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Principal Program Lead. Job in Upper Gwynedd, Pennsylvania, United States in Merck & Co., Inc.. Nelest.com
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Principal Program Lead

col-narrow-left   

Job ID:

22157

Location:

Upper Gwynedd, PA 

Job function:

Research & Development
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Posted:

03.05.2016

Employment Type:

Full time

Industry:

Healthcare / Pharma
col-wide   

Title:

Principal Program Lead

Job Description:

Description Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Responsible and accountable for the oversight and leadership of clinical program execution. Leads and directs teams in key program planning and resourcing, development and execution elements (e.g. program level overviews, issue escalation/mitigations, presentations at Sr. Management meetings, program level cross-functional meetings and governance, advisory meeting preparation).

Has overarching responsibilities and/or oversight of multiple clinical programs or disease areas or highly complex programs. Assists the Clinical Directors in scientific leadership/investigator initiatives including preparation of publications, meeting presentations, due diligence activities, etc. Provides input into strategic direction for program level and/or therapeutic aligned end-to-end activities (planning through post-approval). Ensures consistency across program elements.

Facilitates and collaborates with internal and external stakeholders in support of clinical program objectives. Builds talent and capabilities of team members through proactive coaching, mentoring and development opportunities. Includes management of direct reports including assignment of resources, professional development and performance management. Travel: Yes, 5 % of the Time Description Principal Program Lead-CLI004614 Description Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Responsible and accountable for the oversight and leadership of clinical program execution. Leads and directs teams in key program planning and resourcing, development and execution elements (e.g. program level overviews, issue escalation/mitigations, presentations at Sr. Management meetings, program level cross-functional meetings and governance, advisory meeting preparation).
Has overarching responsibilities and/or oversight of multiple clinical programs or disease areas or highly complex programs. Assists the Clinical Directors in scientific leadership/investigator initiatives including preparation of publications, meeting presentations, due diligence activities, etc. Provides input into strategic direction for program level and/or therapeutic aligned end-to-end activities (planning through post-approval). Ensures consistency across program elements.
Facilitates and collaborates with internal and external stakeholders in support of clinical program objectives. Builds talent and capabilities of team members through proactive coaching, mentoring and development opportunities. Includes management of direct reports including assignment of resources, professional development and performance management. Qualifications Education:
  • Degree in the Life Sciences or significant experience in clinical development (>,18 years)
  • Bachelor's degree with a minimum of 15 years', or MS with a minimum of 12 years', or PhD with a minimum of 6 years' relevant career experience.

Job Requirements:

Qualifications Education:
  • Degree in the Life Sciences or significant experience in clinical development (>,18 years)
  • Bachelor's degree with a minimum of 15 years', or MS with a minimum of 12 years', or PhD with a minimum of 6 years' relevant career experience.


Required:
  • Knowledge of Pharmaceutical and/or clinical drug development process from program planning to regulatory submission.
  • Understanding scientific process, as well as medical and statistical concepts.
  • Excellent oral (including presentation) and written communication, project management, and computer/database management skills.
  • Must be able to make independent, timely, data-driven and appropriate decisions.
  • Demonstrated project management skills with proven ability to lead cross-functional teams and individuals.
  • Ability to influence and collaborate internally as well as externally with partners and study-related vendors
  • Knowledge of GCP, ICH guidelines and regulatory requirements
  • Managerial experience


Preferred:
  • Early Development experience (Phase I / II)
  • Dengue disease scientific experience


Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com. Search Firm Representatives Please Read Carefully: Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster EEOC GINA Supplement? Merck is an equal opportunity employer, Minority/Female/Disability/Veteran - proudly embracing diversity in all of its manifestations.

Zip Code:

19446

Company Info
Merck & Co., Inc.

Kenilworth, NJ, United States

Phone:
Web Site: merck.com

Company Profile

Company Info


Merck & Co., Inc.
Kenilworth, NJ, United States
Phone:
Web Site: merck.com

Principal Program Lead

col-narrow-left   

Job ID:

22157

Location:

Upper Gwynedd, PA 

Job function:

Research & Development
col-narrow-right   

Posted:

03.05.2016

Employment Type:

Full time

Industry:

Healthcare / Pharma
col-wide   

Title:

Principal Program Lead

Job Description:

Description Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Responsible and accountable for the oversight and leadership of clinical program execution. Leads and directs teams in key program planning and resourcing, development and execution elements (e.g. program level overviews, issue escalation/mitigations, presentations at Sr. Management meetings, program level cross-functional meetings and governance, advisory meeting preparation).

Has overarching responsibilities and/or oversight of multiple clinical programs or disease areas or highly complex programs. Assists the Clinical Directors in scientific leadership/investigator initiatives including preparation of publications, meeting presentations, due diligence activities, etc. Provides input into strategic direction for program level and/or therapeutic aligned end-to-end activities (planning through post-approval). Ensures consistency across program elements.

Facilitates and collaborates with internal and external stakeholders in support of clinical program objectives. Builds talent and capabilities of team members through proactive coaching, mentoring and development opportunities. Includes management of direct reports including assignment of resources, professional development and performance management. Travel: Yes, 5 % of the Time Description Principal Program Lead-CLI004614 Description Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Responsible and accountable for the oversight and leadership of clinical program execution. Leads and directs teams in key program planning and resourcing, development and execution elements (e.g. program level overviews, issue escalation/mitigations, presentations at Sr. Management meetings, program level cross-functional meetings and governance, advisory meeting preparation).
Has overarching responsibilities and/or oversight of multiple clinical programs or disease areas or highly complex programs. Assists the Clinical Directors in scientific leadership/investigator initiatives including preparation of publications, meeting presentations, due diligence activities, etc. Provides input into strategic direction for program level and/or therapeutic aligned end-to-end activities (planning through post-approval). Ensures consistency across program elements.
Facilitates and collaborates with internal and external stakeholders in support of clinical program objectives. Builds talent and capabilities of team members through proactive coaching, mentoring and development opportunities. Includes management of direct reports including assignment of resources, professional development and performance management. Qualifications Education:
  • Degree in the Life Sciences or significant experience in clinical development (>,18 years)
  • Bachelor's degree with a minimum of 15 years', or MS with a minimum of 12 years', or PhD with a minimum of 6 years' relevant career experience.

Job Requirements:

Qualifications Education:
  • Degree in the Life Sciences or significant experience in clinical development (>,18 years)
  • Bachelor's degree with a minimum of 15 years', or MS with a minimum of 12 years', or PhD with a minimum of 6 years' relevant career experience.


Required:
  • Knowledge of Pharmaceutical and/or clinical drug development process from program planning to regulatory submission.
  • Understanding scientific process, as well as medical and statistical concepts.
  • Excellent oral (including presentation) and written communication, project management, and computer/database management skills.
  • Must be able to make independent, timely, data-driven and appropriate decisions.
  • Demonstrated project management skills with proven ability to lead cross-functional teams and individuals.
  • Ability to influence and collaborate internally as well as externally with partners and study-related vendors
  • Knowledge of GCP, ICH guidelines and regulatory requirements
  • Managerial experience


Preferred:
  • Early Development experience (Phase I / II)
  • Dengue disease scientific experience


Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com. Search Firm Representatives Please Read Carefully: Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. Visa sponsorship is not available for this position. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster EEOC GINA Supplement? Merck is an equal opportunity employer, Minority/Female/Disability/Veteran - proudly embracing diversity in all of its manifestations.

Zip Code:

19446
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