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Director/Senior Director, Site Activation and Regulatory Therapeutic Lead (Remote/Europe)

Employer
Worldwide Clinical Trials
Location
HOMEWORKING, Nottingham, GB
Salary
Competitive
Start date
17 Sep 2020
Closing date
17 Oct 2020

View more

Discipline
Project Management
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Site Activation is a fast-growing, dynamic department! We are the launch pad for new projects. We help determine strategies for the optimal mix of countries, target sites, and other factors to expedite regulatory and recruitment objectives, and then we execute that strategy by initializing regulatory filings and locating, qualifying, and activating clinical research sites.

The Site Activation group is the perfect place to launch or further your career. We emphasize development of project management and strategic planning skills that will advance you though the opportunities within Site Activation or serve as an excellent pathway to advancement in Project Management or other Clinical Operations groups.

We are seeking an exceptional Director/Senior Director, Site Activation & Therapeutic Lead provides senior-level leadership and direction for all strategy development, operational planning, and delivery of global site contracting and regulatory affairs operations. Ensure that deliverables are done with high quality and consistent with sponsor contractual agreements. Standardizes and harmonize divisional processes to ensure consistency and improved efficiency. Responsible and accountable for the effective management of the operational, financial, and staff development activities of the Site Contracts and Regulatory Affairs divisions within the Site Activation department.

RESPONSIBILITIES:

Tasks may include but are not limited to:
  • Implement the short-term and long-term objectives, major plans and programs of the global Site Activation and Regulatory Affairs division through integrated strategies with functional service customers
  • Ensure alignment of divisional goals to enhance the achievement of corporate strategy and overall department objectives
  • Drive authorized plans and initiatives for the division ensuring they are properly implemented, and that Executive Leadership are informed of the overall trends and conditions of all important activities that impact profitability, market position or stature in the industry
  • Line management responsibilities for division leaders in Site Contracts and Regulatory Affairs. Responsible for interviewing and selection, team building, terminations, professional development, performance appraisals, job description preparation, and employee counseling.
  • Provide senior-level oversight for all deliverables for assigned projects, including implementation, quality, timelines, resource management, budget, and internal/external customer communications. Ensures all projects are managed and delivered in accordance with contractual agreements, agreed to Standard Operating Procedures, and in compliance with all industry/regulatory guidelines.
  • Develop and authorize specific performance standards to ensure key results in utilization, staff development, operating efficiency, innovation, physical and financial resources, public responsibility, and profitability for the Site Activation department.
  • Develop, review and maintain SOPs and best practice guidelines pertaining to activities of the Site Activation department. Identifies and makes recommendations of required technological and process improvements to increase quality and efficiency.
  • Review and input to budgets, assist with proposals and provide department representation at business development meetings

OTHER SKILLS AND ABILITIES:
  • Strong leadership skills
  • Excellent planning, strategizing, managing, monitoring, scheduling, and critiquing skills
  • Excellent written and verbal communication skills to clearly and concisely present information
  • Strong interpersonal skills in a fast-paced, deadline oriented, and changing environment

REQUIREMENTS:
  • Bachelor's Degree or equivalent education and experience.
  • At least 10 years experience within the function in CRO, pharmaceutical or other relevant area
  • At least 12 years management experience.
  • Proficiency in English
  • Proficiency with MS Word, Excel and Outlook

#LI-HD1

Company

Find out more about working for our company

Worldwide Clinical Trials -hub-button

Brief Company Description; 

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

 

Company info
Website
Mini-site
Worldwide Clinical Trials
Telephone
+44 115 956 7711
Location
1st Floor Waterfront House
Beeston Business Park
Beeston
Nottingham
Nottinghamshire
NG9 1LA
United Kingdom

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