Clinical Project Specialist Remote
Job description
For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
The Clinical Project Specialist provides general administrative project management support for the assigned projects. This is a full time role and can be offered on a remote basis.
Essential Functions:
- Perform general administrative tasks to support project management activities related to the clinical trial execution, e.g., assist with the development and formatting of documents, review, and reconciliation of study-specific information, etc.
- Supports the day-to-day operations of clinical study execution in compliance with applicable SOPs, ICH/GCP guidelines and other regulatory requirements.
- Assist with document collection, dissemination, tracking and filling as per the organizational process ensuring compliance with SOPs and processes, and all applicable regulations.
- Assist with the development and distribution of site binders as requested.
- Track and prepare study-specific information utilizing databases, spreadsheets, and other tools as assigned. This may include but is not limited to clinical and non-clinical supplies and services such as tracking of appropriate subjects and site activity/metrics, performing quality check activities across different components of the clinical trial.
- Set-up and coordinate meetings, take and distribute meeting minutes.
- Proactively identify and escalate issues that arise relate to support functional deliverables.
- Work closely with study team members and study manger to fulfill assigned study execution tasks.
- Support study material development
- Participate in process improvement and quality-related initiatives associate with study execution and departmental deliverables.
Qualified candidates will have:
- Experience within a pharmaceutical/clinical research environment - ideally with experience as a Clinical Project Specialist
- Excellent communication and interpersonal skills as the CPS interacts with many people of varying levels of responsibility for clinical trial programs.
- Must be able to prioritize tasks, plan proactively, and accomplish goals using well-defined instructions and procedures with minimal supervision.
- Excellent computer skills with experience using Microsoft Office (Outlook, Word, Excel, and Power Point) applications to prepare charts, tables, forms, reports, and presentations required.
- Experience with email and calendar programs
- Electronic data capture (EDC), CTMS, IVRS, and eTMF experience is preferred.
- Relevant Bachelor’s degree is preferred.
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
Job Types: Full-time, Part-time
Part-time hours: 37.5 per week
Pay: Up to £55,000.00 per year
Benefits:
- Company pension
- Employee discount
- Private medical insurance
- Referral programme
- Sick pay
- Work from home
Schedule:
- Day shift
- Monday to Friday
Supplemental pay types:
- Bonus scheme
Work Location: Remote
Reference ID: 1362
