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CDM PM (Veeva)

Thermo Fisher

CDM PM (Veeva)

Thermo Fisher

Bangalore, India

·

On-site

·

Full-time

·

2w ago

Required Skills

Project Management

Clinical Data Management

Veeva EDC

Leadership

Budget Management

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Data Manager Project Manager – 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 expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Clinical Data Manager Project Manager, you will act as a study manager for multiple studies individually or as a program of several studies. You may perform the Project Manager role for standalone studies. Your responsibilities will include functional, administrative, and financial oversight of assigned projects.

What You’ll Do:

  • Provide support and coaching to the DM team to ensure that all tasks are completed accurately, on time and within budget to meet or exceed client
  • expectations.
  • Act as a primary liaison for project team and client.
  • May develop and implement study specific training for DM project staff and performs independent reviews of DM deliverables following CDM guidelines.
  • Monitor, evaluate and propose mitigation strategies surrounding risk to deliverables and finances.
  • Participate in business development activities by assisting with bid preparation and representing data management at bid defense meetings, where required. Additionally, promote repeat business by developing relationships with new and existing clients.
  • Perform project forecasting of hours and identification of resource requirements and manage project budgets including identification of out of scope work and participate in the Contract Modification process.
  • Participate in the development and implementation of processes, procedures and training for the data management function as directed.
  • Mentor junior level staff and peers on all associated tasks within a study or program.
  • Independently lead and delegate tasks to ensure timely completion of project activities to project timelines, quality and budget.

Education and Experience Requirements:

  • • Bachelor's degree or equivalent and relevant formal academic / vocational qualification
  • • 8 Years of experience in Clinical Data Manager Role
  • Should have hands on working experience in Veeva EDC
  • Should have hands on working experience in Data Management- Project Management related Activities

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

  • Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations
  • Ability to use interactive computer programs
  • Excellent written/ verbal communication skills with a strong command of English language and grammar; strong organizational and analytical/problem solving skills; strong customer focus and excellent interpersonal skills
  • Ability to identify project risks and to effectively evaluate and develop plans to mitigate those risks
  • Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
  • Ability to act as a study or department expert for DM processes.
  • Ability to train and direct a study team, providing leadership and direction to both subordinates and peers
  • Ability to forecast project resourcing, project timeline planning and adherence to timelines.
  • Ability to supervise and delegate tasks.
  • Ability to successfully apply above skills, knowledge and abilities across a portfolio of studies

Working Conditions and Environment:

  • Work is performed in an office environment with exposure to electrical office equipment.
  • Occasional drives to site locations with occasional travel both domestic and international.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

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About Thermo Fisher

Thermo Fisher

Thermo Fisher Scientific Inc. is an American life science and clinical research company. It is a global supplier of analytical instruments, clinical development solutions, specialty diagnostics, laboratory, pharmaceutical and biotechnology services.

10,001+

Employees

Waltham

Headquarters

Reviews

3.9

2 reviews

Work Life Balance

3.5

Compensation

2.5

Culture

3.5

Career

4.0

Management

3.0

65%

Recommend to a Friend

Pros

Large company with extensive resources

Structured internship program

Career opportunities in product management

Cons

Low compensation ($22/hour)

High cost of living in location

Expensive housing/rent

Salary Ranges

2,260 data points

Mid/L4

Mid/L4 · Product Manager

168 reports

$130,313

total / year

Base

$120,231

Stock

-

Bonus

$10,082

$96,041

$178,720

Interview Experience

8 interviews

Difficulty

3.0

/ 5

Duration

14-28 weeks

Offer Rate

12%

Experience

Positive 12%

Neutral 63%

Negative 25%

Interview Process

1

Application Review

2

Recruiter Screen

3

Hiring Manager Interview

4

Panel Interview

5

Final Interview

6

Offer

Common Questions

Technical Knowledge

Behavioral/STAR

Past Experience

Culture Fit

Industry Specific