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Global Feasibility Lead

3+ years
Not Disclosed
10 Dec. 5, 2024
Job Description
Job Type: Full Time Education: BS/BA Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Global Feasibility Lead, SSU and Regulatory

Location: India-Asia Pacific - Home-Based, India
Job ID: 24006279
Posted: November 29, 2024

About Syneos Health
Syneos Health® is a global, fully integrated biopharmaceutical solutions company designed to accelerate customer success. We combine clinical, medical affairs, and commercial insights to deliver impactful outcomes in today's complex healthcare landscape. Our Clinical Development model places customers and patients at the heart of everything we do. We're committed to simplifying and streamlining processes to make Syneos Health a great partner to work with and an even better place to work for.

Join us in a collaborative environment where passionate professionals innovate together to achieve our customers' goals. We are driven by a common passion to accelerate therapies and change lives.

Why Syneos Health?

We foster career growth and development, offering mentorship, training, and recognition programs. Our Total Self culture emphasizes being your authentic self, where diversity in thought and background strengthens our global workforce. We’re continuously building the company we all want to work for, creating an inclusive environment where everyone feels they belong.


Job Responsibilities

  • Lead Feasibility Assessments: Take charge of Request for Proposal (RFP) and standalone feasibility assessments, ensuring thorough analysis and proposing approaches for optimal results.
  • Independently Manage Projects: Handle multiple assignments and manage the complexity of tasks related to pre-award site-level feasibility assessments, ensuring high-quality outputs with minimal oversight.
  • Stakeholder Liaison: Collaborate with internal teams, including Business Units, Business Development, Medical Directors, and Business Analysts, to align on project requirements, protocols, and timelines for RFPs.
  • Research and Analysis: Conduct in-depth research using scientific literature, internal metrics, and tools to support feasibility assessments and inform project decisions.
  • Feasibility Reporting: Prepare written reports and presentations summarizing the results of feasibility studies for internal and external stakeholders.
  • Data Management: Assist in developing and maintaining systems for storing and analyzing historical feasibility data, ensuring smooth retrieval and sharing for current RFPs.
  • Process Improvement: Identify opportunities for process enhancement and contribute to the development of feasibility analysis systems.
  • Mentorship: Guide and mentor team members on complex requests and multi-study programs when necessary.

Qualifications

  • Educational Background: BS/BA in Science (preferably in medical research).
  • Experience: Minimum 3 years of experience in feasibility or clinical research, with proven ability to work independently in a virtual team setting.
  • Technical Skills: Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and internet research tools.
  • Industry Knowledge: Familiarity with clinical research, CRO industry standards, and the ability to understand and present scientific and clinical data.
  • Communication: Strong verbal and written communication skills, with the ability to prepare compelling bid texts and presentations.
  • Organizational Skills: Ability to manage multiple tasks, prioritize effectively, and meet deadlines in a fast-paced environment.
  • Mentoring Skills: Experience in mentoring team members and managing data to drive business objectives.
  • Travel: Willingness to travel up to 5% if required.

About Us

In the past 5 years, Syneos Health has worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products, and managed over 200 studies across 73,000 sites, impacting over 675,000 trial patients.

Join us at Syneos Health, where your role makes a difference.