Senior Project Manager, UK
- Employer
- Simbec-Orion
- Location
- Homeworking, United Kingdom
- Salary
- Competitive
- Start date
- 19 Oct 2021
- Closing date
- 24 Oct 2021
View more
- Discipline
- Clinical Research, Clinical Project Manager
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Management
You need to sign in or create an account to save a job.
Job Details
Simbec-Orion is a responsive and agile full-service CRO, with wide therapeutic experience and specialist expertise in clinical pharmacology, oncology and rare diseases. Perfectly structured, we provide full-service clinical development solutions for small and mid-size drug developers - headed up by a centralised leadership team.
With a focus on tailormade and scalable solutions, we'll adapt our delivery style, communications and operations to suit the demands of the project, helping clients achieve their clinical and commercial objectives. Because our goal is the same as theirs; to improve patients' lives.
Summary of the Position:
We are looking for a Senior Project Manager to join our Project Management-Clinical Pharmacology department. You will be based remotely in the UK with an expectation to be at our offices in Merthyr Tydfil once a month or when needed.
You will provide leadership in managing multiple Clinical Pharmacology trials at Simbec-Orion. You will coordinate all trial activities across functional departments and vendors according to the Contract and scope of work and is accountable for the successful management and completion of assigned clinical trials. You will serve as the primary contact for the Sponsors to ensure that the study conduct and completion are progressing according to the Sponsors needs and expectations. You will ensure that clinical trials are conducted on time, on budget, according to SOPs, ICH- GCP and local regulations, in accordance with high-quality standards and contract specifications. You will lead and manage a team, providing coaching and mentoring and monitoring the team's workload.
Key Accountabilities:
Minimum Requirements:
Essential:
Desirable:
Simbec-Orion is an equal opportunity employer. Simbec-Orion will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law.
Simbec-Orion Job Profile - Senior Project Manager - Clin Pharm .docx
With a focus on tailormade and scalable solutions, we'll adapt our delivery style, communications and operations to suit the demands of the project, helping clients achieve their clinical and commercial objectives. Because our goal is the same as theirs; to improve patients' lives.
Summary of the Position:
We are looking for a Senior Project Manager to join our Project Management-Clinical Pharmacology department. You will be based remotely in the UK with an expectation to be at our offices in Merthyr Tydfil once a month or when needed.
You will provide leadership in managing multiple Clinical Pharmacology trials at Simbec-Orion. You will coordinate all trial activities across functional departments and vendors according to the Contract and scope of work and is accountable for the successful management and completion of assigned clinical trials. You will serve as the primary contact for the Sponsors to ensure that the study conduct and completion are progressing according to the Sponsors needs and expectations. You will ensure that clinical trials are conducted on time, on budget, according to SOPs, ICH- GCP and local regulations, in accordance with high-quality standards and contract specifications. You will lead and manage a team, providing coaching and mentoring and monitoring the team's workload.
Key Accountabilities:
- Manage projects in accordance with Good Clinical Practice (ICH-GCP), Standard Operating Procedures (SOPs), the UK Statutory Instrument No. 1031 (The Medicines for Human Use [Clinical Trials] Regulations 2004 and subsequent amendments) and applicable guidelines to meet Clients expectations.
- Advise on projects with clients, internal stakeholders and sub-contractors (including study design, feasibility, budgets and timeframes).
- Maintain awareness of current guidelines and advances in clinical research to support discussions with clients, internal stakeholders and sub-contractors.
- Ensure that appropriate resources are allocated at the appropriate times to ensure projects are delivered on schedule and within budget and keep all stakeholders informed of project progress.
- Prepare scientific and study documentation, including protocols (and subsequent amendments) and risk management plans.
- Act as a Line Manager providing guidance, coaching and mentoring to support the team's development.
- Participate in Commercial Development activities such as proposal development, review of budgets and Bid Defence meetings.
- Represent the Project Management department at internal and external meetings and deputise when required.
- Support in the generation of new SOPs and processes across the department.
- Deputise for other members of the Project Management team during absences.
Minimum Requirements:
Essential:
- BSc within a Life Science or overseas equivalent
- Previous experience of working within Project Management within Clinical Research
- Previous experience as a line manager
- Excellent organisation and time management skills with the ability to effectively manage any changes to priorities/deadlines.
- Excellent communication and negotiation skills with the ability to influence and communicate cross-functionally across all levels of seniority
- Ability to effectively lead a project team
- Logical and analytical thinker with good problem-solving skills.
- Experience in identifying, mitigating and managing project risks.
- English language - fluent, written & spoken.
Desirable:
- MSc or PhD in related discipline
- Formal project management qualification/certification
- Previous experience in Phase I trials
- Previous experience of deputising for Senior members of the team
Simbec-Orion is an equal opportunity employer. Simbec-Orion will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law.
Simbec-Orion Job Profile - Senior Project Manager - Clin Pharm .docx
Company
Learn more about this company
Visit this company’s hub to learn about their values, culture, and latest jobs.
Visit employer hub
You need to sign in or create an account to save a job.
Learn more about this company
Visit this company’s hub to learn about their values, culture, and latest jobs.
Visit employer hubGet job alerts
Create a job alert and receive personalised job recommendations straight to your inbox.
Create alert