天津招聘

Guidelines:
1. Role profiles should be created for all roles that require screening: new and overlapping roles.
2. The Role Profile below should be completed based on the job, not the individual who does or will fill that role.
3. Note that if there are like roles in other functions/affiliates, there should be a single, consoli-dated role profile to describe that role.


Role Profile: GLOBAL CLINICAL SITE DEVELOPMENT
General (organization chart to be attached)

Job Title: Associate Global Clinical Site Developer
Job Grade:
Department: CTM / Clinical Development / GCRA
Reports to (Job Title): Regional Clinical Site Development Manager, Asia & Russia

Job Purpose (State in one sentence the overall objective of the role)

The Associate Global Clinical Site Developer will be responsible for the identification, evaluation and selection of qualified primary investigators and sites for Alcon’s clinical trials. This is accomplished by working closely with representatives from multiple functions to identify needs for study sites, assess and track site performance, coordinate site allocation and create plans for site development. They provide expertise and knowledge assuring appropriate protocol feasibility, effective patient recruitment and retention plans and compliance with international guidelines, regulations and corporate policies and procedures.

Major Accountabilities (Describe the 5-7 main results of the role to be achieved )

1. Responsible for the site identification and evaluation processes for Alcon’s phases of clinical trials
2. Develops country feasibility and strategy for conducting clinical trials
3. Develops and supervises implementation of training strategy for sites and GCSM personnel
4. Implements and executes effective patient recruitment and retention plans
5. Ensures protocol feasibility and optimization processes for all studies
6. Builds relationship with scientific leaders in key markets


Key Performance Indicators (Indicate how performance for this role will be measured)

? No delays in study Start-up cycle time
o Selection of Sites prior to identified metric
o Patient Recruitment and Retention plans for all study sites
? Recruitment predictability
? Apropriate GCP training for all sites
? Development of Centers of Excellence
? No quality and/or complaince issues in all phases of clinical trials
? Standard and consistent processess and procedures across studies


Job Dimensions (Indicate key facts and figures)

Number of associates:
Direct reports: 0
Indirect Reports: 0
Financial responsibility:
Operating Budget: NA
Impact on the organization: ? Lead Change
? Develop Centers of Excellence
? Build effective relationships with key investigators and scientific leaders
? Ensure Compliance


Affiliate CFO
Background (State the required education, experience level, and competency profile)

Education : ? Bachelor's Degree in a medical or scientific discipline.
? Advanced degrees (e.g., MD, PhD., O.D., PharmD) are preferred
Languages: ? Fluency in English essential
? Knowledge/Fluency of at least one other language preferred (Russian is preferable)

Experience: ? Minimum of 10 years of Pharmaceutical/Medical Device industry experience
? At least 6 years of monitoring and/or site development experience.
? Previous leadership, training, and/or sales or marketing experience is desirable and may substitute for monitoring experience.

We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.