Job Description:
Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as 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 people 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 for the strategic design, planning, and implementation of clinical trial recruitment and retention across multiple therapeutic areas within the Clinical Development and Execution Organization.
- Communicate with clinical trial teams in a matrix environment to implement and monitor the impact of proposed tactics and serve as an expert consultant to make additional recommendations as needed based on study performance.
- Collaborate with internal teams and manage vendors to deliver specific tactics of recruitment/retention strategies.
- Represent Global Trial Optimization to present strategy/rationale, train CRAs and site staff, and conduct recruitment support workshops as required.
- May be assigned special projects as needed to enhance overall group deliverables.
Qualifications
Education Minimum Requirement:
- Bachelor's degree (preferred in life sciences, communications or marketing)
Required Experience and Skills:
- Minimum 5 years’ clinical development or related experience
- Prior experience with recruitment and retention of clinical subjects
- Strong interpersonal and communication skills
- In depth knowledge of the drug development processes across all functional areas
- Knowledge and ability to apply GCP / ICH and applicable regulatory guidelines
- Superior presentation skills
- Computer skills including proficiency in aspects of data analysis and presentation software, Microsoft Word, and Excel
- Excellent organizational and problem solving skills
- Effective time management skills and ability to manage competing priorities
- Ability to establish and maintain effective working relationships in a matrix environment
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. Merck’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 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.
ZZ5ML
Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.
Job: Clinical Research (Non-M.D.)
Job Title:Sr. Scientist, Clinical Research
Primary Location: NA-US-NJ-Rahway
Other Locations: NA-US-PA-Upper Gwynedd
Employee Status: Regular
Travel: Yes, 5 % of the Time
Number of Openings: 2
Additional Info:
[Click Here to Access the Original Job Post]
Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as 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 people 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 for the strategic design, planning, and implementation of clinical trial recruitment and retention across multiple therapeutic areas within the Clinical Development and Execution Organization.
- Communicate with clinical trial teams in a matrix environment to implement and monitor the impact of proposed tactics and serve as an expert consultant to make additional recommendations as needed based on study performance.
- Collaborate with internal teams and manage vendors to deliver specific tactics of recruitment/retention strategies.
- Represent Global Trial Optimization to present strategy/rationale, train CRAs and site staff, and conduct recruitment support workshops as required.
- May be assigned special projects as needed to enhance overall group deliverables.
Qualifications
Education Minimum Requirement:
- Bachelor's degree (preferred in life sciences, communications or marketing)
Required Experience and Skills:
- Minimum 5 years’ clinical development or related experience
- Prior experience with recruitment and retention of clinical subjects
- Strong interpersonal and communication skills
- In depth knowledge of the drug development processes across all functional areas
- Knowledge and ability to apply GCP / ICH and applicable regulatory guidelines
- Superior presentation skills
- Computer skills including proficiency in aspects of data analysis and presentation software, Microsoft Word, and Excel
- Excellent organizational and problem solving skills
- Effective time management skills and ability to manage competing priorities
- Ability to establish and maintain effective working relationships in a matrix environment
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. Merck’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 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.
ZZ5ML
Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.
Job: Clinical Research (Non-M.D.)
Job Title:Sr. Scientist, Clinical Research
Primary Location: NA-US-NJ-Rahway
Other Locations: NA-US-PA-Upper Gwynedd
Employee Status: Regular
Travel: Yes, 5 % of the Time
Number of Openings: 2
Requeriments :
Skills :
Areas :
Additional Info:
[Click Here to Access the Original Job Post]