Clinical Project Manager-Permanent
Small Niche CRO- Office based Surrey
Introduction
Our client is a small niche CRO, focusing on early Phase drug development. If you're looking for a diverse and stimulating work environment with a broad remit, one where yourunique talents and skills can have a tremendous impact, you'll find it here, our client seeks to grow their business and implement the skills and experience of all staff. If you want to work in an environment where your ideas can be shared and implemented, if you want to work in a collaborative and supportive company, if you want to have a role with a broad remit where your entrepreneurial and resourceful contributions can really make an impact then this could be just the opportunity for you.
Job Summary
Our Client is expanding and is seeking resourceful solution focused Project Manager with early phase experience, passionate about delivering to a high standards. This role offers a rare opportunity to join a small but successful company in a key client facing role, with a remit that will cover preparing study bids, attending bid defence, study planning and full implementation through to report writing
Responsibilities
- You will be the project lead & main^point of contact for all assigned early Phase clinical studies
- Provide study updates to key stakeholders
- Ensure that all projects are delivered to the agreed scope of work and the highest standards
- Be the central point of contact for clients
- Liaise withand manage third party vendors as required including Phase I units
- You will have direct client contact & will work closely with them on project timelines
- Manage studies to both budget and timelines escalating any perceived deviation
- Develop and manage contingency plans as required
- With input from the client provide protocol review and protocol development
- Design and produce key study documents
- Attend and contribute to bid defence meetings
-Assist in the identification, selection and management of third party vendors and business partners
-You will work closely with internal colleagues and external vendors
- Develop new business opportunities from current clients and new clients
Required Education^
UniversityDegree (life science) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
Essential Skills
• Previous study management experiencewithin a CRO, Phase I unit or Pharma company
• Understand the financial aspects of running early phase studies
• Previous experience in Phase I/II studies would be advantageous
• Be client focused
• Happy to work to tight deadlines
• Enjoy communicating with internal staff/external sponsors at all levels
Our Clients Offers
Our client is an established company with a proven and respected track record built on a commitment to good science. Working with a broad range of multinational pharmaceutical and biotechnological companies as well as the medical research community. The atmosphere within the company is warm and congenial, with emphasis on open discussions, team spirit, mutual respect and trust. Encouraging independence and welcoming enthusiastic individual with a good sense of humour who enjoy working in a challenging and dynamic environment where good ideas can be shared and implemented and people can grow with the company.
Supplementary Requirements:
Software Competence: MS Office, MS Project
Valid Driving License: Essential
Working Language(s): English
Requirement for Business Travel: Yes
Flexible Working Hours: No
Employment Information:
Employer: CRO
Employment Type: Permanent
Hours:Full time
Location: Surrey
Plan Start Date: Negotiable
Benefits: 28 days holiday
Keywords:
MS Office, Medical Affairs, KOL, publications, IIS, Late Phase, lifecycle, Clinical Research, Clinical Operations, Clinical R&D,CRA, CTM, Project Management, GCP, Site Manager, observational, Manager, Study Manager, , ICH GCP, Project Manager, Clinical Study, Clinical Programme, Feasibility , Essential Documents, GCP, SOPs, Compliance, Training, Investigator Meeting, REC, Research Ethics. R&D,Trust, SMO, Site Manager, Quality Control, QC,EDC, Phase I, Early, proof of concept
Assigned Consultant Stewart Hulse at CSL Recruitment on 01932 219321
Please feel free to call for a detailed Job Description or additional information
Applicationsare reviewed within 24hrs, applicants will only receive feedback if they demonstrate the skills the role requires in their application. The role may be remarketed; if you applied for this role previously and were unsuccessful you will not^receive a response. We request that non EU Nationals include evidence of right to work in the country concerned with their application to be considered. Do supply supplementary information on required location, notice period and expected salary/day^