to Friday
Ability to commute/relocate:
- Chelmsford: reliably commute or plan to relocate before starting work (required)
Education:
Experience:
- Science & Research Occupations: 1 year (required)
Job Types: Full-time, Permanent
Salary: £50,000.00-£80,000.00 per year
Benefits:
- Company pension
- Free parking
- On-site parking
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Ability to commute/relocate:
- Chelmsford: reliably commute or plan to relocate before starting work (required)
Work Location: One location
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