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Sr. Manager, CDM (FSP)

12-14 Years
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Job Description

Job Description :

Work Schedule

Second Shift (Afternoons)

Environmental Conditions

Office

Join Us as a Sr. Manager Clinical Data Management FSP- Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our FSP global team, you'll have the opportunity to manage a team of project staff and the workload of direct reports. As a Sr. Manager Clinical Data Management in FSP, you'll collaborate with leadership for training, mentoring, and guiding project staff and direct reports.

What You'll Do:


. Manages FSP staff, which may include interviewing and selection, job description preparation, professional development, goal setting, performance management, coaching and mentoring, employee counseling, and separations. Approves courses of action on salary administration, hiring, corrective action, and terminations. Reviews and approves time records, expense reports, requests for leave, and overtime.
. Provides support, oversight and coaching to the portfolio team to ensure that all tasks are completed accurately, on time and within budget to meet or exceed client expectations
. Manages resourcing (allocations) for all assigned staff, includes global resourcing reporting and strategizing with senior management.
. Ensures staff compliance with documented procedures.
. Assists with implementation of operational activities of study or portfolios, with focus on quality in order to better support study manager.
. Participates in the development and implementation of processes, procedures and training for the data management function.

Education and Experience Requirements:

  • Bachelor's degree or equivalent and relevant formal academic / vocational qualification
  • Previous experience that provides the knowledge, skills, and abilities to perform the job 12+ years
  • 5+ year of leadership responsibility
  • Strong working experience in operating FSP business model.
    Knowledge, Skills and Abilities:
    . Ability to effectively apply knowledge and skills in an organized fashion while adhering to regulatory guidelines, SOPs and client expectations
    . Good attention to detail and skill with numbers
    . Good written and verbal communication skills with good command of English language and grammar
    . Good analytical/problem-solving skills
    . Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
    . Good interpersonal skills
    . Ability to act as a study expert for DM processes
    . Ability to effectively manage and motivate others and to effectively supervise and delegate tasks
    . Ability to set and meet, for self and team, timelines or be able to recognize and schedule changes in response to project demands

We are hiring a team in India to support our FSP client - a large, globally recognized biopharmaceutical organization with a strong legacy in specialty medicines, vaccines, and scientific innovation. This sponsor is known for its commitment to patients, global research and development, and long-term investment in science. As a client dedicated FSP employee, you will collaborate with our client's global data science team, contribute to complex and high visibility initiatives, and work within a mature FSP delivery model focused on quality and partnership

Why You'll Want to Join:

  • Join our FSP Data Management team and help bring lifechanging medicines to patients worldwide. Accelerate your growth with handson experience in modern CDM, from EDC and data quality to AIenabled workflows-building the expertise to lead datadriven study delivery in a rapidly evolving clinical landscape
  • Global exposure:

Work on international clinical studies across phases and therapeutic areas, partner with global teams, CROs, vendors, and country operations.

  • End-to-end ownership:

Contribute to every stage of study delivery, from set-up to close-out.

  • Analytical & project skills:

Strengthen global project management, financial tracking, data analysis, and risk management abilities. Learn new clinical trial technologies like AI platforms to conduct a global clinical trial

About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, improving patient diagnostics and therapies or making their laboratory work more efficient, we are here to support them. Our distributed team of more than 90,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit. Thermo Fisher Scientific is a Equal employment opportunity

More Info

About Company

Thermo Fisher Scientific Inc. is an American supplier of scientific instrumentation, reagents and consumables, and software services. Based in Waltham, Massachusetts, Thermo Fisher was formed through the merger of Thermo Electron and Fisher Scientific in 2006. Thermo Fisher Scientific has acquired other reagent, consumable, instrumentation, and service providers, including: Life Technologies Corporation (2013), Alfa Aesar (2015),Affymetrix (2016),FEI Company (2016), BD Advanced Bioprocessing (2018),and PPD (2021).
As of 2017, the company had a market capitalization of $21 billion and was a Fortune 500 company. Annual revenue in 2021 was US$39.21 billion.
In March 2020, Thermo Fisher Scientific received emergency use authorization from the FDA for a test for SARS-CoV-2 to help mitigate the COVID-19 pandemic.

Job ID: 136758861

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