助理总监,数据科学、安全与监管FSP销售
Associate Director, Data Sciences, Safety, and Regulatory FSP Sales
职位名称:数据科学、安全与法规FSP销售高级经理
工作地点:北卡罗来纳州达勒姆,美国
工作地点类型:远程办公
工作合同类型:全职
职位级别:
申请此职位的候选人必须居住在该职位所在国家。
高级经理,数据科学、安全与法规,FSP销售
高级经理,数据科学、安全与法规,FSP销售将参与销售部门的一个重要部分——数据管理、生物统计学、编程、医学写作、生命周期安全和法规事务职能的FSP服务,并负责在多个客户账户中实现销售和增长目标。
核心职责包括:
- 与IQVIA传统客户群体以及非传统/新客户和市场建立关系,并积极寻找潜在的新业务机会。
- 与客户团队中的关键决策者建立关系,并深入了解客户的组织结构。
- 识别并回应客户需求,定义潜在机会,并向客户提供适当的策略/解决方案。
- 与全球业务运营部门协作,制定提案和合同。
- 保持对IQVIA专业FSP产品的深入了解,并在整个销售周期中提供“最佳实践”建议和解决方案。
- 维护客户、提案和合同数据库/跟踪系统。
- 及时处理来自内部和外部客户的咨询和信息请求。
- 建立IQVIA在专业FSP领域的竞争优势知识库,包括定位和定价、获奖或未获奖的具体原因、合同持续时间及状态等。
- 为指定客户的综合销售计划提供相关内容。
- 保持对IQVIA所有R&DS服务的一般了解,以寻找交叉销售机会,并跨公司各服务线与销售团队合作,交叉推广并响应RFP,同时建立内部关系以设计使用多种服务的解决方案。
- 通过参加、参与和在行业展会和会议上发言,支持销售和营销服务。
技能与能力:
- 必须具备出色的演示和
查看英文原文
Job Title: Associate Director, Data Sciences, Safety, and Regulatory FSP Sales
Job Location: Durham, North Carolina, United States of America
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
To be eligible for this position, you must reside in the same country where the job is located.
Associate Director, Data Sciences, Safety, and Regulatory FSP Sales
Associate Director, Data Sciences, Safety, and Regulatory, FSP Sales will contribute to a major segment of the Sales organization – FSP services for the Data Management, Biostatistics, Programming, Medical Writing, Lifecycle Safety, and Regulatory Affairs functions - and will be responsible for achieving sales and growth objectives across multiple accounts.
Core responsibilities include:
- Developing relationships with both IQVIA traditional customer base and non-traditional/new customers and markets, and actively prospecting potential new business opportunities.
- Cultivating relationships with key decision-makers within Account Teams and developing in-depth knowledge of the customers' organizations.
- Identifying and responding to customer needs, defining potential opportunities, and proposing appropriate strategy/solution to customer.
- Coordinating with Global Business Operations on the development of proposals and contracts.
- Maintaining an advanced understanding of IQVIA’s specialized FSP offerings and providing “best practice” advice and solutions throughout sales cycle.
- Maintaining customer, proposal, and contract database/tracking systems.
- Managing customer inquiries and requests for information from both internal and external customers in a timely manner.
- Developing and maintaining knowledge bank of IQVIA's position vs competitors in the specialized FSP space, including positioning and pricing, specific reasons for awards and non-awards, duration of contractual engagements, and status.
- Contribution of relevant content to comprehensive sales plan for target accounts.
- Maintaining general knowledge of all IQVIA R&DS services for appropriate cross-sell opportunities and working across company's service lines and with sales teams to cross-promote and respond to RFPs as well as develop internal relationships needed to create solutions designed using multiple services.
- Support sales and marketing services by attending, participating, and speaking at trade shows and industry conferences.
Skills and abilities:
- Must have excellent presentation and writing skills, act with a sense of urgency, and be able to work both independently and within a team environment.
- Must have excellent verbal communication skills and be comfortable cold calling prospective clients.
- Must be revenue driven, knowledgeable, consultative, a problem solver, customer focused, creative, resourceful, and fast-moving.
Requirements:
- Bachelor's Degree
- 10 years related experience, including 3 years of relevant industry (CRO/Pharmaceutical) and/or sales experience Req Or
- Equivalent combination of education, training and experience Req
- General knowledge of the Clinical Development space, Clinical Research Organization (CRO) operations, are required.
- Sales experience in a Clinical Research Organization, BPO, or Clinical Staffing Agency is strongly preferred.
- Operational exposure or experience in any of the following Clinical Data Management, Biostatistics, Statistical Programming, Medical Writing, Lifecycle Safety or Regulatory Affairs field is preferred.
- 30% travel is required (based on location).
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $89,900.00 - $250,400.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
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Originally posted on Himalayas